Jobs at Click Therapeutics
249,921 open positions
Scientist, Regulated Bioanalysis
Company: Spark Therapeutics, Inc.
Location: Philadelphia, PA
Posted Oct 17, 2023
Spark Therapeutics is seeking a scientist with a Ph.D. or M.S. in Immunology, Cell Biology, or related fields, with 2+ years or 5+ years of experience respectively, or a B.S. with 8-10+ years of experience. The candidate will join the Neutralization Assay Team, conducting cell-based and other neutralization assays for gene therapy programs. They will develop and validate assays, analyze data, and author reports. The role involves working in a regulated environment, collaborating with inter-departmental partners, and staying updated with scientific advancements. The base salary range is from $100,200 to $150,400.
Senior Scientist, Bioanalytical
Company: Entrada Therapeutics
Location: Boston, MA
Posted Oct 16, 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. 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. 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. 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 Oct 17, 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. You follow up and follow through, and efficiently bring solutions to problems. 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.
Senior/Lead Product Designer
Company: Click Therapeutics
Location: New York City, NY
Posted Oct 15, 2023
Click Therapeutics is seeking a Senior/Lead Product Designer with 5+ years of experience in designing consumer-facing mobile applications. The role involves leading the design of products throughout the entire lifecycle, collaborating with cross-functional teams, and ensuring exceptional patient experiences. The position is based in Tribeca, NYC, with a hybrid working model. The company offers a competitive salary, annual performance-based cash bonus, and a generous equity package, along with comprehensive benefits.
Associate / Senior Associate, Competitive Intelligence and Strategy
Company: Entrada Therapeutics
Location: Boston, MA
Posted Oct 17, 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. You bring to the table the combination of an inquisitive spirit, critical thinking, and analytical 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. 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.
Dir/Sr Dir, HR Ops & Total Rewards
Company: Relay Therapeutics
Location: Cambridge
Posted Oct 16, 2023
Relay Therapeutics is seeking an experienced HR Operations leader to lead their dynamic People function. The role involves setting and overseeing the direction of the People Operations function, providing strategic input and operational leadership in compensation, benefits, and equity plans, mentoring and managing the People Operations team, building partnerships with key stakeholders, ensuring compliance with laws and regulations, and supporting the company's mission to bring life-changing therapies to patients.
Senior Product Manager
Company: Click Therapeutics
Location: New York City, NY
Posted Oct 15, 2023
Click Therapeutics is seeking a Senior Product Manager with experience in neuroscience, psychiatry, or digital health. The role involves collaborating with various experts to develop and deliver pipeline products through clinical trials and to market. The position is based in Tribeca, NYC, with a hybrid working model. The company offers competitive compensation, benefits, and a wealth-building opportunity at a fast-growing pre-IPO company.
Dir/Sr Dir, HR Ops & Total Rewards
Company: Relay Therapeutics
Location: Cambridge
Posted Oct 16, 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 teamBuild and foster partnerships with key stakeholders including Finance, Legal, Operations, IT, as well as external vendors and partnersEnsure that we have the key systems and processes in place to provide a seamless employee experience from onboarding to offboardingEnable 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 managementIn 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 organizationYou have a track record of developing strong partnerships with key stakeholders and other leadersYou 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 detailYou 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 presentingBiotech 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 HR Operations leader to lead this dynamic People function. This position provides leadership and strategic direction to the 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.
Senior Vice President, Clinical Development & Medical Affairs
Company: Click Therapeutics
Location: Miami, FL
Posted Oct 17, 2023
Click Therapeutics, a leading innovator in Digital Therapeutics, is seeking a Senior Vice President (SVP), Clinical Development & Medical Affairs. The role involves strategic leadership, clinical research and development, cross-functional collaboration, team management, regulatory oversight, and partnerships. The ideal candidate should have an MD/PhD background, extensive experience in CNS-focused biotechnology or pharmaceutical companies, and a strong understanding of CNS disorders and neuroscience. The position offers a competitive salary, performance-based bonuses, and a generous equity package, along with comprehensive benefits and a flexible work arrangement.
Senior Specialist/Manager, Regulatory Affairs
Company: Click Therapeutics
Location: New York City, NY
Posted Oct 16, 2023
Experience working with clinical trial design, terminology, and statistical concepts. 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. Qualifications: Bachelor's Degree required, preferred in life sciences, health care, or related discipline. 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. Manage processes involved with maintaining annual licenses, registrations, and listings. The final base salary will be dependent upon skills, experience and location. Familiarity with the legal basis of FDA's regulatory authority, including the US Food, Drug & Cosmetic Act and related amendments. All job postings will be listed on the Click Therapeutics official career page. Ability to form and maintain working professional relationships with external stakeholders (e.g., regulatory authorities, scientific and clinical advisors).
Senior Specialist/Manager, Regulatory Affairs
Company: Click Therapeutics
Location: New York City, NY
Posted Oct 16, 2023
Click Therapeutics is a company that develops and commercializes software as prescription medical treatments for people with unmet medical needs. They have a strong commitment to applying technical and scientific rigor and patient-centric design to their development process, resulting in clinically proven and FDA-regulated treatments. The company is looking for a Senior Specialist/Manager, Regulatory Affairs to drive the execution of regulatory initiatives for multiple Software as a Medical Device (SaMD) products.
Associate Director, Clinical Science
Company: Click Therapeutics
Location: Boston, MA
Posted Oct 15, 2023
Click Therapeutics is seeking an Associate Director of Clinical Science to lead the development and validation of digital therapeutics for serious diseases. The role involves managing clinical scientists, maintaining familiarity with scientific literature, and representing the team in collaborations. The ideal candidate should have a Ph.D. in Clinical Psychology or related field, strong understanding of adaptive behavior change, and at least two years of experience in digital health interventions. The position offers a competitive salary, annual performance-based bonus, and equity package. Click Therapeutics is committed to equal opportunity and offers a range of benefits including medical, dental, vision, life insurance, and more.