Nuvalent, Inc. is a biotechnology company focused on developing precisely targeted therapies for cancer patients. Utilizing structure-based design, Nuvalent creates innovative small molecules with high target selectivity to overcome resistance and minimize adverse events. The company advances a pipeline of lead programs targeting ROS1-positive and ALK-positive NSCLC, along with multiple discovery-stage research initiatives.
Open Positions
Associate Director, Supply Chain Logistics & Compliance
10+ years of experience in logistics within the biotech/pharmaceutical industry, Bachelor’s degree in business administration, Operations Management, Engineering or similar
Senior Manager, Regulatory Affairs
6-8 years of experience in Regulatory Affairs, Bachelor or advanced degree in a scientific field or equivalent work experience
Associate Director, Drug Safety and Pharmacovigilance Scientist
4+ years' experience in Drug Safety / Pharmacovigilance, degree in a medical or healthcare related discipline, and excellent knowledge of US and EU drug safety regulations
Associate Medical Director, Drug Safety and Pharmacovigilance (PV)
4+ years' experience in Drug Safety / Pharmacovigilance, 8+ years of industry experience, and a healthcare degree required
Senior Manager, Clinical Operations
Clinical Operations experience, Bachelor’s degree or higher, ICH-GCP guidelines, early to late Phase clinical trials
Director, Market Access Marketing
10+ years of experience, Bachelor’s degree required, experience in market access marketing, payer/organized customer/reimbursement strategy
Senior Director, Drug Metabolism and Pharmacokinetics (DMPK)
12+ years of DMPK experience, D. in Pharmaceutical Sciences, and proven track record in small-molecule oncology therapeutics
Associate Director, Statistical Programming
Master's degree in statistics or related field and 8+ years of SAS programming experience in a clinical trial setting
Senior Director, Clinical Pharmacology
Ph.D. in Clinical Pharmacology, Pharmacokinetics, Pharmaceutical Sciences, or related discipline, 12+ years of experience in clinical pharmacology within biopharma, including leadership in oncology or small-molecule drug development
Associate Director, Pharmacovigilance (PV) Operations
The role requires a Bachelor's degree in a relevant field and 8-10 years of experience in a biotech/pharma company, with a focus on pharmacovigilance and safety case processing
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