Sr Clinical Trial Manager

JR United Kingdom; Newport; On-site; GBP 50,000 - 75,000; Full time

Job summary

Une entreprise pharmaceutique de taille moyenne axée sur l'oncologie cherche un Senior Clinical Trial Manager pour superviser les essais cliniques. Le candidat idéal devra posséder au moins 5 ans d'expérience en gestion d'essais cliniques, notamment dans le domaine de l'oncologie, avec une connaissance approfondie des bonnes pratiques cliniques (GCP) et une forte capacité à établir des relations avec les sites d'essais et les enquêteurs principaux.

Qualifications

• Minimum de 5 ans d'expérience clinique opérationnelle dans les biotechnologies, la pharmacie et les CRO.
• Forte compréhension des GCP, ICH, et des réglementations internationales.
• Expérience en démarrage de sites d'essais cliniques.

Responsibilities

• Gérer les sites d'essais cliniques de la mise en route à la clôture.
• Collaborer avec le Clinical Project Manager et les représentants des CRO.
• Développer des stratégies de recrutement et de rétention des patients.

Skills

Gestion des essais cliniques

Connaissance des GCP

Communication

Gestion des relations

Analyse des risques

Job description

Social network you want to login/join with:

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).