Senior Project Manager at WEP Clinical
Remote, Scotland, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

12 Aug, 25

Salary

0.0

Posted On

12 May, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

Are you looking for an exciting and fulfilling new position? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring forward ideas that make a real difference. Be part of a mission-driven organization dedicated to advancing clinical research and transforming lives.

Responsibilities

ROLE OBJECTIVES:

The WEP Clinical Senior Project Manager is responsible for the oversight and/or management of the setup, implementation, and management of Expanded Access Programs (EAP), Post Approval Named Patient Programs (PA-NPP), and/or other clinical research projects.

WHAT YOU’LL DO:

  • Oversee and manage the set-up, execution, and close-out of regional and global projects in compliance with WEP Clinical SOPs and Policies
  • Develop, maintain, and ensure compliance with project plans, including timelines and budgets, and track out-of-scope services in Change Orders
  • Provide leadership, training, and operational oversight for the project team
  • Build and maintain positive client relationships
  • Identify, evaluate, monitor, and mitigate risks to project quality and communicate these risks to internal team members, upper management, and clients
  • Participate in proposal meetings for potential clients and support Business Development with contracts
  • Assist in developing, documenting, and updating internal WEP Clinical procedures and processes for consistency across programs
  • Serve as a line manager for direct reports, including training, development, and performance reviews
  • Audit the compilation and completion of the eTMF and CTMS, ensuring timely filing and data entry
  • Maintain up-to-date knowledge of US, UK, and EU regulations as well as GXP/ICH Guidelines for EAP/PA-NPP and clinical research
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