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

86 open positions

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Clinical Trial Manager

8 hours, 1 minute ago

Serbia, Slovakia, United Kingdom, Hungary, Poland, Romania

Full-time

Senior

Program Manager

Project and Program Management

GCP

Apply Now

Precision For Medicine

Pharmaceuticals

1K-5K

Founded 2012

$225M raised

View All Jobs 86

Description

Manage the clinical and operational delivery of trial activities including site selection, start-up, enrollment management, site engagement, monitoring, data cleaning, and close-out.
Oversee assigned studies to ensure trial deliverables are completed on time and within scope.
Coordinate regulatory documentation and ongoing study oversight in collaboration with cross-functional team members.
Lead CRAs in maintaining high-quality site oversight, monitoring, regulatory, investigational product, payment, and correspondence activities.
Mentor and train team members to support study execution and team capability.
Identify risks, timeline challenges, and deliverable issues, and propose creative action plans to the sponsor and internal team.
Maintain team focus on study priorities through effective cross-functional communication and partnerships to support client satisfaction.
Serve as the central point of contact for studies and provide consultative trial management support.

Requirements

Bachelor’s degree or equivalent combination of education and experience in a science or health-related field, including oncology experience.
Significant clinical trial management experience in oncology.
Demonstrable experience leading clinical aspects of studies across multiple countries in a CRO, pharma, or biotech environment in a clinical lead role.
Working knowledge of GCP/ICH guidelines and the clinical development process.
Availability for domestic and international travel, including overnight stays.
Ability to communicate effectively in English.
Demonstrated computer skills with MS Office, MS Project, and PowerPoint.
Experience with clinical trial systems such as CTMS, eTMF, EDC, and IXRS.
Ability to build positive working relationships with internal and external stakeholders.
Strong understanding of medical terminology and clinical trial activities related to clinical development planning.
Mastery knowledge of ICH-GCP, Precision SOPs, and regulatory guidance, with the ability to implement them.

Benefits

Remote work available in the UK, Hungary, Poland, Romania, Serbia, or Slovakia.
Opportunity to work on precision medicine and oncology studies with advanced biomarker and data analytics solutions.
Exposure to novel clinical trial designs and targeted, adaptive clinical trial execution.
Work in a role with significant ownership, autonomy, and responsibility.
Collaborative environment with support for continued growth, mentoring, and training.

Interested in this position?

Apply directly on the company website

Apply Now

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