Jobs at Click Therapeutics
249,921 open positions
Senior Manager / Associate Director Biostatistics
Company: Corcept Therapeutics
Location: Peninsula
Posted Aug 28, 2023
Corcept Therapeutics, a company dedicated to cortisol modulation, is seeking a Senior Manager / Associate Director Biostatistics. The role involves leading statistical components of clinical trials, managing external statisticians, and ensuring regulatory compliance. The company values diverse perspectives and offers a competitive salary package, including bonuses and equity grants. The position can be hybrid (Bay Area) or remote (West Coast hours).
Clinical Trial Manager
Company: Click Therapeutics
Location: Miami, FL
Posted Aug 27, 2023
Click Therapeutics is a pre-IPO company in the fast-growing space of digital therapeutics, developing and commercializing software as prescription medical treatments for unmet medical needs. They have a groundbreaking clinical trial for their smoking cessation program and are progressing a pipeline of digital therapeutics for various high-burden therapeutic areas. The role of the Clinical Trial Manager (CTM) involves planning and executing traditional and decentralized clinical trials, managing operational aspects, and serving as the primary point of contact for study-related service providers, clients, and sites. The company offers great benefits, including stock options, competitive salary, 401(k) matching, performance-based cash bonus, comprehensive medical benefits, and more. They are committed to equal opportunity in employment and have a recruitment phishing scams warning.
Director, Program Management
Company: Entrada Therapeutics
Location: Boston, MA
Posted Aug 26, 2023
Entrada Therapeutics is a mission-driven organization focused on transforming the treatment of devastating diseases by developing a new class of medicines. Their Endosomal Escape Vehicle (EEV)-therapeutics enable efficient intracellular delivery of various therapeutics, improving the therapeutic index. The company is building a diverse pipeline of RNA-, antibody-, and enzyme-based programs for neuromuscular, immunological, ocular, and metabolic diseases. They are seeking a Director of Program Management to lead program team meetings, translate program goals into project tasks, and drive preclinical and clinical programs through key milestones. The ideal candidate will have a BS/BA degree, PMP certification, and 5+ years of experience managing cross-functional teams in drug development. Entrada offers competitive benefits, work-life balance, and a vibrant location in Boston's Seaport District.
Associate Scientist/Senior Associate Scientist
Company: Belharra Therapeutics
Location: San Diego, CA
Posted Aug 26, 2023
Belharra Therapeutics, an early-stage small molecule discovery company, is seeking a highly motivated biologist with a strong background in developing cell-based assays and experience in small molecule screening. The successful candidate will contribute to the growth of Belharra's research portfolio by selecting and screening high value targets in various cell-based assays. The role involves establishing and conducting cell-based assays, performing molecular biology techniques, tissue culture, and immune cell isolation. The ideal candidate should have a people-first approach, passion for problem-solving, strategic mindset, and a degree in Molecular and Cell Biology or related field with at least five years of industry experience. Belharra offers a collaborative, fun, and positive culture, commitment to talent and leadership development, competitive compensation, and excellent benefits.
Senior Specialist/Manager, Regulatory Affairs
Company: Click Therapeutics
Location: New York City, NY
Posted Aug 27, 2023
Click Therapeutics is a fast-growing pre-IPO company in the nascent and extremely exciting space of digital therapeutics. The company is committed to equal opportunity in employment and has a hybrid working model that consists of at least 3 days in office each week. The Senior Specialist, Regulatory Affairs role involves managing the drafting of high-quality regulatory submissions, coordinating collaborative input from cross-functional stakeholders, and providing regulatory direction when developing strategies for resolution. The role requires a Bachelor's Degree in life sciences, health care, or related discipline, 6-8 years of experience in an FDA regulated industry, and 3+ years of regulatory affairs experience. The company offers great benefits, including stock options, competitive salary with annual review, 5% 401(k) matching, annual performance-based cash bonus, comprehensive medical benefits, and industrious workspaces.
Senior Specialist/Manager, Regulatory Affairs
Company: Click Therapeutics
Location: New York City, NY
Posted Aug 27, 2023
Experience working with clinical trial design, terminology, and statistical concepts. 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. 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. Manage processes involved with maintaining annual licenses, registrations, and listings. 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. Familiarity with the legal basis of FDA's regulatory authority, including the US Food, Drug & Cosmetic Act and related amendments. Ability to form and maintain working professional relationships with external stakeholders (e.g., regulatory authorities, scientific and clinical advisors). Qualifications: Bachelor's Degree required, preferred in life sciences, health care, or related discipline.
Senior Specialist/Manager, Regulatory Affairs
Company: Click Therapeutics
Location: New York City, NY
Posted Aug 27, 2023
Click Therapeutics is a fast-growing pre-IPO company in the nascent and extremely exciting space of digital therapeutics. The company develops and commercializes software as prescription medical treatments for patients with unmet medical needs. They have a groundbreaking clinical trial for their smoking cessation program available nationwide and are progressing a broad pipeline of Digital Therapeutics for various high-burden therapeutic areas. The Senior Specialist, Regulatory Affairs role involves managing the drafting of high-quality regulatory submissions, coordinating regulatory strategy discussions, and providing regulatory intelligence. The company offers great benefits, including a competitive salary, stock options, comprehensive medical benefits, and unlimited vacation time.
Clinical Trial Manager
Company: Click Therapeutics
Location: Boston, MA
Posted Aug 27, 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. 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. 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. 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. 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. 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. Other than your email address or telephone number, which you may provide via a job application portal, Click Therapeutics will never ask you to provide personally identifiable information about yourself (such as a Social Security Number or Driver's License Number) via a messaging application (like that used on the LinkedIn platform or Microsoft Teams). WIRB, Advarra) Working knowledge of Good Clinical Practice (GCP) and US and international regulations for clinical trials Advanced written, oral, and interpersonal communication skills, including proficient knowledge of medical terminology Ability to deliver results and execute on required activities individually, in a team setting Organized and detail-oriented Strong negotiating skills in a compact clinical team working with aggressive timelines Ability to travel up to 20%, generally within the US Highly responsive and proactive, a team player Initiative, enthusiasm and a problem-solving approach to new challenges.
Senior Specialist/Manager, Regulatory Affairs
Company: Click Therapeutics
Location: New York City, NY
Posted Aug 27, 2023
Experience working with clinical trial design, terminology, and statistical concepts. Click Therapeutics will conduct interviews face-to-face over Zoom. Qualifications: Bachelor's Degree required, preferred in life sciences, health care, or related discipline. 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. Manage processes involved with maintaining annual licenses, registrations, and listings. 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. 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. Ability to form and maintain working professional relationships with external stakeholders (e.g., regulatory authorities, scientific and clinical advisors). All job postings will be listed on the Click Therapeutics official career page.
Head of Translational & Bioanalytical Sciences
Company: Spark Therapeutics, Inc.
Location: Philadelphia, PA
Posted Aug 28, 2023
Spark Therapeutics is seeking a Head of Translational & Bioanalytical Sciences to lead their cross-functional team. The role involves providing strategic and scientific leadership, ensuring appropriate translational, biomarker, and bioanalytical strategies are established and implemented. The individual will partner with Therapeutic Areas in Research and Clinical Development, serving as a bridge between Research & Development. Responsibilities include building a world-class organization, developing strategy for successful transition of drug discoveries into development programs, and defining translational & bioanalytical strategy from discovery through pre-clinical and clinical development.
Clinical Trial Manager
Company: Click Therapeutics
Location: Miami, FL
Posted Aug 27, 2023
Click Therapeutics is a fast-growing pre-IPO company in the nascent and extremely exciting space of digital therapeutics. They are progressing a broad pipeline of Digital Therapeutics across a variety of high-burden therapeutic areas, including MDD, Schizophrenia, Migraine, MS, Chronic Pain, Atopic Dermatitis, Acute Coronary Syndrome (ACS), Obesity, Oncology and more. The role of the Clinical Trial Manager (CTM) involves planning and executing traditional and decentralized clinical trials, managing all operational aspects for implementation of clinical trial activities, and serving as the primary point of contact. The CTM should have strong critical thinking skills for problem-solving and have strategic thinking capacity to drive study decisions that affect study outcomes and timelines. The role requires a Bachelor's Degree or Advanced Degree in life sciences, health care or related discipline, 2+ years as a Trial Manager in biotech, pharma, and/or CRO setting, and experience with commercial IRBs. The compensation includes a base salary range of $100,000 - $135,000, an annual performance-based cash bonus, and a generous equity package. The benefits include stock options, competitive Salary with Annual Review, 5% 401(k) matching, Annual Performance-Based Cash Bonus, Comprehensive Medical Benefits, Dental, Vision, Unlimited Vacation Time, Uber One, Nectar Rewards, One Medical, Fertility Support, Gym Pass, Citi Bike, Professional Development Stipend, Industrious Workspaces, Generous Paid Parental Leave, Commuter Subsidies, Monthly Lunch Stipend, Monthly Catered Lunches, Choice of Mac or Windows, Sponsored Company Events, Free, Unlimited Office Snacks and Beverages, and Much More...
Senior Director, Pipeline & Portfolio Market Planning
Company: Corcept Therapeutics
Location: Peninsula
Posted Aug 28, 2023
Advanced science degree preferred. MBA preferred.15+ years in drug/biotech industry7 - 10 years of relevant professional experience in roles such as new product planning, market planning, and/or portfolio managementExperience in a commercial leadership role that required comprehensive understanding of therapeutic markets from multiple customer perspectives (e.g., HCP, Payers, Patients) and/or different business perspectives (e.g., clinical, R&D, marketing)Leadership experience on drug development teams. Work directly with the product development team to influence clinical protocol development to ensure alignment with TPPs.Ensure early commercial strategies are developed, in partnership with Commercial Division leadership (e.g., early brand strategy, distribution strategy, patient advocacy engagement, scientific messaging, etc.). annual Board review, quarterly management review, integrated portfolio timeline, integrated portfolio revenue, etc.) Strong understanding of the drug development process for early through late-stage programsKnowledge of sales and marketingThe pay range that the Company reasonably expects to pay for this position is $242,600 - $285,400; the pay ultimately offered may vary based on legitimate considerations, including job-related knowledge, skills, experience, and education. Ability and experience in conducting market assessments of new opportunities. Solid understanding of market research principles.Ability to lead, influence, and gain consensus in a cross-functional team environment. 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 Lead these activities for early-stage programs and as-needed in partnership with DivisionsBusiness DevelopmentConduct asset assessments for business development opportunitiesLead initial Corcept deal team as part of BD diligence effortsPreferred Skills, Qualifications and Technical Proficiencies: Ability to master new therapeutic areas across multiple perspectives including clinical, commercial, and regulatory.Significant analytic skills with ability to clearly distill scientific, clinical, and commercial information into actionable insights. with regular reportingManage portfolio processes to facilitate Executive Team-level decision making, strategy, and budgeting. Capable of building strong rapport with development teamsFluent in the relationship between clinical trial design, label development, and promotional messaging.Strong management & leadership skills: ability to recruit talent and grow & lead a team of high performance individuals.Good communication skills; ability to develop and deliver compelling presentations to senior management and the Board of Directors.Understanding of industry code of conduct and ethicsPreferred Education and Experience: Bachelor's degree required. Drive portfolio process improvementsLiaison for Commercial functions on the Development Extended Leadership TeamPipeline Market PlanningDevelop data-driven insights and recommendations to support leadership in navigating complex, ambiguous business decisionsProvide physician, patient, and payer perspective into clinical strategy and planningDevelop & maintain long-range revenue forecasts and valuations for new programsConduct product opportunity assessments, including business development opportunitiesSynthesize data from various sources including primary market research, secondary data, and analytics into actionable insightsEvaluate ex-US pricing potential and commercial opportunity for pipeline productsNew Product PlanningProvide commercial leadership for development of pipeline programs and lifecycle extensions of on-market productsServe as a bridge between Commercial groups and Development.