Senior Clinical Trial Manager at TFS HealthScience

Lund, , Sweden -

Full Time

Start Date

Immediate

Expiry Date

09 Apr, 26

Salary

0.0

Posted On

09 Jan, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trial Management, Oncology, GCP, Regulatory Requirements, Site Management, Vendor Oversight, Monitoring Activities, Data Integrity, Operational Oversight, Risk Mitigation, Cross Functional Collaboration, Protocol Compliance, Phase 2 Trials, CRO Management, Site Performance, Training

Industry

Pharmaceutical Manufacturing

Description

About this role TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions. The Senior Clinical Trial Manager is responsible for providing end to end operational oversight of an oncology clinical trial, including site management, vendor and CRO oversight, monitoring activities, and ensuring trial execution in compliance with protocol, GCP, and regulatory requirements. As part of our SRS/FSP team, you will be dedicated to one sponsor, a global biotechnology company that is an industry leader in oncology drug development with a growing European clinical footprint. Key Responsibilities: Provide operational oversight and execution of a global Phase 2 oncology clinical trial across multiple European countries Manage and oversee CROs, vendors, and site level activities to ensure high quality trial delivery Support site selection, start up, initiation, training, monitoring, and ongoing site performance Review monitoring reports and ensure timely resolution of site issues, protocol deviations, and action items Collaborate closely with Medical Monitors, data management, and cross functional teams to support safety oversight and data integrity Maintain accurate and inspection ready trial documentation and proactively identify and mitigate operational risks Qualifications: Bachelor of Science in Life Sciences or equivalent Minimum 5 to 8 years of experience as a Clinical Trial Manager or Senior Clinical Trial Manager Experience working on global Phase 2b or Phase 3 clinical trials Oncology experience is required Strong knowledge of ICH GCP, regulatory requirements, and clinical trial operations Additional Information The role is linked to the Lund area, with flexibility regarding remote working and on site presence Travel within Europe is required as part of the role for site related activities Full time, permanent position What We Offer We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients A Bit More About Us Our journey began over 27 years ago in Sweden, in the city of Lund. As a full service, global Contract Research Organization (CRO), we build solution driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology. Our core values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.

Responsibilities

The Senior Clinical Trial Manager is responsible for providing end-to-end operational oversight of an oncology clinical trial, including site management and vendor oversight. They ensure trial execution in compliance with protocol, GCP, and regulatory requirements.