• Clinical Trials Manager - Oncology Uxbridge
  • i-Pharm Consulting in Uxbridge, , United Kingdom
  • jobs
  • 1 week ago

jobs description

Job Title: Clinical Trials Manager - Oncology
Location: Uxbridge, UK
Pay Rate: £420 - £440/day (Inside of IR35)
Contract Length: 12 Month Contract
Work Structure: Monday - Friday, 3 days/week on site required.

Are you ready to make a difference in the world of oncology clinical trials? Join a leading research-based bio-pharmaceutical company committed to creating a healthier world. Our client's focus is on delivering life-saving therapies to patients in need, and we are looking for a dedicated Clinical Trials Manager to join their team at Uxbridge, UK.

Position Overview:

In this role, you will be part of the Clinical Operations team responsible for the worldwide execution of Phase I-IV clinical trials across various therapeutic areas. You will manage a geographical region(s) of assigned clinical studies or multiple components of larger studies, typically focusing on Phase I or smaller studies.

Some of the responsibilities include:
• Manage all components of small clinical studies... including Phase I studies.
• Lead contract research organisation (CRO) and vendor selection, manage interactions and deliverable.
• Serve as the key operational contact for studies, overseeing site evaluations, initiations, close-out visits, and routine monitoring.
• Manage study time lines, documentation, and communications.
• Participate in and manage project meetings and conference calls with CROs, vendors, and cross-functional teams.
• Oversee study sites/region and review routine regulatory documents to ensure compliance.
• Assist in training new or less experienced colleagues.

Minimum Education & Experience:
• PharmD / PhD with 2+ year's relevant clinical or related experience in life sciences.
• MA / MS with 3+ year's relevant clinical or related experience in life sciences.
• BA / BS / RN with 5+ year's relevant clinical or related experience in life sciences.
• Multiple year's clinical or related experience in life sciences, including experience leading or managing less complex studies and project teams.
• Experience managing the work of external vendors.

Knowledge & Other Requirements:
• Demonstrated ability to be a fast learner.
• Flexible and adaptable to change, able to move between projects easily and provide support/expertise where needed.
• Ability to manage any component of full cycle study management, from start-up to close-out.
• Advanced knowledge of study management best practices and tools.
• Thorough knowledge of FDA, EMA, and other applicable national regulations, ICH guidelines, and GCP.
• Familiarity with standard medical/scientific terminology.
• Clear and concise communication skills.
• Ability to support a team-oriented, highly matrixed environment.
• Ability to execute multiple tasks as assigned.
• Willingness to travel when needed.

How to Apply:

If you possess the expertise and qualities required for this challenging yet rewarding role, please submit your application including your CV to [email protected] or press the apply button below!

Please note: You must be able to work in the UK without restriction or sponsorship to be eligible for this role. If you are interested in finding out more about this role or others, please contact Jada Kirlew at [email protected] or call: +44 (0)20 7551 0727 (UK) +31 208 089 982 (NL
Uxbridge UK


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