Jobs at Click Therapeutics
249,921 open positions
DMPK Director
Company: Genesis Therapeutics
Location: San Diego, CA
Posted Dec 30, 2024
Genesis Therapeutics is seeking a motivated and experienced DMPK Director to lead drug metabolism and pharmacokinetics studies for their small molecule drug discovery and early development pipeline. The successful candidate will provide leadership in designing, analyzing, and reporting in vitro and in vivo DMPK/ADMET studies, and participate in data integration for AI ADME predictive models. The role offers full medical and dental benefits, flexible work hours, and vacation. Genesis Therapeutics is a biotech startup with a focus on unifying AI and biotech to discover novel treatments for severe and devastating conditions.
Senior Principal Process Improvement Consultant
Company: Prime Therapeutics
Location: Other US Location
Posted Dec 30, 2024
The text describes a job posting for a Senior Principal Process Improvement Consultant at Prime Therapeutics. The role involves partnering with subject matter experts and executive leadership to deliver innovative solutions, leading strategic initiatives, and collaborating with enterprise partners. The candidate should have a Bachelor's degree in Business or Healthcare Administration, 10 years of related work experience, and strong communication skills. The position offers a competitive salary and benefits package.
Associate Director, CMC Biologics
Company: Dyne Therapeutics
Location: Waltham
Posted Dec 30, 2024
Dyne Therapeutics is a clinical-stage muscle disease company focused on advancing innovative life-transforming therapeutics for people living with genetically driven diseases. They have 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). The Associate Director CMC Biologics is responsible for supporting internal CMC capabilities and managing external CDMOs under cGMP.
Senior Manager/Associate Director, PV Scientist
Company: Dragonfly Therapeutics
Location: Waltham
Posted Dec 29, 2024
Dragonfly Therapeutics is seeking a Senior Manager/Associate Director with a strong background in Drug Safety Specialist to join their team. The role involves monitoring and assessing the safety of their products, ensuring compliance with global pharmacovigilance regulations, and contributing to safety operations activities with vendors and partners. The successful candidate will work closely with cross-functional teams to ensure accurate reporting and management of safety information, and contribute to the preparation of DSURs, aggregate reports, and other regulatory documents.
Senior / Staff Product Manager - Science & Technology
Company: Genesis Therapeutics
Location: Peninsula
Posted Jan 16, 2025
Genesis Therapeutics is hiring a Senior Product Manager to lead the development of their innovative drug discovery platform, Nucleus, and computational methods research platform. The role involves defining and communicating the product roadmap, collaborating with multidisciplinary teams, driving project execution, and engaging with stakeholders. The ideal candidate should have 5+ years of product management experience in a technical or scientific environment, strong communication skills, and familiarity with agile development practices. Experience in the pharmaceutical, biotech, or technology sectors is highly desirable.
Payer Account Management & Trade Lead
Company: Intellia Therapeutics
Location: Cambridge
Posted Dec 31, 2024
Intellia is seeking an experienced Payer Account Management and Trade Sr Dir to lead efforts in building capabilities for the upcoming launch of a groundbreaking gene-editing therapy. The role involves establishing payer partnerships, creating a robust distribution strategy, and optimizing access channels to ensure the therapy reaches patients in need. The successful candidate will be responsible for developing and executing an integrated account management and trade strategy to support the successful launch of the gene-editing therapy.
Specialist, Office Operations
Company: Tango Therapeutics
Location: Boston, MA
Posted Jan 16, 2025
Tango Therapeutics, a biotechnology company in Boston, Massachusetts, is seeking a receptionist with 13 years of administrative assistant experience. The role involves greeting visitors, managing calls, ordering lunches, maintaining office supplies, and providing general office support. The ideal candidate should be proficient in Microsoft Office, have excellent organizational skills, and possess a welcoming and hospitable approach. The company values diversity and equal opportunity.
Regional Account Manager
Company: Mahana Therapeutics
Location: Remote
Posted Dec 28, 2024
Mahana is seeking driven sales professionals to join their team and drive demand and market growth with target audiologists and hearing loss clinics. The ideal candidate must have experience in the hearing healthcare market, be motivated, and have a proven ability to succeed in closing and driving rapid sales growth. The position requires excellent communication skills, the ability to work in a fast-paced environment, and a passion for improving the lives of millions of tinnitus sufferers.
Senior Director, Pharmacovigilance
Company: BlueRock Therapeutics
Location: Cambridge
Posted Jan 15, 2025
The Senior Director Pharmacovigilance will report to the Vice President Head of Global Safety and Pharmacovigilance, responsible for supporting the Development organization as a PV expert. Key responsibilities include serving as safety lead for assigned products, providing independent oversight of daily safety monitoring activities, leading the signal management process, and providing PV subject matter expertise on crossfunctional teams. The role requires a degree in Pharmacy, Nursing, Epidemiology, Biosciences, or equivalent healthcare degree with pharmaceutical industry background and proven competence in PV. Minimum of 8 years pharmaceutical industry experience, including 5 years in PV, is required. Knowledge of MedDRA terminology, experience reviewing cumulative safety data, and understanding of the drug development process are essential. Excellent communication skills and ability to work effectively in a collaborative team environment are also required.
Trial Master File (TMF) Senior Specialist
Company: Apogee Therapeutics
Location: Remote
Posted Jan 07, 2025
Apogee Therapeutics, a Nasdaq-listed biotech company founded in 2022, is seeking a Trial Master File (TMF) Senior Specialist. The role involves managing TMF records, ensuring studies are inspection-ready, and adhering to ICH-GCP guidelines. The ideal candidate should have a BA/BS in a science/healthcare field, 3-5 years of relevant clinical operations experience, and proficiency in MS Office Suite. The company offers a competitive salary, benefits, flexible PTO, and opportunities for professional growth.
Executive Assistant & Human Resources Operations
Company: Lycia Therapeutics
Location: Peninsula
Posted Dec 30, 2024
Lycia Therapeutics Inc is a biotechnology company using its LYTAC platform to develop first-in-class therapeutics. They have raised significant capital and are advancing an internal pipeline of novel degraders. In May 2024, they completed a $1066 million series C financing. The company is seeking an Executive Assistant for HR Operations.
TMF (Trial Master File) Manager
Company: Apogee Therapeutics
Location: Remote
Posted Jan 07, 2025
Apogee Therapeutics, a Nasdaq-listed biotech company founded in 2022, is seeking a Trial Master File (TMF) Manager. The role involves day-to-day management and oversight of the TMF for respective studies, acting as the main point of contact and TMF Subject Matter Expert. Key responsibilities include ensuring TMF quality, compliance, and inspection readiness, providing guidance to the study team and CRO, and developing successful working relationships with TMF stakeholders. The ideal candidate should have an ABS degree in a science/healthcare field, 8-10 years of relevant clinical operations experience, and 7+ years of TMF management experience. Proficiency in Microsoft Office and understanding of the clinical trial lifecycle are required. The company offers a competitive compensation package, professional growth opportunities, and a culture grounded in its CORE values.