Senior Project Manager- Expanded Access Programs

Planet Pharma
London, UK
25 days ago
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Role details

Contract type
Temporary to permanent
Employment type
Full-time (> 32 hours)
Experience level
Expert
Experience required
2 years minimum
Compensation
£50,000.0 - £60,000.0
Working hours
Regular working hours

Tech stack

Clinical Trial Management Systems Microsoft Office Change Tracking GXP

Job description

We’re seeking a proactive and experienced Senior Project Manager to lead the planning, execution, and oversight of global access-related programs, including Expanded Access and Post-Approval Named Patient initiatives. This role plays a vital part in improving patient outcomes and advancing global healthcare solutions.

You’ll thrive in a collaborative, mission-driven environment that encourages innovation, values diverse perspectives, and supports continuous growth and impact in the clinical research landscape.

What You’ll Do

  • Lead the full lifecycle of regional and global projects, from start-up to close-out, in accordance with organizational SOPs and applicable policies.
  • Create, maintain, and manage project plans, budgets, and timelines while tracking changes in scope through formal Change Orders.
  • Provide operational leadership to cross-functional teams, supporting training and ongoing performance.
  • Act as a primary point of contact for clients, fostering positive relationships and ensuring high service standards.
  • Identify, monitor, and mitigate project risks, communicating effectively across teams and stakeholders.
  • Support new business activities by participating in client proposal meetings and assisting with contract development.
  • Contribute to internal process documentation and standardization across programs.
  • Supervise and support direct reports, conducting performance evaluations and professional development.
  • Oversee and audit essential project documentation in systems such as eTMF and CTMS.
  • Stay informed of current regulatory guidelines (US, UK, EU) and standards (GXP/ICH) relevant to Access Programs and clinical research.

Requirements

  • Bachelor’s degree in a relevant field (Health or Life Sciences preferred).
  • Minimum 4 years of experience in project management or clinical research, ideally within a CRO or life sciences setting.
  • At least 2 years of hands-on experience managing clinical programs or studies.
  • Excellent organizational, communication, and leadership skills.
  • Proficiency in Microsoft Office applications.
  • Willingness to travel up to 20% if needed.

Benefits & conditions

  • Long-term illness cover
  • Pension scheme with salary sacrifice
  • Generous annual leave
  • Paid maternity & paternity leave

Culture & Values

We’re committed to building an inclusive, supportive workplace where every individual can thrive. From global health impact to employee well-being initiatives, we empower our team to contribute meaningfully-and grow while doing it.

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