Project Manager - Technical - UK

TN United Kingdom; United Kingdom; On-site; GBP 50,000 - 90,000; Full time

Job summary

An established industry player is seeking a Project Manager to oversee clinical trials and ensure quality data delivery. This role involves leading innovative projects in R&D, managing global study aspects, and collaborating with cross-functional teams. The ideal candidate will have extensive experience in clinical trial management, strong leadership skills, and a proactive approach to risk mitigation. Join a dynamic environment where your contributions will help make a positive impact on global health outcomes.

Qualifications

• 3+ years of experience in clinical trial management or related field.
• Leadership experience in managing study teams and CROs.

Responsibilities

• Lead and coordinate clinical trials from start to finish.
• Provide quality oversight and ensure timely data delivery.
• Collaborate with teams to resolve issues and drive decision-making.

Skills

Clinical Trial Management

Project Management

Risk Mitigation

Data Interpretation

Communication Skills

Problem-Solving

Education

MS/PhD in relevant field

BS/Nurse degree

Job description

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Project Manager - Technical - UK, United Kingdom

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Client:

Thermo Fisher Scientific

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

7c8e5bcd5e84

Job Views:

3

Posted:

05.05.2025

Expiry Date:

19.06.2025

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Job Description:

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. Our work spans laboratory, digital, and decentralized clinical trial services, conducted in over 100 countries. Your dedication to quality and accuracy will help improve health outcomes for communities worldwide.

Location/Division Specific Information

This role will be embedded within a client dedicated team, working alongside experienced client personnel and PPD colleagues to deliver innovative clinical support.

Discover Impactful Work:

• Provide quality oversight to the CRO and related deliverables for study execution.
• Lead and coordinate the execution of clinical trials from start-up to database close, ensuring timely and quality data delivery.
• Lead and support the setting of recruitment targets and milestones, acting as the single point of accountability for study plans.
• Collaborate with functional lines and CROs to resolve site-level issues.
• Drive decision-making and work with Clinical Project Managers on operational strategies.
• If multiple Study Managers are assigned, act as the lead and coordinate their activities.

A day in the Life:

• Drive software, AI, automation, or data analytics projects in R&D.
• Manage all study aspects globally for assigned studies.
• Plan project milestones and manage change effectively.
• Develop innovative solutions to advance R&D.
• Develop detailed study start-up and monitoring plans, and oversee study delivery.
• Conduct feasibility assessments and review site activation plans.
• Lead risk planning for sites and subjects.
• Contribute to the Clinical Trial Budget development.
• Prepare for inspections related to study management and site readiness.
• Review or produce informed consent documents as needed.
• Expand study design documents into approved protocols, incorporating input from various team members.

Keys to Success:

Education:

• MS/PhD with at least 3 years of proven experience.
• BS/Nurse with at least 5 years of proven experience.
• Extensive global clinical trial/study management experience.
• Knowledge of Good Clinical Practices, monitoring, and regulatory operations.

Experience:

• Expertise in technology areas, driving innovation and efficiency.
• Leadership experience in study management.
• Oversight of CROs.
• Experience managing costs and projections.

Knowledge, Skills, Abilities:

• Vendor collaboration skills.
• Ability to interpret data and assess risks.
• Proactive risk mitigation skills.
• Feasibility assessment skills.
• Cultural awareness and interpersonal skills.
• Problem-solving skills.
• Excellent communication skills in English.
• Attention to detail and technical expertise in data management.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Join us at PPD, part of Thermo Fisher Scientific, where diverse experiences and perspectives are valued.