Sr Clinical Trial Manager

JR United Kingdom; Plymouth; On-site; GBP 50,000 - 70,000; Full time

Job summary

This role at a leading oncology-focused midsized pharma company involves managing clinical trials in compliance with regulatory standards. As a Senior Clinical Trial Manager, you will collaborate with various stakeholders to ensure the success of early-phase oncology studies, leveraging your expertise in clinical operations and relationship management.

Qualifications

• Minimum 5 years of experience in biotechnology, pharmaceuticals, or CROs.
• Strong understanding of GCP, ICH, and relevant regulations.
• Experience in clinical trial site start-up and relationship building.

Responsibilities

• Oversee clinical trial sites, ensuring compliance and quality.
• Manage CROs and ensure timely delivery of study milestones.
• Collaborate cross-functionally to meet study requirements.

Skills

Clinical operational experience

Strong communication skills

Proactive problem-solving

Knowledge in oncology

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).