Clinical Study Manager

4688864
  • Job type

    Contract
  • Location

    London
  • Working Pattern

    Full-time
  • Specialism

    Clinical Research
  • Industry

    Scientific and R&D
  • Pay

    Day rate

Exp Global CSM London

Experienced Clinical Study Manager required for 6-month contract, hybrid role (London)
Study Manager accountable for day-to-day Global Study Operations study execution and related deliverables
Key responsibilities include managing risks, issues and opportunities that impact timeline, quality, and budget, overseeing the GSO study team, vendors and CRO, as well as collaborating with cross-functional representatives to execute on study deliverables. The Study Manager may be assigned to and is responsible for managing early-stage, late-stage, or post-approval studies. The Study Manager will engage and collaborate with cross-functional team members to drive study activities and is responsible for facilitating and leading Study Execution Team (SET) activities and meetings.
Responsibilities include but are not limited to:
• Overall study execution oversight
• Provide leadership, guidance, and direction to GSO staff assigned to studies
• Facilitate cross-functional Study Execution Team meetings
• Collaborate with cross-functional study members to drive and execute on study deliverables, documents, and plans
• Proactively identify, manage, and communicate cross-functional study issues, risks and mitigations in a timely manner
• Provide regular study quality and progress updates to key stakeholders as needed
• Monitor and act upon study metrics; review trend-identification and analysis and provide targeted follow-up where appropriate
• Collaborate with other Study Managers to ensure consistency and maintenance of the various study plans within a program
• Collaborate with People and Process Managers of the Study Specialist staff to support team member productivity and career growth
• Other responsibilities Include:
o Contribute to the Study protocol and Informed Consent Form (ICF) development
o Management of Study Timelines
o Management of CRO and Vendors
o Management of Study Lifecycle (start-up, enrollment, maintenance and close-out)
o Oversight of Drug / Investigational Product (IP) process
o Management of Study Budget
o Oversight of Feasibility, Recruitment and Enrollment
• Collaborate with study managers/cross-functional team members to implement department process change and efficiencies

You will require good Global Clinical Study management experience and be available for an immediate start, (London 2 days a week).
Please send CV to claire.helliwell@hays.com

Apply for this job

Talk to Claire Helliwell, the specialist consultant managing this position

Located in London-City, 5th Floor, 107 Cheapside, Telephone 0333 010 6303
Click here to access our Privacy Policy, which provides detailed information on how we use and protect your personal information, and your rights in relation to this.