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!
Including: Clinical Data Associate/Specialist Clinical Data Management/Leadership Drug Safety Associate/Specialist DS/PV Management/Leadership PV Associate/Specialist
Including: Regulatory Affairs Associate/Specialist Regulatory Operations Associate Quality Assurance Specialist GCP Auditor RA/QA Management/Leadership
Including: • Clinical Trial Coordinator/Clinical Trial Administrator • Clinical Research Associate/Monitor/regional Monitor • Clinical Project Manager/Clinical Trial Manager • Medical Writer • Clinical Operations Management/Leadership
Including: • Drug Safety Associate/Specialist • PV Associate/Specialist • DS/PV Management/Leadership • Clinical Data Associate/Specialist • Clinical Data Management/Leadership
Drug Safety/Pharmacovigilance organizations are comprised of people with titles such as: Manager/Director/Vice President of Drug Safety/Pharmacovigilance; Senior/Principal Drug Safety/Pharmacovigilance Associate/Specialist. 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. Contact us today and let Gemini […]
Regulatory Affairs organizations are comprised of people with titles such as: Manager/Director/Vice-President of Regulatory Affairs; Regulatory Affairs Associate I/II; Senior/Principal Regulatory Affairs Associate/Specialist; Regulatory Affairs Coordinator/Administrator. 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. […]
Gemini Staffing Announces New Hire
Year In Review – Recent Staffing Highlights
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
An unexpected – but welcomed – 4-legged guest!!