Gemini Staffing Consultants

We help our clients secure valuable expertise in an efficient and flexible manner due to our well-honed, industry-focused processes that is unrivaled in its transparency and competence.

Our process is unrivaled in its transparency and competence, and our history has borne this out. We are 100% focused on the Life Sciences community, providing the best quality candidates.

More and more CRO’s turn to Gemini Staffing Solutions, whether they are seeking a single individual or an entire team for their clinical trials projects on a contract, contract to hire, or permanent basis. Our industry knowledge and connections allow us to support our clients by assessing their requirements and tailoring optimized custom solutions that […]

The Clinical Data Management organization holds the overall responsibility of collecting data from the clinical trials and ensuring its accuracy, reliability and availability. They oversee the development of data collection tools to ensure that the data supports the efficacy and safety conclusions that are drawn from the clinical trial.

You are informed of the company, role, expectations, location and compensation of any role for which you wish to be presented. There is no such thing as a “blind submittal” at our company; you receive full disclosure. Since the day we opened our doors, we have never sent a candidate’s CV to a client without […]

The combination of our combined industry knowledge and connections allows us to support our clients by assessing their requirements and tailoring optimized custom solutions that meet the specific needs of their projects and initiatives.

Poring through pages and pages of clinical research job postings, applying accordingly and hoping for a positive outcome can be tedious, time consuming and, most of all, fruitless. By aligning yourself with our organization, you will immediately have access to biotechnology jobs that you never knew existed.

We are 100% committed to providing recruiting services to the Life Sciences community that leave both clients and candidates wholly satisfied with our process, approach, professionalism and, most importantly, our level of integrity. The results will typically follow if we adhere to those four core concepts, and our history has shown extraordinary results.

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: […]

The Quality Assurance organizations are comprised of people with titles such as: Manager/Director/Vice-President of Quality Assurance; Quality Assurance Specialist I,II; Quality Assurance Associate I/II; Principal Quality Assurance Specialist Associate. Additionally, there are compliance functions that reside in the Quality Assurance organization whose purpose is to ensure compliance with GMP (Good Manufacturing Practices), GLP (Good Laboratory […]