Regulatory Project Manager
6 days ago
We are seeking a highly skilled Regulatory Project Manager to join our team at ProductLife Group. As a key member of our clinical trials department, you will be responsible for managing projects from initial preparation to final submission and notification of results. Your expertise in regulatory affairs and clinical trials management will ensure seamless execution of projects, meeting deadlines and delivering high-quality results.
The ideal candidate will have a scientific background, with a minimum of 5-10 years of experience in clinical trials management. A strong understanding of the clinical trials environment, regulation, and good technical skills in CTA management through CTIS/Transition management are essential. Proficiency in MS Office (Word, Excel, PowerPoint) and meeting management is also required. Experience in coordination and team management, as well as eTMF (Veeva), would be an added advantage.
Salary: $80,000-$120,000 per year, depending on experience. Benefits include comprehensive health insurance, retirement savings plan, and generous paid time off. Additional benefits may include relocation assistance, professional development opportunities, and flexible work arrangements. Our company offers a dynamic and supportive work environment, where you can grow professionally and make a meaningful contribution to the success of our clients.
Based on your skills and qualifications, we estimate that you will be able to achieve this salary range. If you are a motivated and experienced professional looking for a new challenge, we encourage you to apply for this exciting opportunity.
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