Jobs at Click Therapeutics
249,921 open positions
Paralegal
Company: Corcept Therapeutics
Location: Peninsula
Posted Aug 13, 2023
Corcept is a commercial-stage company engaged in the discovery and development of drugs to treat severe endocrine, metabolic, oncologic and neurological disorders. The company has made significant revenue and net income in recent years. They have discovered a portfolio of over 1,000 proprietary selective cortisol modulators and are in various stages of clinical trials for different conditions. The company is also expanding its legal department and seeking a paralegal to support multiple areas of operations.
National Field Training Manager
Company: Corcept Therapeutics
Location: Peninsula
Posted Aug 12, 2023
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 The NFTM will also assist with the development & implementation of training initiatives for the Commercial organization, and the planning & execution of national and regional training meetings. Essential Responsibilities: Conduct regular field rides to ensure appropriate and effective execution and pull-through of training/marketing/sales initiativesAid the Director, Learning & Development, in the development of overall product training frameworks, programs, content, collateral, and rollout plans to increase sales force skills and knowledge with the goal of positively impacting sales resultsAssist in the execution of all Commercial training programs, including but not limited to new-hire onboarding, product training, industry updates, competitive landscape reviews, and sales skill development to ensure the maximum effectiveness of the sales forceFacilitate workshops and training classes on subjects including, but not limited to, those listed abovePartner with Sales Management, and Regional Training Liaisons (RTLs) to assess training gaps and work one-on-one in the field with our Clinical Specialists to address those gapsAssist in the planning and execution of National Field Meetings to align the Field Salesforce with current customer perspectives and Marketing brand goalsFacilitate ongoing distance learning programs in order to increase field competencies while minimizing time spent away from customersMaintain a high level of business intelligence, including new training methods, training programs and best practicesComply with all laws, regulations, and policies that govern the conduct of Corcept activitiesPreferred Skills & Qualifications:Proven track record of field sales successExcellent presentation and facilitation skillsExperience coaching and training field-based sales representatives is desiredStrong organizational skills with ability to manage multiple projects simultaneously and prioritize travel requirementsAbility to travel oftenPreferred Education and Experience:Bachelor's degree5+ years sales experience1+ years of field training experienceThe pay range that the Company reasonably expects to pay for this position is $165,500 - $180,000; the pay ultimately offered may vary based on legitimate considerations, including job-related knowledge, skills, experience, and education. In 2022, we generated revenue of $402 million and net income of $101 million.We have discovered a portfolio of more than 1,000 proprietary selective cortisol modulators. Our lead compounds are in Phase 2 and Phase 3 trials for the treatment of patients with Cushing’s syndrome, advanced ovarian cancer, castration-resistant prostate cancer and amyotrophic lateral sclerosis (“ALS”). We plan to initiate a Phase 2b trial in patients with non-alcoholic steatohepatitis (“NASH”) by the end of this year. Every year, we advance new molecules to the clinic.Over the next few years, we expect to submit several new drug applications.National Field Training ManagerThe National Field Training Manager will provide initial disease state and product training for newly hired Clinical Specialists (CSs), as well as ongoing field training for the Salesforce with a strong focus on observing CS activities via field rides. This will include the deployment of training curriculum for the rollout of new Marketing & clinical education materials and product updates. Since 2012, we have marketed Korlym® for the treatment of patients suffering from Cushing’s syndrome, a life-threatening orphan disorder caused by excess cortisol activity. Corcept is a commercial-stage company engaged in the discovery and development of drugs to treat severe endocrine, metabolic, oncologic and neurological disorders by modulating the effects of the hormone cortisol.
Research Associate II, Biology (Neuroscience)
Company: Voyager Therapeutics
Location: Cambridge
Posted Aug 14, 2023
Voyager Therapeutics is a biotechnology company dedicated to gene therapy and neurology. They are seeking an experienced biologist to contribute to their research team in Cambridge, Massachusetts.
Sr. Manager, GMP Compliance
Company: CymaBay Therapeutics
Location: North Jersey
Posted Aug 11, 2023
4, as well as other international regulations scientific and business professionals who are highly motivated, collaborative.Excellent interpersonal skills, including listening, writing, negotiating positions, facilitating discussions, possess great attention to detail.Manages competing demands; Changes approach or method to best fit the situation; Able to deal with frequent change, delays, or unexpected events.Follows instructions and responds to management direction; Takes responsibility for own actions.Demonstrates accuracy and thoroughness; Looks for ways to improve and promote quality; Applies feedback to improve performance; Monitors own work to ensure quality.Identifies and resolves problems in a timely manner; Gathers and analyzes information skillfully.Communicates changes and progress; Completes tasks on time or notifies appropriate person with an alternate plan.Excellent computer proficiency (MS Word, Excel, PowerPoint)Ability to travel up to 20-30% domesticallyEDUCATION, CERTIFICATES, LICENSES, REGISTRATIONSBachelor of Science degreeCertified Quality Auditor is desirableThe anticipated salary range in Newark, California is $170,000 - $185,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. CymaBay is a multi-state employer, and this salary range may not reflect positions that work outside of the Bay Area or in other states. This is a hands-on role reporting to the VP of Quality.ESSENTIAL DUTIES AND RESPONSIBILITIESResponsible for planning managing and conducting internal and external GMP audits of CMOs/CDMOs per defined timelines.Acts as a central point of control for the resolution of internal and external audit findings while ensuring audit reports are issued and debriefs conducted in a timely manner.Work collaboratively with commitment owners to ensure that all commitment timelines are met via proactive CAPA tracking, and confirm their timely closure and ensure suitable effectiveness checks are implemented.Collaborates with management to identify, evaluate, and recommend solutions to issues identified during performance of GMP audits.Develops and provides meaningful metrics and trends to Management.Ability to apply principles of logical and scientific thinking to a wide range of technical and practical small molecule manufacturing applications.Lead proactive evaluation and education of site GMP compliance against current and emerging regulatory trends.Supports regulatory inspections in the creation, maintenance and management of inspection content, ensuring it is organized, current and readily accessible at all times.Evaluate and manage proposed commitments to regulatory authorities/audit bodies in response to inspection/audit findings.Complete other responsibilities, as assigned.MINIMUM QUALIFICATIONSRequires 6+ years of relevant experience, preferably in the pharmaceutical or biotech industries or related field or equivalent.Working Knowledge and experience with 21CFR210 & 211, ICHQ7, 21CFR600,21CFR11, Eudralex Vol. As part of the inspection readiness program, the Senior Manager evaluates external guidance and regulations, ensures visibility and awareness of emerging new or changing standards. Manager, GMP Compliance will be responsible for conducting internal and CMO/CDMO audits, assisting in inspection/audit preparation activities, and supporting GMP regulatory inspections for CymaBay Therapeutic Inc.’s (CymaBay) clinical and commercial programs. The Senior Manager works with internal functional groups and CMO/CDMOs to support global activities and provides cGMP compliance audit trends and metrics to Management. POSITION SUMMARYThe Sr.
Director, Commercial Strategy
Company: Click Therapeutics
Location: New York City, NY
Posted Aug 10, 2023
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. Click Therapeutics will conduct interviews face-to-face over Zoom. 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. Competitive Salary with Annual Review | Annual Performance-Based Cash Bonus | Stock options | 5% 401(k) matching | Comprehensive Medical Benefits | Dental | Vision | Voluntary Benefits | Unlimited PTO | Uber One | Nectar Rewards | One Medical | Fertility Support | Gym Pass | Citi Bike | Professional Development Stipend | Weekly Grubhub Lunches | Generous Paid Parental Leave | Industrious Workspaces | Commuter Subsidies | Choice of Mac or Windows | Sponsored Company Events | Office Snacks and Beverages | Much More...Equal Employment OpportunityClick 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. If you have any questions regarding the validity of a recruitment inquiry or an interview, please contact the Click's recruitment team at [email protected] to confirm before proceeding. as they relate to partnership deals Sharing cross-learnings of processes and activities between our pharma partners and our internal program Qualifications: Bachelor's degree required (MBA or other advanced degree preferred) 10-15 years of experience in pharmaceutical/biotech (Commercial strategy, franchise or brand global teams, sales, market access, pricing, marketing), project management, corporate communications, or a related field 7-10 years experience managing and executing on relationships with internal (cross-matrix teams) and/or external partners (consulting clients, co-promote partnerships, etc.) All job postings will be listed on the Click Therapeutics official career page. Click Therapeutics may at its business discretion decide to or refrain from obtaining, maintaining and/or extending the temporary visa status and/or sponsoring a colleague for permanent residency and /or employment eligibility, considering factors such as availability of qualified U.S. workers and the colleague's long-term prospects for securing lawful permanent residence, among other reasons. Strong leadership experience in Commercial Strategy such as Market Access, Commercialization, and Launch Management (US and & ex-US preferred) Prior pharmaceutical product launch experience Prior experience working with pipeline assets in phase III or earlier Extensive experience or knowledge of the US prescription markets such as market landscapes, value assessments, regulatory environments and requisite timelines Demonstrated understanding of cross functional commercial areas, including sales, marketing analytics, payer, pricing, and sales training Proven ability to conceive, develop and implement business plans for products in various markets Ability to analyze complex data and information and develop key strategies and solutions to address issues Excellent interpersonal skills with the ability to lead, interact with, focus, resolve conflict and drive consensus among individuals from a variety of cultures, and disciplines Ability to travel within and outside of the US as needed Preferred Qualifications: Knowledge of, or experience with, Digital Therapeutics and/or Prescription Digital Therapeutics is considered a plus Expertise in at least one of the following commercial functions: Marketing, Field Sales, Sales Enablement, Commercial Excellence, Pricing & Contracting Compensation:The base salary range for this position is between: $225,000 - $250,000. The final base salary will be dependent upon skills, experience and location.
Senior Product Manager
Company: Force Therapeutics
Location: Remote
Posted Aug 10, 2023
Monitor product adoption and gather feedback for continuous improvement.Other related duties as requiredWhat we’re looking for:5+ years of Product Management experience, preferably in a B2B SaaSDemonstrated success with shipping client facing features and applicationsData-driven with a the ability to measure the impact of new featuresExperience with continuous discoveryDemonstrated success with crafting product requirements, specifications and user storiesStrong technical understanding and experience using product analytics tools (Pendo a plus)Team player, self-directed, keen listener, excellent communicator, strong presentation skillsCompensation and Benefits: Salary range between $135,000 - $145,000 based on experience and locationMedical, Dental, Vision Insurance401k retirement planningPre-tax commuter benefitsUnlimited sick and safe leaveGenerous PTORemote friendly workplace You will be an expert at bridging the communication gap between business and technology and help translate the “What” into the “How”. This is a highly collaborative role, working with another product manager, our product designer, and other Force teams to manage short and longer-term product roadmaps to meet business needs, create investment rationale, and prioritize projects and features within projects.Key Responsibilities:Partner cross-functionally to listen, learn and act on findings to help shape the roadmap and overall product strategyLeverage qualitative and quantitative learnings to deeply understand our users and prioritize new initiativesMeasure the success of product features after release and optimize their performance through rapid, data-driven and client informed iterationCommunicate with internal stakeholders on new and upcoming features and the outcomes of previous launchesBe curious and stay up-to-date on competitors and industry standards by performing market assessments and incorporating best practices into our agile workflowsConduct market research, competitive analysis, and user research to identify market trends, customer preferences, and opportunities for product innovation.Work with designers and UX specialists to create intuitive and user-friendly product experiences, ensuring usability and accessibility for the target user base.Implement agile methodologies to drive product development, including sprint planning, backlog management, and facilitating effective communication and collaboration within the team.Coordinate and support product launches, including go-to-market strategies, pricing, positioning, and communication plans. The Product Team closely collaborates across the organization, with Engineering, Client Success & Strategy, and our Marketing Team, to deliver an innovative product that is consistently at the forefront of digital patient engagement.About the role:We are looking for a Senior Product Manager to join our team -- you’ll be providing vision and direction to ensure we develop innovative solutions that provide maximum business value through an outstanding user experience You will help align folks around common objectives by understanding each team’s viewpoint and company goals. The clinical and financial impacts of Force have been validated across 145 studies with surgeon leaders. We are a dynamic group, passionate about our Company’s mission and the use of digital care to solve big health care problems.About the Product TeamOur agile and highly collaborative Product Team at Force drives product ideation process all the way through to feature development and releases. The business has a variety of clients which include Academic Medical Centers, ASC and large PE back practices. About Force TherapeuticsForce Therapeutics is a leader in digital care providing a SaaS based platform used by over 700,000 patients to recover from surgery at hundreds of facilities nationwide.
Associate Director of Procurement
Company: Dragonfly Therapeutics
Location: Waltham
Posted Aug 15, 2023
Dragonfly Therapeutics is seeking an Associate Director of Procurement to develop and lead procurement strategies. The successful candidate will play a critical role in developing an inter-department procurement strategy and managing contracts with external vendors.
Scientist/Senior Scientist, Bioanalytical Sciences
Company: Voyager Therapeutics
Location: Cambridge
Posted Aug 13, 2023
Voyager Therapeutics is a biotechnology company dedicated to breaking through barriers in gene therapy and neurology. The company is leveraging cutting-edge expertise in capsid discovery and deep neuropharmacology capabilities to address delivery challenges. Voyager's TRACER AAV capsid discovery platform has generated novel capsids with high target delivery and blood-brain barrier penetration. The company is in partnership with several pharmaceutical giants and has multiple programs in its pipeline, including preclinical programs in Alzheimer's disease, amyotrophic lateral sclerosis (ALS), Parkinson's disease, and other central nervous system diseases. Voyager is seeking an experienced Scientist / Senior Scientist to join its Bioanalytical Sciences team in Cambridge, Massachusetts.
Research Associate – Analytical Testing Support
Company: Shape Therapeutics
Location: Seattle, WA
Posted Aug 12, 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 this role is $61,000-$83,000. Additional compensation may include annual target bonus and/or sign-on bonus, equity grant and relocation bonus. The hired applicant's placement within the range is based on qualifications and professional experience. The ideal applicant will have experience analyzing DNA, RNA, or protein modalities. 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. qPCR, ddPCR, immunoassays, HPLC, Flow cytometry)Keep organized and detailed records using an electronic laboratory notebookMaintain laboratory supplies reagent inventoryPerform other tasks and duties as assigned by P&PD or ShapeTX managementWhat you Bring:Qualifications:Bachelor of Science degree in Biochemistry, Biology, Chemistry, or related discipline1-2 years of industry experience preferredSkills and Experience:Hands-on experience in protein or virus analysisqPCR/ddPCR principles and analysisELISA and other ImmunoassaysFamiliarity with common data analysis software (eg Excel, GraphPad Prism, JMP)Ability to troubleshoot and think analyticallyStrong work ethic and attention to detailAbility to multitask and support multiple projects simultaneouslyAbility to work collaboratively in a team-science environmentAbility to think creatively and tackle challenges with a problem-solving attitudeExcellent written and verbal communication skillsPreferred Qualifications:Experience operating HPLC instrumentsExperience performing NGS library preparationCompensation & Benefits ShapeTX offers a robust benefits package, including but not limited to: Medical, Dental and Vision coverage for employees and their eligible dependents. Detail oriented, a collaborative spirit and a desire to work in a fast-paced startup environment are essential.What You’ll Do:Perform qPCR, ddPCR, and/or ELISA assays to support P&PD experimentsIndependently follow established protocols, analyze and communicate resultsPerform a broad range of relevant analytical techniques to help quantify and characterize AAV (e.g. 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.We are seeking a Research Associate, Analytical Testing Support.
Translational Bioinformatician (Director/Senior Director)
Company: Dragonfly Therapeutics
Location: Waltham
Posted Aug 13, 2023
Dragonfly Therapeutics is seeking a highly skilled Director/Senior Director, Translational Bioinformatics to work closely with Translational Medicine and Clinical Development teams. The role involves leveraging expertise in computational biology/genomics to analyze clinical/translational datasets, define target populations, and discover predictive biomarkers. The successful candidate will need to have a PhD in Bioinformatics, Computational/Systems Biology, Biostatistics, or a related field, at least 5 years of experience in industry drug discovery and development, and strong proficiency in programming languages such as Python and R.
Research Associate/Sr. Research Associate (Pipeline Research)
Company: Shape Therapeutics
Location: Seattle, WA
Posted Aug 09, 2023
DNA isolation, RNA isolation, cDNA generation, qPCR, ddPCR, immunoblotting, immunofluorescence staining, imaging etc. Employees are eligible to enroll in our Company’s voluntary 401k plan, voluntary Life/AD&D and Voluntary FSA’s.The salary range for the Research Associate role is $61,000-$83,000, and the salary range for the Senior Research Associate is $72,000-$98,000. 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! )Occasionally assist in animal maintenance, surgery, blood collection, injections, tissue harvests (< 10% of time)Maintain a detailed electronic laboratory notebookWhat You Bring:Preferred Qualifications:BS/MS degree in Neuroscience, Molecular/Cellular Biology or related discipline1-3 years of experience post-degree in an academic or industry laboratory settingAbility to work both independently and collaborativelySkills and Experience:Mammalian cell culture and good aseptic techniqueExperience culturing primary mouse neurons and iPSC cell lines preferredStrong background in molecular work such as DNA/ RNA purification, cDNA synthesisqRT-PCR/ddPCR principles and analysisFlow cytometry/ cell sortingWestern blot / ELISAImmunostaining and fluorescence microscopyRodent handling and a desire to learn more complex skills preferredAbility to troubleshoot and think analyticallyStrong work ethicA collaborative, team playerAttention to detailEffective communicationAbility to multitask and support multiple projects simultaneouslyShapeTX offers a robust benefits package, including but not limited to: Medical, Dental and Vision coverage for employees and their eligible dependents. This is an excellent opportunity to join the Pipeline Research team and advance the next generation of transformative gene therapies towards the clinic.What You’ll Do:Under supervision, design and execute rigorous and well-controlled experimentsFollow established protocols, analyze data, and communicate results with supervisorAssist in tissue culture: cell line maintenance, generation of primary neuronal culturesPerform a broad range of cell/molecular biology techniques (e.g. Neuroscience experience is a plus. The hired applicant's placement within the range is based on qualifications and professional experience. An ideal candidate will have general cellular and molecular biology experience, a teachable and collaborative spirit, and a desire to work in a fast-paced start-up environment.
Manager, Drug Safety & Pharmacovigilance
Company: Corcept Therapeutics
Location: Peninsula
Posted Aug 09, 2023
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 In this role, the individual will be primarily responsible for ensuring end to end safety reporting requirements and processes are established and maintained for clinical trials (phase 1-4). This role will also support post marketing safety operation activities, as needed.Core Responsibilities: Support the oversight of drug safety/pharmacovigilance service providers to ensure collection, processing, reporting and reconciliation of adverse events reports is compliant with global regulatory requirements and standard operating procedures (SOPs)Serves as a Safety Operations Lead on study management team(s).Create/revise and implement department SOPs, work instructions, and Safety Management Plans (SMPs).Develop and deliver training for safety related topics for internal personnel and external vendors.Perform in line and/or end of line quality review of adverse event reports.Support process improvement initiatives and safety systems implementation/maintenance activities.Ensure the clinical trial master file (TMF) is maintained in an inspection ready state for all safety related documents.Support and participate in audits and inspections, including preparation activities.Assist with safety operations and/or safety science projects, as necessary.Required Skills, Qualifications and Technical Proficiencies:Knowledge of Argus (or similar safety applications), electronic data capture systems, and MedDRA and WHO Drug coding dictionaries.Excellent communication and collaboration skills in a multidisciplinary team.Ability to work independently and manage multiple projects in a dynamic, fast-paced environment to meet patient and corporate needs.Able to occasionally work extended and/or flexible schedule to meet corporate needs. Education and Experience: Bachelor's degree in healthcare or life sciences- degree such as RN or BSN, PharmD is preferred.Minimum of 5 years Drug Safety/PV experience in a global environmentExperience in both clinical and post marketing safety operations preferred.Working knowledge of FDA, EU and ICH guidelines for safety reporting and processing for clinical trials and post marketingThe pay range that the Company reasonably expects to pay for this position is $147,000 - $173,000; the pay ultimately offered may vary based on legitimate considerations, including job-related knowledge, skills, experience, and education. In 2022, we generated revenue of $402 million and net income of $101 million.We have discovered a portfolio of more than 1,000 proprietary selective cortisol modulators. Our lead compounds are in Phase 2 and Phase 3 trials for the treatment of patients with Cushing’s syndrome, advanced ovarian cancer, castration-resistant prostate cancer and amyotrophic lateral sclerosis (“ALS”). We plan to initiate a Phase 2b trial in patients with non-alcoholic steatohepatitis (“NASH”) by the end of this year. Every year, we advance new molecules to the clinic.Over the next few years, we expect to submit several new drug applications.This position supports drug safety and pharmacovigilance operation activities in both clinical trials and post marketing settings. Since 2012, we have marketed Korlym® for the treatment of patients suffering from Cushing’s syndrome, a life-threatening orphan disorder caused by excess cortisol activity. Corcept is a commercial-stage company engaged in the discovery and development of drugs to treat severe endocrine, metabolic, oncologic and neurological disorders by modulating the effects of the hormone cortisol.