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Technical Regulatory Specialist
My client is a successful, global CRO supporting leading pharmaceutical and biotech companies across the Untied States. They are seeking a Technical Regulatory Specialist to provide oversight to the team responsible for compilation, preparation, and review of all Regulatory Submissions. This role…
Principal Medical Writer - Global BioPharma - Remote
Meet's top Biopharma client has engaged us on an EXCLUSIVE new search for a talented Principal Medical Writer. This role can be fully-remote based and will be leading the completion of regulatory documents in support of their extensive development pipeline (Virology, Immunology, Oncology,…
Director, External Biologics Manufacturing - CMO Oversight - San Francisco
.Director, External Biologics Manufacturing – Exciting position has become available in a growing, fast moving global, public biopharma in their HQ in San Francisco. This individual will collaborate with CMC Senior Management and oversee all aspects of GMP manufacturing for several Biologics…
Senior Scientist - Bioanalytical (BA) Development - San Francisco
Summary Our Client is a research-based biopharmaceutical company that discovers and develops innovated medicines in high unmet medical need is looking for a Senior Scientist to join their San Francisco team! They will be responsible for supervising the analysis of clinical (PK, ADA, biomarker)…
Research Associate - CAR-T - Bay Area (Peninsula)
Summary Meet is partnering with an innovative company focused on gene editing and genetic engineering of human cells for immunotherapy. We are seeking a highly motivated, hardworking research associate in the preclinical development team. The ideal candidate will have experience with CAR- T Cell…
Principal Medical Writer- Global Biopharma - Chicago, Fully Remote
My client is a global biopharma with an extremely active pipeline with multiple compounds in Immunology, Oncology, Neuroscience, Virology, and General Medicine. My client employs almost 30,000 individuals globally across 170 countries and spends over 3.5 billion dollars on research and development…
Clinical Trial Disclosure and Transparency Lead - Global CRO - *Fully Remote* - 12+ Month Contract
Meet is partnering with a reputable midsized CRO, currently seeking a Clinical Trial Disclosure and Transparency Lead to join their growing, highly experienced global team. This role is a 12-month, fully remote contract position, with a guaranteed 40 hours of work per week. This position offers an…
Snr Scientist, Technical Operations - GMP, Exceptional Career Growth - Global Pharma
This client is an established biopharmaceutical company that manufactures plasma-derived and recombination therapeutic products. They are currently undergoing an exciting period of growth in which they are looking to expand their operations and quickly add headcount. The Senior Scientist, Technical…
Medical Editor
Meet is working with a revolutionary medical communications agency in Boston. This agency takes an entrepreneurial approach across their work in various high science areas. The agency is looking for a Medical Editor to join their growing team. They pride themselves on being an exciting workplace…
Senior CRA
The Senior Clinical Research Associate (CRA) would be responsible for performing multiple tasks with the implementation and conduct of clinical trials, focusing on the areas of trial planning, enrollment, site monitoring, data quality, and study tracking and reporting. Responsibilities include…