DOCS Global

Clinical Study Co-Ordinator (home-based - UK)

Location
UK
Salary
Competitive
Posted
29 Apr 2021
Closes
29 May 2021
Ref
28823
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
Do you have a strong clinical research academic background? 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 January 2021, please read the below requirements and apply today.

The Study Co-Ordinator will be assigned a portfolio of both US and Global Real World Evidence studies to carry out the following tasks;
• Manage/Assist with PO set-up
• Schedule and Coordinate the proposal review process including Evidence Connect workflow
• Ensure compliance with data entry guidance for Evidence Connect.
• Ensure completeness of documentation in Evidence Connect to enable teams to make effective business decisions
• Manage Evidence Review Team (ERT) Proposal review process including scheduling meetings, taking minutes, and managing document upload/storage for compliance purposes
• Special projects as assigned to support the Data & Analytics Team
• Assist the tumor teams and contribute towards start-up, execution, close out and reporting of real world evidence studies
• 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
• 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
• Interface with Strategic and Operational Partners as well as internal cross-function teams to complete activities relating to the assigned processes, systems and projects
• Support tumor teams in monitoring and overseeing the operational and financial aspects of real world evidence studies (i.e. invoice approval and budget management) to ensure procurement documents are managed in the Ariba system, invoices are submitted and paid on time, serving as main point of contact with Business & Operations Leads (BOLs)
• Set-up, ongoing maintenance and closure of all study related Company tracking systems and communication tools (i.e. IMPACT, Evidence Connect, SharePoint, collaborative study folders on BOX)

If you would like to discuss in detail, apply to DOCS Global today!

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