Clinical Trials Manager

2 weeks ago

London, Greater London, United Kingdom i-Pharm Consulting Full time
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 prepared to impact the oncology clinical trials field? Join a top research-based bio-pharmaceutical company dedicated to fostering a healthier world.

Our focus is on delivering life-saving treatments to patients in need, and we are seeking a committed Clinical Trials Manager to join our team in Uxbridge, UK.


Position Overview:

In this role, you will work alongside the Clinical Operations team responsible for executing Phase I-IV clinical trials worldwide across various therapeutic areas.

You will oversee a geographical region(s) of assigned clinical studies or multiple components of larger studies, often concentrating on Phase I or smaller studies.


Key Responsibilities:

Manage all aspects of small clinical studies, including Phase I studies.
Lead contract research organization (CRO) and vendor selection, manage interactions, and deliverables.
Act as the primary operational contact for studies, supervising site evaluations, initiations, close-out visits, and routine monitoring.
Supervise study timelines, documentation, and communications.
Participate in and manage project meetings and conference calls with CROs, vendors, and cross-functional teams.
Monitor study sites/region and review routine regulatory documents to ensure adherence.
Assist in training new or less experienced colleagues.


Minimum Education & Experience:

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


Knowledge & Requirements:

Demonstrated ability as a quick learner.
Flexible and adaptable to change, able to transition between projects smoothly and offer support/expertise as needed.
Able to manage any aspect of full cycle study management, from start-up to close-out.
Advanced understanding 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 vocabulary.
Clear and concise communication skills.
Capable of supporting a team-oriented, highly matrixed environment.
Able to handle multiple assigned tasks.
Willingness to travel when required.


How to Apply:

If you have the expertise and attributes needed for this challenging yet fulfilling role, please submit your application along with your CV.
Please note: You must be eligible to work in the UK without any restrictions or sponsorship to qualify for this position.

If you would like more information about this role or others, please reach out to Jada Kirlew.

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