Study Manager - Clinical Operations

PE Global; Greater London; Hybrid; GBP 80,000 - 95,000; Full time

Job summary

PE Global is seeking a Study Manager-Clinical Operations for a leading multi-national Pharma client in London. This role involves overseeing study execution, collaborating with various teams, and ensuring quality and progress updates. The position is a 6-month contract with hybrid work options, offering competitive daily rates.

Qualifications

• 7 years’ work experience in life sciences or medically related field.
• At least 4 years experience within the Biopharmaceutical industry.
• Experience in oversight of external vendors.

Responsibilities

• Overall study execution oversight.
• Provide leadership, guidance, and direction to Global Study Operations staff.
• Collaborate with cross-functional study members.

Skills

Leadership

Collaboration

Risk Management

Communication

Education

BA/BS/BSc

Job description

Direct message the job poster from PE Global

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PE Global is currently recruiting for a Study Manager-Clinical Operations for a leading multi-national Pharma client based in London.

This is an initial 6 months contract position, offering hybrid work 2 days on site and 3 days working from home.

Daily rate is £371.59 PAYE or £438.56 Umbrella.

Duties of the role/Responsibilities

• Overall study execution oversight
• Provide leadership, guidance, and direction to Global Study Operations (GSO) staff assigned to studies
• Facilitate cross-functional Study Execution Team (SET) 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

Education/Experience

• BA/BS/BSc
• 7 years’ work experience in life sciences or medically related field, including at least 4 years experience within the Biopharmaceutical industry, biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical, or CRO
• Experience in oversight of external vendors (e.g., CROs, central labs, imaging vendors, etc.

Interested candidates should submit an updated CV.

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Science

• Industries

  Staffing and Recruiting and Pharmaceutical Manufacturing

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