Pharmacovigilance consultants holds clinical trials to use best practices, protecting patients from harm and quantifying risk relative to benefit of the use of the sponsor company’s product. For these reasons, a pharmacovigilance consultant is a highly critical resource. Gemini Staffing places highly vetted candidates for drug safety and pharmacovigilance positions.
The Regulatory Affairs organization within a biotech/pharmaceutical/medical device company holds the overall responsibility of ensuring that the sponsor company adheres to and complies with all regulations and laws set forth by the United States Food and Drug Administration (FDA) pertaining to the company’s product. Regulatory Affairs organizations are comprised of people with titles such as: […]
Qualified candidates benefit from our deep industry knowledge and relationships. By aligning yourself with our organization, you will immediately have access to biotechnology jobs that you never knew existed. Let Gemini start working for you today.
Qualified candidates benefit from our deep industry knowledge and relationships. By aligning yourself with Gemini, you will immediately have access to biotechnology jobs that you never knew existed. Contact us today and let Gemini start working for you!
Year In Review – Recent Staffing Highlights
Market conditions continue to show subtle signs of improvement! New this week…
Gemini Staffing Announces New Hire
Attention Clinical Operations Directors: We have a unique opportunity with a Metro Boston-based biotech that is developing novel precision oncology programs. If you would like to learn about a company that offers what many can’t – a robust pipeline, an unrivaled veteran leadership team, a strong financial standing and a workplace that attracts and retains its people – we would love to hear from you. Please contact us today!
Featured Role – Director/Senior Director, Regulatory CMC – Remote, East Coast preferable