Sr Clinical Trial Manager

JR United Kingdom; Chester; On-site; GBP 55,000 - 80,000; Full time

Job summary

A leading Oncology-focused midsized pharmaceutical company seeks a Senior Clinical Trial Manager to oversee early phase trials in the UK. The role involves ensuring compliance with protocols and regulatory requirements, collaborating with cross-functional teams, and managing clinical trial sites effectively. Candidates should have a minimum of 5 years of relevant experience, a strong understanding of GCP and ICH guidelines, and the ability to build relationships with clinical sites. This position offers the chance to impact critical oncology studies.

Qualifications

• Minimum of 5 years of clinical operational experience in biotechnology, pharmaceuticals, and CROs.
• Strong understanding of GCP, ICH, GDP, and relevant CFRs.
• Previous experience as a Clinical Research Associate (CRA).

Responsibilities

• Oversee clinical trial sites from start-up to close-out, ensuring compliance with protocol and regulations.
• Collaborate with Project Managers and vendors to manage clinical studies effectively.
• Track site visit metrics and conduct compliance evaluations.

Skills

Clinical operational experience

GCP and ICH guidelines knowledge

Communication skills

Relationship-building

Proactive problem solving

Job description

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Oncology-Focused Midsized Pharma Company - Early Phase

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

Summary

The Senior Clinical Trial Manager oversees clinical trial sites from start-up to close-out, ensuring compliance with the study protocol, ICH guidelines, Good Clinical Practices (GCP), and regulatory requirements. They collaborate with the Clinical Project Manager (CPM), CRO representatives, and vendors to manage clinical studies effectively. Additionally, they may supervise Clinical Trial Managers to ensure deliverables are met on time, within budget, and to quality standards.

• Participate in the planning, implementing, and managing of clinical trials in compliance with industry regulations and ICH-GCP. - Oversee CROs and clinical trial sites, ensuring timely delivery, meeting recruitment targets, and producing high-quality data.
• Track site visit metrics, data quality concerns, and protocol deviations; conduct oversight visits for compliance evaluation. - Assist in initiation visits to confirm site training and foster relationships among sponsors, CROs, and investigators.
• Review CRA monitoring reports to ensure protocol and operational compliance; escalate issues for resolution.
• Collaborate with teams for efficient study start-up, identifying risks and ensuring timelines are met.
• Act as a subject matter expert on assigned protocols and manage CRO/site during start-up activities, including contract negotiations and document collection.
• Could you provide direction to ensure consistency in Clinical Operations processes across trials and regions?
• Work cross-functionally with departments to meet study requirements and timelines.
• Contribute to developing and reviewing study-related documents and deliver trial-specific training.
• Monitor open action items and data trends, addressing issues with CROs to enhance study execution and efficiency.
• Develop and oversee patient recruitment and retention strategies, acting on any deviations from the plan.

Experience

• Minimum of 5 years of clinical operational experience in biotechnology, pharmaceuticals, and CROs.
• Strong understanding of GCP, ICH, GDP, and relevant CFRs; familiarity with MHRA, EMA, and international regulations is a plus.
• Experience with clinical trial site start-up and initiation.
• Proven ability to build and maintain relationships with clinical trial sites and Principal Investigators.
• Strong communication skills for coordinating activities with internal teams, sites, and vendors.
• Proactive in identifying project challenges and proposing corrective actions with minimal supervision.
• Capable of working independently and delivering high-level presentations.
• Knowledge and experience in oncology.
• Previous experience as a Clinical Research Associate (CRA).