For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
Client is looking for a Sr. Regulatory Manager for a 12-month, remote, part-time opportunity. Expected 20hrs/week.
Biotech oncology company with three products in clinical development and six in nonclinical. Senior Regulatory Manager to assist in managing studies as a regulatory lead and putting together FDA documents, including IND submissions.
Responsibilities also include:
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