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Director of Client Services (San Francisco)
Director, Client Services (Business Development - Clinical Development & CRO Services)Fully Remote | Life Sciences Consulting / CROWe are seeking a Director, Client Services with a strong focus on sales and business development to drive growth across our clinical development and CRO services portfolio. This individual will play a pivotal role in ex...
Director of CMC QA
Director / Senior Director, CMC Quality AssuranceManhattan, NY (Onsite, 5 days/week)Clinical‑Stage BiotechFull-Time | High‑Impact Individual ContributorA rapidly growing clinical‑stage biotech is seeking a Director / Senior Director of CMC Quality Assurance to lead QA activities across drug substance, drug product, analytical, labeling, packaging,...
Inside Sales Oncology
Inside Sales Oncology - Remote (Detroit preferred) $100K-$140K base + quarterly bonus | Full benefits packageA growing, patient-focused biopharmaceutical company is looking to add an Inside Sales Account Representative to its U.S. team. This is a remote role supporting oncology and rare disease customers, with strong visibility across a commercial ...
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Medical Writer
Medical Writer - Sales Training & Promotional Medical EducationUSA Based - Remote | Full-TimeAn award-winning, independently owned medical communications agency is seeking a Medical Writer to join its growing team supporting sales training, promotional medical education, and commercial learning initiatives for leading pharmaceutical and biotechnolo...
Sr. CRA
Senior Clinical Specialist$120k-$150k | Bay Area, CA | 3 days on-siteWe're working with a growing, science-driven biopharmaceutical company focused on developing innovative therapies across rare and complex diseases. With a strong global footprint and a collaborative, cross-functional culture, this organization is scaling its Clinical Affairs team ...
Director US Regulatory Affairs
Director, US Regulatory Affairs Position SummaryThis role is responsible for providing strategic regulatory leadership and oversight for U.S. regulatory activities across a clinical-stage portfolio. The individual will lead the preparation, execution, and lifecycle management of regulatory submissions, including clinical, nonclinical, and commercia...