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Sr clinical trial manager

London
JR United Kingdom
Clinical trial manager
€100,000 - €125,000 a year
Posted: 13 June
Offer description

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Sr Clinical Trial Manager, United Kingdom

Client: Advanced Clinical

Location:

Job Category: Other

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EU work permit required: Yes

Job Views: 7

Posted: 10.06.2025

Expiry Date: 25.07.2025


Job Description:

Senior Clinical Trial Manager (via FSP)

Oncology-Focused Midsized Pharma Company - Early Phase

This role will focus on the Early Phase Oncology program in the UK and mainland Europe. Candidates must have recent experience with early-phase oncology studies at a CRO, biotech, or pharmaceutical company.


Responsibilities

* Oversee clinical trial sites from start-up to close-out, ensuring compliance with protocols, ICH guidelines, GCP, and regulations.
* Collaborate with the Clinical Project Manager, CROs, and vendors to manage studies effectively.
* Supervise Clinical Trial Managers to ensure timely, within-budget, and quality deliverables.
* Participate in planning, implementing, and managing clinical trials.
* Oversee CROs and sites, ensuring recruitment targets and high-quality data.
* Conduct oversight visits and review monitoring reports for compliance.
* Assist in site initiation, training, and relationship building.
* Manage start-up activities, including contracts and documentation.
* Ensure consistency in Clinical Operations processes across trials and regions.
* Work cross-functionally to meet study requirements and timelines.
* Develop and review study documents and deliver training.
* Monitor data trends and address issues with CROs.
* Develop patient recruitment and retention strategies.


Experience

* Minimum 5 years in clinical operations within biotech, pharma, or CROs.
* Strong knowledge of GCP, ICH, CFRs; familiarity with MHRA, EMA, and international regulations is a plus.
* Experience with site start-up and initiation.
* Ability to build relationships with sites and investigators.
* Excellent communication skills for coordinating with teams, sites, and vendors.
* Proactive problem-solving skills with minimal supervision.
* Ability to work independently and deliver presentations.
* Experience in oncology.
* Previous CRA experience preferred.
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