Precision For Medicine

Precision for Medicine is a specialized scientific services company that helps pharmaceutical and life sciences clients innovate, develop, and commercialize next-generation medical products. With a diverse team of experts, they offer comprehensive serv...

Pharmaceuticals

Health Care

1K-5K (1750)

Founded 2012

$225M raised

132 open positions

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Senior Project Manager - Clinical Trials

1 hour, 39 minutes ago

United Kingdom

Full-time

Senior

Project Manager

Project and Program Management

GCP

Apply Now

Precision For Medicine

Pharmaceuticals

1K-5K

Founded 2012

$225M raised

View All Jobs 132

Description

Lead full-service clinical projects in line with study budget and scope of work.
Serve as the primary client point of contact and support proposal activities and client presentations.
Manage clinical trials through all stages, from proposal strategy and costing to bid defense and study closeout.
Oversee all functional areas of the project, including data management, safety, clinical, medical monitoring, and biostatistics.
Coordinate cross-functional project teams and collaborate with internal and external stakeholders, including senior leadership and sponsors.
Prepare project status updates, deliverables tracking, performance metrics, and escalation reports for clients and management.
Review and prepare protocols and key study documents, including project plans, informed consents, site contracts, and budgets.
Support efficient trial execution while maintaining quality, timelines, scope, and financial objectives.
Potentially manage international trials and coordinate travel as needed.

Requirements

Degree or equivalent life science qualification, or an equivalent combination of education and experience.
5 to 7 years of industry experience, including at least 4 years of full-service project management experience in a clinical trial setting at a CRO.
Previous experience in a full-service, global Project Management role in the CRO industry is essential.
Experience managing oncology studies is required; experience in rare diseases or CNS is also relevant.
Working knowledge of GCP/ICH guidelines and the clinical development process.
Ability to communicate effectively in English, both written and spoken.
Strong presentation skills.
Proven computer skills with MS Office, MS Project, and PowerPoint, plus experience with CTMS, eTMF, EDC, and IXRS.
Ability to build positive working relationships with internal and external teams.
Ability to travel domestically and internationally, including overnight stays.
Core understanding of medical terminology and clinical trial activities related to clinical development plans.

Benefits

Join a supportive, collaborative, people-focused CRO environment.
Work in a high-energy team that values challenge, detail, and teamwork.
Opportunity to contribute to groundbreaking oncology and rare disease research.
Work-life balance is promoted.
Team development and employee appreciation are encouraged.

Interested in this position?

Apply directly on the company website

Apply Now

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