Quality Control & Quality Assurance

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. […]

The core competency of Gemini Staffing Consultants is providing clinical trials staffing solutions. Our deep focus on this niche provides a high level of value for our many partners in the life science industry.

Gemini Staffing provides experienced pharmacovigilance specialists to handle this all-important task, as well as other experts in all phases of clinical research and development.

Biotech, pharmaceutical, medical device, and CROs turn to Gemini Staffing for critical resources in quality assurance, regulatory affairs, and compliance functions.

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 critical resource. Gemini Staffing places highly vetted candidates for drug safety and pharmacovigilance positions.