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Associate Director, Clinical Trial Manager

Apsida Life Science

London

On-site

GBP 85,000 - 110,000

Full time

3 days ago
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Job summary

A leading global CRO seeks an Associate Director, Clinical Trial Manager in London. This role is pivotal for overseeing full service clinical trials, managing day-to-day operations, timelines, and deliverables. Ideal candidates will have extensive CRO experience, with a strong background in Oncology, Cardiovascular, or GI.

Benefits

10% annual bonus
LTI, stock options
Annual grants

Qualifications

  • Experience working for a CRO required.
  • 5+ years in a Clinical Trial Manager or Clinical Project Manager position.

Responsibilities

  • Oversee daily operations of clinical projects.
  • Act as primary contact for sponsors.
  • Manage project timelines and deliverables.

Skills

Clinical Trial Management
Sponsor Contact
Project Planning
Risk Assessment

Job description

Associate Director, Clinical Trial Manager
Associate Director, Clinical Trial Manager

Location: London (4 days in office, 1 day from home)

Job title: Associate Director, Clinical Trial Manager

Reporting into: VP of Clinical Operations

Apsida Life Science is exclusively partnering with a leading global CRO that is looking to appoint an Associate Director, Clinical Trial Manager to be based in London. The Associate Director Clinical Trial Manager will act as the project lead for multiservice full service global clinical trials. The position interacts with sponsors and manages the timeline and all project deliverables.

Responsibilities:

  • Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
  • Serve as primary Sponsor contact for operational project-specific issues and study deliverables
  • Maintain in depth knowledge of protocol, therapeutic area, and indication
  • Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided
  • Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
  • Develop operational project plans
  • Manage risk assessment and execution
  • Responsible for management of study vendor
  • Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables

We are looking for:

  • Experience working for a CRO
  • Experience in either Oncology, Cardiovascular or GI
  • 5+ years in a Clinical Trial Manager or Clinical Project Manager position for a full service CRO that is looking to take a step up!

What’s on offer:

  • £85,000 - £110,000 per year
  • 10% annual bonus
  • LTI, stock options
  • Annual grants

If you’re interested in learning more, please reach out to Jamie Salmon from Apsida Life Science.

www.apsida.co.uk

Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK), Boston (USA) & Pretoria (South Africa) that is dedicated to delivering the best talent to the Life Science industry. We believe there is a gap in the market for a cost effective, high quality and trusted recruitment service that puts the candidate journey at the heart of the recruitment process.

Seniority level
  • Seniority level
    Not Applicable
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Project Management
  • Industries
    Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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