Job Details 
Phlexglobal
Our database has identified the following jobs as matching your search criteria. If you cannot see a job you are interested in, please search again refining your criteria or email us for further help and support.| Title | Global Studies Associate | ||
|---|---|---|---|
| Role | Clinical Trial Administrator | Reference | TL10229 |
| Location | Eastern | Working hours | Full-time |
| Salary | On application | Employment type | Contract / Interim |
| Summary | Are you a committed and talented professional looking for a pivotal role in the pharmaceutical industry? Join one of the largest pharmaceutical organisations in the industry and let Phlexglobal assist you in realising your potential. We have a Global Studies Associate role located in our client’s offices in Welwyn Garden City, Hertfordshire. Our client is one of the principal Pharmaceutical organisations and has a continually growing pipeline of exciting products, enabling you build and develop your career path whilst working on a range of diverse and challenging products. This is your chance to contribute to the development of medicines for the global community. | ||
| Description | An opportunity to be a pivotal part of a Clinical Research team. The Global Studies Associate needs to be an organised, logical, enthusiastic and methodical worker with the will to succeed. You will be responsible for the coordination and support of study and data management activities of one or more Study Management Teams to ensure the standardisation and consistency of delivery across studies in accordance with ICH GCP and best practices. Responsibilities include: ? Providing coordination and support through effective working relationships, management of all global study drug supplies, managing and distributing of study-related supplies, ensures timely return of site and feasibility data, coordinates and organises investigator and monitor meetings ? Develops, manages and maintains appropriate study documentation ? Track and maintain study information and report on study progress ? Co-ordinates activities and liaises with CROs and vendors to ensure delivery against contracted scope of work ? Provides input into the development of best practices and advises on the availability of standardised tracking tools and templates The Global Studies Associate role gives you the unique opportunity as an administrator and as a member of the Clinical Trials team to be involved in a variety of aspects of the clinical trial process. You should be a team player, self-motivated, resourceful, and able to communicate clearly and accurately, have proven organisation skills and have an eye for details. All applicants must be eligible to work in the UK. We at Phlexglobal value our employees, not only will you benefit from working with one of the leading CROs, we offer COMPETITIVE SALARIES, COMPANY CONTRIBUTORY PENSION SCHEME, PERSONALISED TRAINING and DEVELOPMENT and CAREER PLANNING to name a few. For more details please contact your Resourcing Team. Phlexglobal is a leading quality driven Contract Research Organisation who only select the best. Ours is a people culture and we are committed to nurturing and training self-motivated, exceptional Clinical Research Professionals. If this sounds like you and you have the desire, skills and tenacity to succeed within the Clinical Trials field then contact me now! If this job isn’t relevant for you but you would like to find out more about the roles we offer then please contact your Resourcing Team on 01494 720 420 ext 440 or email – Resourcing@phlexglobal.com | ||
Add to job basket | Apply for job
