Clinical Study Manager
JOB_53183934688864Job type
ContractLocation
LondonWorking Pattern
Full-timeSpecialism
Clinical ResearchIndustry
Scientific and R&DPay
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
Clinical Study ManagerJOB_531839346888642025-05-192025-08-18
Talk to Claire Helliwell, the specialist consultant managing this position
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JOB_53183934688864