Jobs at Click Therapeutics
Click Therapeutics is a Boston-based digital therapeutics company that delivers prescription digital therapeutics for opioid use disorder and other substance use disorders. Their flagship product, Click, combines evidence‑based CBT and motivational interviewing with AI‑driven personalization, earning FDA clearance and partnering with leading pharma companies to scale impact.
Roles span software engineering, data science, product management, clinical research, regulatory affairs, quality assurance, and business development. Candidates can expect agile, cross‑functional teams focused on behavioral health outcomes, remote‑first or hybrid work options, and a culture that rewards measurable impact in patient care.
Job Transparency gives candidates direct access to Click Therapeutics’ salary ranges, employee sentiment, and interview insights, empowering you to benchmark offers, negotiate effectively, and gauge fit before you apply.
Senior Director, Targeted Sciences
Company: Bicycle Therapeutics
Location: Cambridge
Posted Jan 30, 2025
Bicycle Therapeutics, a clinical-stage biopharmaceutical company, is seeking a Target Science Lead Senior Director with a strong oncology background. The role involves leading the discovery and validation of high-value targets to expand the company's BTC and BRC pipelines. The ideal candidate will have extensive experience in oncology drug discovery, a deep understanding of cancer biology, and a proven track record of identifying and validating therapeutic targets. The role is hybrid, requiring at least 3 days onsite per week. The company offers a competitive reward package, flexible working environment, and commitment to building a diverse workforce.
Specialist III Bioinformatics
Company: BlueRock Therapeutics
Location: New York City, NY
Posted Jan 30, 2025
BlueRock Therapeutics is looking for a skilled bioinformatics professional to join their team in New York. The ideal candidate should have a PhD or MS in bioinformatics, computational biology, biomedical engineering, or a related field, with at least 2 years of experience. Alternatively, a BS with at least 4 years of experience is acceptable. The role involves developing internal scientific software, building and analyzing NGS pipelines, and assisting in software deployment and knowledge transfer. The candidate must be proficient in Python, R, and Bash, and have a strong understanding of molecular and cellular biology. Effective communication and time management skills are also required. This is a unique opportunity to contribute to the development of cellular therapies using BlueRock's unique CELL+GENE platform.
Head of Platform Engineering
Company: Genesis Therapeutics
Location: Peninsula
Posted Jan 28, 2025
Genesis Therapeutics is a leading biotech company that combines AI and biotech to discover novel treatments for severe diseases. The company's platform, GEMS, is the industry's most advanced molecular AI platform for small molecule drug discovery. Genesis has a strong team of biotech leaders, drug hunters, deep learning researchers, and software engineers. They have raised over $300M in funding and have collaborations with major pharmaceutical companies. The Head of Platform Engineering will lead the development and maturation of the platform, driving innovation and ensuring high-quality, scalable solutions for drug discovery.
Senior Supply Chain Coordinator (Contract)
Company: Kyverna Therapeutics
Location: Other US Location
Posted Jan 28, 2025
Kyverna Therapeutics is hiring a Senior Supply Chain Coordinator Contractor for a hybrid role based in Emeryville, CA. The role involves supporting the Manufacturing team, managing logistics for temperature-sensitive materials, coordinating order management processes, and collaborating with various teams. The ideal candidate should have an Associate's or Bachelor's degree, experience in supply chain, manufacturing, global trade compliance, clinical trial logistics, or cell and gene therapy. Kyverna is an Equal Opportunity Employer.
Sr. Analyst, Quality Control
Company: Abeona Therapeutics
Location: Cleveland, OH
Posted Jan 30, 2025
The Quality Control Senior Analyst I position involves driving routine laboratory activities in support of Good Manufacturing Practices (GMP) testing. The role includes conducting training, serving as a backup analyst for Environmental Monitoring, authoring and revising analytical methods, reviewing documentation, participating in validation, driving process improvements, and maintaining laboratory compliance. The ideal candidate should have a BS in biochemistry, biology, microbiology, molecular biology, or a related field with 5-7 years of relevant experience in the pharmaceutical or biotech industry. Good mathematical and organizational skills, as well as the ability to interact constructively with coworkers, are required.
Quality Control, System Administrator
Company: Abeona Therapeutics
Location: Cleveland, OH
Posted Jan 30, 2025
The Quality Control System Administrator role involves ensuring the implementation and rollout of third-party business applications, such as Laboratory Information Management Systems (LIMS). The position requires technical expertise in analyzing, designing, developing, testing, implementing, supporting, and documenting complex business applications. The administrator will be responsible for maintaining and managing installs, upgrades, patches, and troubleshooting of third-party packaged business applications. They will also handle support tickets, collaborate with software developers, and perform other duties as assigned. The ideal candidate should have a BS in Biochemistry, Biology, Microbiology, Molecular Biology, Computer Science, or a relevant discipline, with 2-4 years of related LIMS experience. Familiarity with IT systems in a Laboratory environment and proficiency in the Windows environment are required. Some weekend work or late nights may be required periodically.
Manager/Senior Manager - Supplier Quality Management
Company: Allogene Therapeutics
Location: USA
Posted Jan 30, 2025
Allogene Therapeutics, a clinical-stage biotech company in South San Francisco, is developing allogeneic CAR T cell products for cancer and autoimmune diseases. They seek a highly motivated individual with 10+ years of quality assurance experience for a role in their Supplier Qualification Management program, focusing on quality agreement negotiation and management. The ideal candidate will have extensive knowledge of quality system requirements, excellent communication skills, and the ability to work in a fast-paced environment. Proficiency in MS Office and Veeva is required, with US work authorization needed.
Quality Control Analyst I (QC Analytical)
Company: Abeona Therapeutics
Location: Cleveland, OH
Posted Jan 30, 2025
The Quality Control Analyst I position involves performing routine laboratory activities in support of Good Manufacturing Practices (GMP) testing for Quality Control (QC). The role includes tasks such as qPCR, immunostaining, protein characterization, and product-specific analytical test methods. The analyst will interact with employees both internally and externally to Quality Control. Essential duties include training on SOPs and methods, performing in-process and finished drug product analysis, maintaining organized laboratory records, and contributing to improving QC systems and procedures. The ideal candidate should have a BS in a relevant discipline with 1-3 years of experience, preferably in the pharmaceutical or biotech industry within a GMP or GLP environment. Experience in cell culture, qPCR, and protein analysis is preferred. Good mathematical and organizational skills, along with the ability to interact constructively with coworkers, are required. Some weekend work or late nights may be necessary periodically.
Associate Director, HR Business Partner
Company: Bicycle Therapeutics
Location: Cambridge
Posted Jan 29, 2025
Bicycle Therapeutics is a clinical-stage pharmaceutical company based in Cambridge, UK and Cambridge, MA, USA. They are developing a novel class of medicines called Bicycle® molecules for diseases underserved by existing therapeutics. The company is currently evaluating several candidates in company-sponsored clinical trials. The role in question is a global HR Business Partner position, responsible for driving performance, building engagement, and supporting locationspecific matters. The ideal candidate should have a progressive HR agenda, strong consulting and coaching skills, and a deep understanding of employment legislation. The company offers a flexible working environment, competitive rewards, and a commitment to diversity and inclusion.
Influencer Marketing Lead
Company: Pendulum Therapeutics
Location: San Francisco, CA
Posted Jan 31, 2025
Pendulum is a company revolutionizing health and wellness by focusing on the human microbiome. They have developed proprietary probiotic pipelines and a unique discovery platform to identify key bacterial strains and prebiotics. Their medical probiotics have transformed the consumer probiotics market into a new category of therapeutic offerings. Pendulum is seeking a strategic and results-driven Influencer Marketing Lead to build their influencer program from the ground up, focusing on driving revenue through performance-based partnerships with healthcare professionals, medical experts, and wellness authorities.
ML Infrastructure Engineer (Senior / Staff / Principal)
Company: Genesis Therapeutics
Location: Peninsula
Posted Jan 31, 2025
Genesis Therapeutics is a leading AI-driven biotech company focused on small molecule drug discovery. They are seeking experienced ML engineers to lead engineering efforts for generative modeling of molecular systems. The role involves leading rapid iteration on the AI platform, optimizing GPU operations, and defining the long-term vision for the ML platform. The company offers competitive compensation, comprehensive benefits, and a collaborative work environment.
Manager/Senior Manager, Supplier Quality Management (Contract)
Company: Allogene Therapeutics
Location: Peninsula
Posted Jan 30, 2025
Allogene Therapeutics, a clinical-stage biotech company in South San Francisco, is seeking a quality-focused professional for a new role in their Supplier Qualification Management (SQM) program. The ideal candidate will have extensive experience in quality assurance, quality agreement negotiation, and management, with a strong understanding of US FDA GMP, GCP, EMA, and ICH guidelines. They should possess excellent communication skills, be comfortable in a fast-paced environment, and have proficiency in MS Office. Veeva experience is a plus. Allogene offers a collaborative work environment and competitive pay based on experience, qualifications, and business needs.