Ref #: 28253

Employment type: Permanent - Full-Time

Location: United Kingdom, Home-based

Posted: 07-Apr-2021

Description

Have you previous clinical research experience, and you're now looking for your next role in Industry? Would you relish the chance to prove your credentials with a Global Pharmaceutical company, joining an existing team of experienced staff?
If you are looking for your next role, are happy to be home-based and have the flexibility to start in November 2020, please read the below requirements and apply today.

Role and Responsibilities;

The Study Coordinator (SC) provides administrative study/project related support for the Delivery Team, coordinating activities that ensure quality and consistency across the portfolio. The position requires an individual who works independently and in a team environment and who is experienced in processing clinical study research documents.

The position requires collaboration, ability to effectively manage multiple tasks and assignments simultaneously and excellent communication and IT skills with other internal functional areas and external contracted sites.

• Assist the study team and contribute towards start-up, execution, close out and reporting of Company Sponsored studies, start up of Early Access Programs and support for Externally Sponsored Research studies
• Lead the collection, review and tracking of Essential Documentation, key correspondence and other relevant study documentation ensuring storage, formatting and version control is compliant with Company Procedures, document retention guidelines, industry standards and the applicable laws
• Support study teams in monitoring and overseeing the operational and financial aspects of CRO/ESP collaboration (i.e. invoice approval and budget management) to ensure they are effectively undertaken, studies are delivered to plan and study conduct documented
• Lead the coordination of administrative tasks and provide operational support during study process, governance, audits and regulatory inspections, according to company policies, SOPs and regulations