Financial Study Start-Up Project Manager (London)

Fortrea

Maidenhead

Hybrid

GBP 65,000 - 95,000

Full time

14 days+

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Job summary

Fortrea is seeking a Study Start-Up Project Manager to join our UK team. You will be dedicated to a leading global pharmaceutical company, focusing on budget and contract negotiations, and ensuring timely start-up milestones within the UK.

The role requires strong negotiation and risk management, excellent English communication, and the ability to work in a hybrid environment, coordinating with investigators, vendors, and country managers across multiple deliverables.

Qualifications

  • Proven expertise in budget and contract negotiations within a clinical trial setting.
  • Strong problem-solving abilities with proactive risk mitigation.
  • Experience managing challenges affecting protocol timelines and regulatory compliance.
  • Excellent communication and negotiation skills to influence stakeholders at all levels.
  • Ability to work effectively in a hybrid environment while managing multiple deliverables.

Responsibilities

  • Lead budget and contract negotiations with a deep understanding of the local regulatory environment and its implications for study start-up activities.
  • Address and resolve issues by indirectly influencing investigators, vendors, external partners, and country managers with minimal support.
  • Independently make decisions with limited oversight while proactively developing risk management and mitigation strategies for the country.
  • Ensure compliance with local regulations, quality standards, and protocol milestones during the start-up phase.

Skills

Budget negotiations
Contract negotiations
Risk management
Stakeholder management
Communication
Leadership
Hybrid work

Job description

Location: Hybrid (2 days per week in the Central London office)

We are seeking a Study Start-Up Project Manager to join our team. In this role, you will work 100% dedicated to a leading global pharmaceutical company, playing a critical part in the successful initiation of clinical trials within the UK. Your primary focus will be on budget and finance tasks , including contracts and budgeting, with significant influence on meeting country-specific trial commitments and objectives during the start-up phase.

Key Responsibilities
  • Lead budget and contract negotiations with a deep understanding of the local regulatory environment and its implications for study start-up activities.
  • Address and resolve issues by indirectly influencing investigators, vendors, external partners, and country managers with minimal support.
  • Independently make decisions with limited oversight while proactively developing risk management and mitigation strategies for the country.
  • Ensure compliance with local regulations, quality standards, and protocol milestones during the start-up phase.
Qualifications and Core Competencies
  • Proven expertise in budget and contract negotiations within a clinical trial setting.
  • Strong problem-solving abilities, with a proactive approach to identifying and mitigating risks.
  • Experience in managing common challenges such as: Quality and compliance concernsLegal issuesDeliverable-specific risks impacting protocol timelines
  • Exceptional communication and negotiation skills, with the ability to influence and mentor stakeholders at all levels.
  • Demonstrated ability to work effectively in a hybrid environment while managing multiple deliverables and protocols simultaneously.
Behavioral Expectations
  • Highly organized, with strong coordination skills to manage complex tasks and priorities.
  • Ability to analyze root causes of issues and propose practical solutions, including escalating to management when needed.
  • Proficient in English, with excellent written and verbal communication skills.
  • Collaborative mindset and leadership capabilities to influence diverse teams across various functions.

If you are a motivated professional with a strong background in study start-up activities, this role offers an excellent opportunity to make a meaningful impact in clinical research.

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