Associate

Current Associate Pharmaceutical Jobs and Articles

CRA in Belgium

We are currently recruiting for CRA / SCRA to join us for this office based role in Belgium ASAP.  As a member of the clinical operations team, you will be at the forefront of clinical trials p

CRA Associate, Italy on 9 month Contract

Our Medium-Large CRO client is looking for a Freelance CRA or Senior CRA to initiate, monitor and lead a phase II study in Italy. You will be the point of contact for the client in Italy and will work

CRA Associate, 9 month contract in Spain

An exciting opportunity for the right candidate to further their experience in the field of Oncology as a CRA, Associate working for an initial contract of 9 months,in Spain. This position is both hom

CRA, Associate, Freelance in Belgium

An exciting opportunity for the right candidate in role of CRA, Associate on a 9 month contract initially, for a Medium to Large CRO client. This position is based in Austria in the field of Oncology.

Freelance CRA

We are currently recruiting for CRA's to join us home based in Belgium.  As a member of the clinical operations team, you will be at the forefront of clinical trials practice, implementing and mo

Clinical Scientist

Job function: Production of a range of clinical documents for sponsor and external regulatory review Assists development and implementation of department mission, goals and objectives Responsib

Clinical Research Associate (CRA)in the Netherlands

  An excellent opportunity has arisen at a global Clinical Research Organisation (CRO) for an experienced Clinical Research Associate (CRA). You should have at least 2 years monitoring experien

Clinical Trial Associate in Germany

My client, an international company seeks two contract Clinical Trial Associates (CTA) for urgent office based roles near Dusseldorf, Germany. These are 12 month contracts at a minimum of 0.5 FTE and

Medical Writer in UK , Home based

An excellent opportunity for a long term contract as a medical writer for a large pharma company.  RESPONSIBILITIES Strict Quality control of all documents Prepare clinical study reports Su

Data Management, Contract in UK

9 month contract for technical data management in North England SKILLS AND EXPERIENCE Working knowledge of Rave, IVR and ePRO SAS programming skills Knowledge of clinical data standards Strong

Search For Jobs

Search by Filter

Share