Jobs at Click Therapeutics
249,921 open positions
(Sr.) Bioinformatics Analyst
Company: Shape Therapeutics
Location: Seattle, WA
Posted Sep 21, 2023
Employees are eligible to enroll in our Company’s voluntary 401k plan, voluntary Life/AD&D and Voluntary FSA’s.The salary range for a Bioinformatics Analyst is $90,000-$115,000 and the salary range for a Sr. Bioinformatics Analyst is $100,000-$125,000. We are proud to offer a competitive paid parental leave benefit, an annual employee stipend for employees to use however they choose, a Flex Paid Time Off program (allowing flexible PTO for vacation, sick leave, and other purposes) and Company paid Long Term Disability. not only through our science, but also through our commitment to foster an inclusive environment that supports diverse perspectives and experiences. Additional compensation may include annual target bonus and/or sign-on bonus, equity grant and relocation bonus.We aspire to Shape Life! The successful candidate will have the unique opportunity to work closely with other computational and experimental scientists to help develop, implement, and refine our next-generation processing and analytical pipelines to develop the next generation of gene therapies for treating serious human diseases.Why join ShapeAI?Interdisciplinary Collaborations: Engage in high-level research across a broad range of scientific disciplines and departments.State-of-the-Art Technologies: Access to tremendous amounts of data generated from novel gene therapy platforms coupled with high-performance computing and generative ML infrastructure.Professional Growth: Strong mentorship from experienced computational scientists coupled with opportunities for training and career development.If the notion of building novel informatics solutions to help accelerate the development of gene therapies for millions suffering worldwide from rare genetic disorders motivates you as it does us, we’re very excited to have you join us! What You’ll Do: Develop, test, and deploy scalable bioinformatics and analytical pipelines that ingest and process multimodal high-throughput biological dataPartner with bench scientists to translate and incorporate experimental complexities into computational pipelines and workflowsWrite and maintain code consistent with best practices of software design: including testing, documentation, reproducibility, usability, and peer reviewRegularly engage with multiple scientific teams to ensure the adoption of tools and data-driven decision-makingWhat You Bring: Qualifications and Requirements:Bachelor’s or Master’s degree in Computational Biology, Statistics, Genomics, Bioinformatics or related fieldsExperience developing processing pipelines for raw next-generation sequencing (NGS) dataSkills and Experience:Proficiency in Python and experience with Linux/Unix environments and open-source bioinformatics tools and databasesExperience with collaborative development using version control systems (e.g., Git) and software development best practices (e.g., CI/CD, testing, code review)Experience using workflow management systems such as Snakemake, Nextflow, or CWL is preferredExposure to cloud computing environments, high-performance computing, and containerization technologies like AWS Batch and Docker is a plusAbility to effectively manage one’s time and prioritize tasks to enable multiple projectsExquisite attention to detail, organization, and proactive communicationCurious mindset and willingness to learn from and mentor othersAbility to work both independently and collaboratively in a team-science environmentAbility to think outside the box and tackle challenges with a problem-solving, can-do attitudeShapeTX offers a robust benefits package, including but not limited to: Medical, Dental and Vision coverage for employees and their eligible dependents. Position OverviewShapeTX is looking for an enthusiastic, collaborative, and motivated Bioinformatics Analyst to join our fast-growing Analytics and Informatics (AI) department. You can find us at shapetx.com and on LinkedIn and Twitter.At ShapeTX, we are a dynamic team of professionals who are dedicated and passionate about making cures a reality. Through diversity of thought, scientific knowledge, professional rigor and focus we are merging cutting-edge science with extensive drug development expertise to unlock cures to many debilitating diseases.Shape Therapeutics is headquartered in Seattle, Washington with a satellite site in Boston, Massachusetts. The ShapeTX platform enables pharma innovators to design treatments across a wide range of diseases, including rare genetic disorders as well as debilitating conditions, such as Alzheimer’s, Parkinson’s, and many more. The hired applicant's placement within the range is based on qualifications and professional experience.
Senior/Lead Product Designer
Company: Click Therapeutics
Location: New York City, NY
Posted Sep 20, 2023
Strong conceptual, visual, analytical, and problem-solving skills. Proficiency in design tools, such as Sketch, Abstract, and Adobe Creative Suite. Bachelor's degree in Design, User Interaction, or related field. Click Therapeutics will conduct interviews face-to-face over Zoom. Employment applicants requiring immigration sponsorship must disclose, when initial application for employment is made, whether or not they are legally authorized to work for Click Therapeutics in the U.S. and, if so, whether that authorization permits them to work in the job they seek. You are comfortable conveying design ideas via sketches, storyboards, high-fidelity mockups, prototypes, or animations. Competitive Salary with Annual Review | Cash Bonus | Stock Options | 5% 401(k) matching | Medical | Dental | Vision | Life Insurance | Voluntary Benefits | Unlimited PTO | Uber One | Nectar Rewards | One Medical | Fertility Support | Fitness Reimbursement | Bike Membership | Professional Development Stipend | Lunch Stipends | Parent Benefits | Industrious Workspaces | Commuter Subsidies | Flexible Work Arrangement | Choice of Mac or Windows | Sponsored Company Events | Office Snacks and Beverages | Much More...Equal Employment Opportunity:Click Therapeutics is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. All job postings will be listed on the Click Therapeutics official career page. The final base salary will be dependent upon skills, experience and location. If someone contacts you about a job or position that is not listed on the official career page, please contact the Click Therapeutics recruitment team at the contact information below.
Associate / Senior Associate, Competitive Intelligence and Strategy
Company: Entrada Therapeutics
Location: Boston, MA
Posted Sep 22, 2023
Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.Third Party Staffing AgenciesEntrada does not accept unsolicited resumes from any source other than directly from candidates. We value work life balance, you'll benefit from discretionary time off, paternity leave, and an excellent 401(k) package. Example workstreams include competitive monitoring and tracking, conference coverage, and strategy development. strongly preferred.1-2 years of relevant experience, preferably in an analytical role such as market research, equity research, or life sciences consulting.Direct experience synthesizing and communicating competitive insights from drug development programs and/or companies.Exceptional analytical skills combined with a broad understanding of the life sciences business and R&D process.Ability to create and present ideas effectively using Microsoft PowerPoint, Word, and Excel.Desire to work in a fast-paced, innovative, and collaborative environment.Ability to be a team player with a can-do attitude and a willingness to embrace new challenges and the flexibility to adjust course based on new findings and team inputs.Located in the Greater Boston Area.The PerksBy becoming a team member here at Entrada, you’ll have access to competitive health, dental, and vision coverage, as well as life insurance, and short term and long-term disability insurance. You will also be supporting various workstreams in Scientific Strategy and Business Strategy by performing analyses of market intelligence and building scientific and commercial assessments to drive recommendations.ResponsibilitiesSupport and drive competitive intelligence activities, including tracking, analyzing, synthesizing, and communicating competitive and market activities to internal stakeholders in a concise and timely mannerAttend relevant conferences to track industry activities and trends to inform internal decision making.Conduct profiling and analysis of scientific opportunities in new therapeutic areas and modalities for the design and development of intracellular biologics using the EEV platform.Gather and capture market data to support data-driven analyses, generate strategic insights, and communicate findings in an efficient manner.The NecessitiesAt Entrada, our passion for science, our devotion to patients and our values drive our behavior:Humanity - We genuinely care about patients and about one another.Tenacity - We are relentless and persistent in the pursuit of developing therapies for patients.Creativity - We are creative problem solvers.Collaboration - We are more than the sum of our parts.Curiosity - We have a growth mindset and push conventional thought and theory.To thrive on our team, you will need to come with:Bachelor of Science or Arts degree in life sciences (biology, biochemistry, chemistry, etc.) You love reading about and following innovative science, performing data-driven analyses, and contributing strategic insights. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. You bring to the table the combination of an inquisitive spirit, critical thinking, and analytical skills. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes. We also offer a generous transportation stipend to commute as you wish.
Head of People Operations
Company: Relay Therapeutics
Location: Cambridge
Posted Sep 21, 2023
We have built a world-class team of leading experts from each of these disciplines, and they are driven by a deep collaboration at every step of our drug discovery process. Our team is equal parts fearless and relentless, with a shared passion for working collaboratively in intellectually stimulating environments. If you’re excited by the challenge of putting protein motion at the heart of drug discovery and passionate about making a difference in the lives of patients, join us! This is a great opportunity for someone who wants to make an impact and cares deeply about getting medicines to patients in need. Your RoleSet and oversee the direction of the People Operations function in support of the strategic objectives of Relay Tx and the People team Provide strategic input and operational leadership in the design, implementation, administration, and communication of compensation, benefit, and equity plans, systems, programs, and policies Mentor and manage the People Operations team Build and foster partnerships with key stakeholders including Finance, Legal, Operations, IT, as well as external vendors and partners Ensure that we have the key systems and processes in place to provide a seamless employee experience from onboarding to offboarding Enable the People team to collect, analyze and provide timely, value added and impactful data to support business activities and decisionsSupport our compensation strategy and oversee our compensation administration in partnership with our Finance team Lead our benefits strategy and execution, including benefits design, ESPP and 401k administration, and broker management In partnership with Legal and Finance, ensure compliance with state and federal laws and regulations, inclusive of filings, reports, and audits Your BackgroundYou have experience working within the guidelines of a publicly traded company You know what a successful People Operations function looks like in a dynamic, scaling organization You have a track record of developing strong partnerships with key stakeholders and other leaders You have a reputation for being an effective leader who can energize and motivate your teams and develop your employees You have a meticulous attention to detail You are service oriented and have an employee-first mentality – you know what it means to be white glove You are a clear, candid, and concise communicator – whether in person, by phone/ email, or in front of an audience presenting Biotech experience a plus LI-AM1About Relay TherapeuticsRelay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process with the goal of bringing life-changing therapies to patients. This “hands-on” leader will partner closely with leaders in Finance, Legal, IT, and Operations to oversee companywide programs and initiatives related to People Operations. We are seeking an experienced and versatile People Operations leader who will lead our dynamic People Operations function. This position provides leadership and strategic direction to the People Operations function. Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology. Our Dynamo platform integrates an array of leading-edge experimental and computational approaches to provide a differentiated understanding of protein structure and motion to drug these targets. The OpportunityRelay Tx is advancing a&8239;broad&8239;pipeline of promising&8239;precision medicines developed via our Dynamo platform and changing the way drugs are discovered along the way. Through unparalleled insights into protein motion, we are able to develop highly selective drugs against important disease drivers.
Project Director - Capital Projects
Company: Spark Therapeutics, Inc.
Location: Philadelphia, PA
Posted Sep 20, 2023
Internal and External Contacts Accountable to all business units requiring capital projects Internal Contacts - QC, QA, Facilities, Manufacturing, Supply Chain, MS&T, Finance, R&D External Contacts - Vendor ecosystem for designing, building and starting up Greenfield GMP /Clinical manufacturing and research laboratory facilities. Experience in Regulatory Inspections, Good Manufacturing Practice (GMP), Change Control, Validation aspects of major capital projects. Adept at managing Architectural/Engineering, Construction Management, and key Equipment supplier teams/resources and translating user requirements into actual conceptual, basic and detailed design. Have managed large capital projects through the entire capital project management lifecycle from Concept Design through Construction, Commissioning, Qualification and Start-Up. Key Skills, Abilities, and Competencies Multiple examples of proven results showing day to day efforts managing large, complex Capital Projects and build ahigh performance team for major capital projects. Experience utilizing Cost Control methodologies and firms to manage the overall project cost for the project. Collaborate with numerous cross functional teams within the Spark Technology Development Organization (Manufacturing, Digital Systems, MS&T, Process Development, and Quality) to ensure all facility and process assets are ideated, evaluated and selected, approved, constructed, delivered and supported in accordance to Spark IT principles, policies and standards. Demonstrated technical senior level project management experience to develop project goals, budgets, deliverables and timelines on large capital projects up to $200M and demonstrated ability to deliver on all aspects of Scope/Cost/Schedule. Strong team diagnostic skill and strategy for team growth. Develop, manage and maintain up-to-date project timelines inclusive of all critical milestones, key interdependencies and resource constraints, applying appropriate project scheduling techniques utilizing P6 scheduling tool.
(Sr.) Bioinformatics Associate Scientist
Company: Shape Therapeutics
Location: Seattle, WA
Posted Sep 21, 2023
Employees are eligible to enroll in our Company’s voluntary 401k plan, voluntary Life/AD&D and Voluntary FSA’s.The salary range for a Bioinformatics Associate Scientist is $105,000-$140,000 and the salary range for a Sr. Bioinformatics Associate Scientist is $110,000-$155,000. We are proud to offer a competitive paid parental leave benefit, an annual employee stipend for employees to use however they choose, a Flex Paid Time Off program (allowing flexible PTO for vacation, sick leave, and other purposes) and Company paid Long Term Disability. not only through our science, but also through our commitment to foster an inclusive environment that supports diverse perspectives and experiences. Additional compensation may include annual target bonus and/or sign-on bonus, equity grant and relocation bonus.We aspire to Shape Life! The successful candidate will have the unique opportunity to work closely with other computational and experimental scientists to help develop, implement, and refine our next-generation processing and analytical pipelines to develop the next generation of gene therapies for treating serious human diseases. Why join ShapeAI?Interdisciplinary Collaborations: Engage in high-level research across a broad range of scientific disciplines and departments.State-of-the-Art Technologies: Access to tremendous amounts of data generated from novel gene therapy platforms coupled with high-performance computing and generative ML infrastructure.Professional Growth: Strong mentorship from experienced computational scientists coupled with opportunities for training and career development.If the notion of building novel informatics solutions to help accelerate the development of gene therapies for millions suffering worldwide from rare genetic disorders motivates you as it does us, we’re very excited to have you join us! What You’ll Do: Design and implement reproducible methods for processing NGS data, laying the groundwork for statistical and machine learning (ML) analyses that rigorously test biological hypothesesInterface with experimentalists to ensure fidelity across experimental and computational methods developmentDevelop and maintain codebases using software design best practices: including testing, documentation, reproducibility, usability, and peer reviewCollaborate with diverse project teams to ensure the adoption of appropriate tools and analyses to inform decisionsWhat You Bring: Qualifications and Requirements:Bachelor’s degree with relevant work experience or Master’s degree in Computational Biology, Statistics, Genomics, Bioinformatics, or a related discipline.Proven experience developing processing pipelines for raw next-generation sequencing (NGS) dataSkills and Experience:Strong track record of developing and applying innovative and rigorous computational methodologies to high-throughput biological dataProficiency in Python and experience with Linux/Unix and open-source bioinformatics tools and databasesExperience with collaborative development using version control systems (e.g., Git) and software development best practices (e.g., CI/CD, testing, code review)Experience using workflow management systems (e.g., Nextflow, Snakemake, CWL) preferredExposure to cloud computing environments, high-performance computing, and containerization technologies (e.g., AWS Batch, SGE/SLURM, Docker)Experience in molecular biology and experimental design of -omic assays is a plusAbility to effectively manage one’s time and prioritize tasks to enable multiple projectsExquisite attention to detail, organization, and proactive communicationCurious mindset and willingness to learn from and mentor othersAbility to work both independently and collaboratively in a team-science environmentAbility to take initiative to think outside the box and tackle challenges with a problem-solving, can-do attitudeShapeTX offers a robust benefits package, including but not limited to: Medical, Dental and Vision coverage for employees and their eligible dependents. Position OverviewShapeTX is looking for an enthusiastic, collaborative, and motivated Bioinformatics Associate Scientist to join our fast-growing Analytics and Informatics (AI) department. You can find us at shapetx.com and on LinkedIn and Twitter.At ShapeTX, we are a dynamic team of professionals who are dedicated and passionate about making cures a reality. Through diversity of thought, scientific knowledge, professional rigor and focus we are merging cutting-edge science with extensive drug development expertise to unlock cures to many debilitating diseases.Shape Therapeutics is headquartered in Seattle, Washington with a satellite site in Boston, Massachusetts. The ShapeTX platform enables pharma innovators to design treatments across a wide range of diseases, including rare genetic disorders as well as debilitating conditions, such as Alzheimer’s, Parkinson’s, and many more. The hired applicant's placement within the range is based on qualifications and professional experience.
Project Director - Capital Projects
Company: Spark Therapeutics, Inc.
Location: Philadelphia, PA
Posted Sep 20, 2023
Internal and External Contacts Accountable to all business units requiring capital projects Internal Contacts - QC, QA, Facilities, Manufacturing, Supply Chain, MS&T, Finance, R&D External Contacts - Vendor ecosystem for designing, building and starting up Greenfield GMP /Clinical manufacturing and research laboratory facilities. Experience in Regulatory Inspections, Good Manufacturing Practice (GMP), Change Control, Validation aspects of major capital projects. Adept at managing Architectural/Engineering, Construction Management, and key Equipment supplier teams/resources and translating user requirements into actual conceptual, basic and detailed design. Have managed large capital projects through the entire capital project management lifecycle from Concept Design through Construction, Commissioning, Qualification and Start-Up. Key Skills, Abilities, and Competencies Multiple examples of proven results showing day to day efforts managing large, complex Capital Projects and build ahigh performance team for major capital projects. Experience utilizing Cost Control methodologies and firms to manage the overall project cost for the project. 25% Collaborate with numerous cross functional teams within the Spark Technology Development Organization (Manufacturing, Digital Systems, MS&T, Process Development, and Quality) to ensure all facility and process assets are ideated, evaluated and selected, approved, constructed, delivered and supported in accordance to Spark IT principles, policies and standards. Demonstrated technical senior level project management experience to develop project goals, budgets, deliverables and timelines on large capital projects up to $200M and demonstrated ability to deliver on all aspects of Scope/Cost/Schedule. Strong team diagnostic skill and strategy for team growth. Develop, manage and maintain up-to-date project timelines inclusive of all critical milestones, key interdependencies and resource constraints, applying appropriate project scheduling techniques utilizing P6 scheduling tool.
Senior Accountant
Company: Dyne Therapeutics
Location: Waltham
Posted Sep 20, 2023
All Employees are expected to adhere to all company policies and act as a role model for company values.Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. For more information, please visit https://www.dyne-tx.com/, and follow us on Twitter, LinkedIn and Facebook.Role Summary:The Senior Accountant supports the finance team in day-to-day operations and department-wide projects and is integral to the monthly close process, including reconciliations and journal entries. This position may change or assume additional duties at any time. The employee may be requested to perform different or additional duties as assigned. This role is based in Waltham, MA without the possibility of being a remote role. Primary Responsibilities Include:Accounts payable process including payment runs and vendor communicationDrive the monthly closing process and prepare account reconciliationsWork cross functionally to track monthly accrualsAnalyze monthly variances across accounts and investigate discrepancies as neededProcess payroll accurately and timelyOwn employee expense reporting and reimbursementGeneral ledger / ERP implementation and maintenanceSupport quarterly reviews and annual audit process with external auditorsAssist in establishing and enforcing proper accounting methods, policies and principlesSupport management and cross functional teams through ad-hoc reporting, analysis and special projects, and employee experience initiativesWork with various business providers to identify and implement appropriate software solutions for a high-growth company Education and Skill Requirements:Minimum of a Bachelor’s degree in Accounting or similar field is requiredCPA is preferred but not requiredMinimum of 3-5+ years of progressive accounting experience with a minimum of 2 years’ experience in a public company environment - Life Science industry experience is strongly preferredSolid knowledge of U.S. GAAP and SOXHighly detail-oriented and exceptionally organized; accountable to immediate team and internal stakeholdersAbility to work collaboratively across departmental functions and build key external relationshipsExcellent communication skills both written and verbal are mandatoryAbility to manage and complete projects with time constraintsAbility to successfully work independently and within a team environmentLI-OnlineThe statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. This role works independently in a fast-paced environment, has public company reporting experience and embraces a team mentality to support the entire organization. This role reports to the Corporate Controller or his/her designee. Dyne has a broad pipeline for serious muscle diseases, including clinical programs for myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD), and a preclinical program for facioscapulohumeral muscular dystrophy (FSHD). With its proprietary FORCE™ platform, Dyne is developing modern oligonucleotide therapeutics that are designed to overcome limitations in delivery to muscle tissue. Company Overview:Dyne Therapeutics is a clinical-stage muscle disease company focused on advancing innovative life-transforming therapeutics for people living with genetically driven diseases.
Director/Associate Director, Supply Chain
Company: Corcept Therapeutics
Location: Peninsula
Posted Sep 20, 2023
Today, we have a unique opportunity to revolutionize the treatment of severe endocrine, oncology, metabolism and neurology disorders and aim to deliver better outcomes for the people affected by them.This position will provide leadership in the planning, forecasting, materials sourcing, distribution and return of Corcept’s development and commercial products.Responsibilities: Identify and manage external global partners (e.g., depot, affiliate ops, CRO, IxRS vendors) to ensure consistent availability of drug supply at distribution centers/clinical trial sitesDevelop, maintain, and implement supply chain policies, procedures, techniques, standards, and systems with a focus on continuous improvementCoordinates labeling; defines packaging requirements; controls inventory; oversees shipping/receiving (including import/export), storage, and destructionGenerate and review documents such as work orders, contracts, purchase orders, material transfer requests, and shipping documentationWorks with QA to ensure supplies are prepared in accordance with the applicable global GxP regulations; supports QA vendor qualification and auditing processNegotiate contracts with suppliers/vendors to secure best pricing for the business. An annual cash bonus and equity grants may be provided as part of the overall compensation package, in addition to a full range of medical, financial, and/or other wellness benefits, dependent on the position offered. Applicants must be currently authorized to work in the United States on a full-time basis.If you are based in California, we encourage you to read this important information for California residents linked here.Corcept appreciates the commitment and hard work of all our team members as we strive to discover and develop novel treatments for patients with serious unmet medical needs. Please visit our website at: https://www.corcept.com/Corcept is an Equal Opportunity Employer Manage budgets and collaborate with Finance to address budget variance.Lead Supply meetingsPosition requires 10-15% travelPreferred Skills, Qualifications and Technical Proficiencies: Demonstrated knowledge of forecasting and inventory management as it relates to master scheduling, materials requirement planning, and applicable SOPs and GMPsAbility to think strategically in order to anticipate risk to uninterrupted supplyDemonstrated skill in successful international shipment, including customs clearanceDemonstrated ability to establish supply strategy from clinical drug protocolPreferred Education and Experience: Bachelor of Science degree in Life Sciences or Business (Operations Management or Supply Chain Management) or equivalent experience; certifications such as APICS, CPIM, CIRM, PMP are preferred10+ years’ experience in pharmaceutical industry, 7+ years experience in supply chainExperience in management of IRT systemsThe pay range that the Company reasonably expects to pay for this position is $190,000 - $231,600; the pay ultimately offered may vary based on legitimate considerations, including job-related knowledge, skills, experience, and education. Our vibrant community is made up of over 300 people—medical practitioners, scientists, and industry professionals—all with the shared goal of advancing the science of cortisol modulation to treat serious disease.Our work has uncovered over 1000 proprietary selective cortisol modulators, including our marketed product, Korlym® (mifepristone), the first treatment available for those living with Cushing’s syndrome, a life-threatening condition caused by excess cortisol activity. Monitor and report the cost, schedules and performance aspects of contracts, ensuring budgets and timelines are on trackAssist with the preparation of the department budget. That is why for twenty-five years we have pushed the boundaries of what is possible, driven by fiercely independent science, open collaboration and the curiosity to follow the data wherever it leads.Our company is committed to building a culture that values diverse perspectives and the unique contributions of every employee. At Corcept Therapeutics, we believe the potential impact of cortisol modulation on the future of health has long gone overlooked.
Senior Product Manager
Company: Click Therapeutics
Location: New York City, NY
Posted Sep 20, 2023
Experience working with technologies including, but not limited to, ReactNative, Node.js, AWS. Strong technical leadership, project management, analytical problem solving, business analysis, and troubleshooting skills. Click Therapeutics will conduct interviews face-to-face over Zoom. Employment applicants requiring immigration sponsorship must disclose, when initial application for employment is made, whether or not they are legally authorized to work for Click Therapeutics in the U.S. and, if so, whether that authorization permits them to work in the job they seek. Background or previous experience in neuroscience, psychiatry, psychology, behavior change, digital health or a related field. Experience conducting clinical research. Competitive Salary with Annual Review | Cash Bonus | Stock Options | 5% 401(k) matching | Medical | Dental | Vision | Life Insurance | Voluntary Benefits | Unlimited PTO | Uber One | Nectar Rewards | One Medical | Fertility Support | Fitness Reimbursement | Bike Membership | Professional Development Stipend | Lunch Stipends | Parent Benefits | Industrious Workspaces | Commuter Subsidies | Flexible Work Arrangement | Choice of Mac or Windows | Sponsored Company Events | Office Snacks and Beverages | Much More...Equal Employment Opportunity:Click Therapeutics is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. All job postings will be listed on the Click Therapeutics official career page. The final base salary will be dependent upon skills, experience and location. If someone contacts you about a job or position that is not listed on the official career page, please contact the Click Therapeutics recruitment team at the contact information below.
Senior Scientist, Bioanalytical
Company: Entrada Therapeutics
Location: Boston, MA
Posted Sep 21, 2023
Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.Third Party Staffing AgenciesEntrada does not accept unsolicited resumes from any source other than directly from candidates. We value work life balance, you'll benefit from discretionary time off, paternity leave, and an excellent 401(k) package. Experience with managing direct reports is required.Subject matter expert with extensive hands-on experience developing, qualifying, and validating LC-MS/MS-based bioanalytical assays to support a variety of modalities including oligonucelotides, biologics, and peptides.In-depth knowledge and strong experience with assay development, transfer, qualification, and validation to external CROs in a GLP/GxP environment.Ability to work independently in a fast-paced environment, as well as in a cross-collaborative team setting. Excellent communication skills (oral and written) and a track record of cross-disciplinary collaboration.Knowledge/experience of pharmacokinetics, drug metabolism, immunogenicity and biomarker studies are highly desirable.Experience with ligand binding assays such as ELISA and MSD is preferred.The PerksBy becoming a team member here at Entrada, you’ll have access to competitive health, dental, and vision coverage, as well as life insurance, and short term and long-term disability insurance. You work successfully in a team environment with strong interpersonal skills to effectively build working relationships inside and outside the company.The OpportunityWork within the bioanalytical team to enable the full spectrum of EEV-conjugated modalities development from early discovery candidate selection through late-stage process development.ResponsibilitiesDevelop, qualify, and implement bioanalytical methods supporting PK and biodistribution using LC-MS/MS and ligand binding assays to support EEV-conjugated therapeutics including oligonucleotides, biologics, and peptides.Perform hands-on method development and sample analysis support and manage a team of scientists to supporting non-GLP studies (PK) in various biological matrices (plasma, CSF, urine, and tissues, etc.). You have excellent verbal and written communication skills, you follow up and follow through, bringing solutions to problems efficiently. Create high-quality data and reports in a timely manner to meet timeline deliverables.Oversee non-GLP and GLP bioanalytical activities at CRO partners; provide scientific guidance and technical support on method transfer/development, qualification/validation, and sample analysis at CROs.Evaluate and implement new and upcoming technologies/platforms outside field of expertise to meet challenging program needs.Mentor and train scientists/associates on scientific concepts and technical details of various bioanalytical approaches, as well as regulatory requirements in a GLP/GxP environment.Implement processes to ensure both internal and external timelines are met with data integrity and good documentation practice, communicate and interface with stakeholders including discovery, preclinical, CMC, and clinical team and external CROs to define and deliver strategies to support project timelines across multiple programs.Write and review protocols and bioanalytical sections to be included in regulatory filings; act as a SME in the Bioanalytical group for GLP/GxP regulations and health authority guidances.The NecessitiesAt Entrada, our passion for science, our devotion to patients and our values drive our behavior:Humanity - We genuinely care about patients and about one another.Tenacity - We are relentless and persistent in the pursuit of developing therapies for patients.Creativity - We are creative problem solvers.Collaboration - We are more than the sum of our parts.Curiosity - We have a growth mindset and push conventional thought and theory.To thrive on our team, you will need to come with:PhD in chemistry, biochemistry, pharmacology, analytical chemistry, or a related field with 4-6 years of post-doctoral experience; or a master’s degree with 8+ years of experience.Demonstrated leadership and project management/organizational skills. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. You will successfully lead and coordinate bioanalytical support functions across various modalities, including oligonucleotide and biologics modalities, to perform quantitative bioanalysis in complex biological matrices, and to actively explore, investigate and implement innovative technologies to facilitate program progress. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes.
Scientist, Translational Sciences (In Vitro)
Company: Entrada Therapeutics
Location: Boston, MA
Posted Sep 22, 2023
), ELISA, rt-PCR, dd-PCR, Western blot, cell-based assays, etc. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.Third Party Staffing AgenciesEntrada does not accept unsolicited resumes from any source other than directly from candidates. analysis testing in vitro samples including a broad range of techniques including RT-PCR, ddPCR, Western blot, ELISA, etc. We value work life balance, you'll benefit from discretionary time off, paternity leave, and an excellent 401(k) package. Muscle cell culture experience is a good plus. A translational team member experience in an industry setting for assets progressing through IND-enabling studies is a good plus The PerksBy becoming a team member here at Entrada, you’ll have access to competitive health, dental, and vision coverage, as well as life insurance, and short term and long-term disability insurance. Lead and/or support in vitro study designs for non-clinical pharmacological efficacious readouts, mechanism of action-related translational questions, and pharmacodynamic and pharmacokinetic relationships of the clinical candidate. Collaborate with discovery and support the Biomarker team for writing and following standard operating procedures and biomarker analysis method transfer and method qualification. Contribute to authoring and review (technical and data QC) of internal stage-gate documents for regulatory and/or discovery purposes. Work with team members in preclinical stage project teams to produce clear, testable translational hypotheses to address program objectives. The NecessitiesAt Entrada, our passion for science, our devotion to patients and our values drive our behavior:Humanity - We genuinely care about patients and about one another.Tenacity - We are relentless and persistent in the pursuit of developing therapies for patients.Creativity - We are creative problem solvers.Collaboration - We are more than the sum of our parts.Curiosity - We have a growth mindset and push conventional thought and theory.To thrive on our team, you will need to come with:PhD degree in a scientific discipline with 0-2 years of industry/post-doctoral experience for a Scientist I and 2-4 years of industry/post-doctoral experience for a Scientist II Excellent oral and written communication skills, including writing, reviewing, and editing scientific documents Work and drive decision-making within a versatile, multi-regional, and matrix teams Right attitude (agile, curious, open-minded, "can-do" mindset) Ability to be scientifically independent and manage workload and expectations Preferred experience Track record of success and measurable contribution in moving any therapeutic programs forward through preclinical and clinical development in an academic or industry setting Experience in research of oligo, biologics (antibody or enzymes), and other moiety-based therapies is a good plus (small molecules, CGT, etc) Hands on experiences on analysis including binding affinity (BLI, SPR, etc. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Job title will be commensurate on the experience of the candidate. The OpportunityAs an In Vitro Translational Scientist in the Product Development Group, you will join the Product Development Team and support projects as they move through drug discovery and into early clinical development. You follow up and follow through, and efficiently bring solutions to problems.