Trial Manager (Maternity Cover)

TN United Kingdom; Greater London; On-site; GBP 35,000 - 55,000; Full time

Job summary

An established industry player is seeking an experienced Trial Manager to oversee the coordination of multicentre cancer trials. This role offers an exciting opportunity for a motivated individual with a background in clinical trials to thrive in a dynamic academic environment. The successful candidate will manage daily trial operations, liaise with stakeholders, and ensure effective recruitment and delivery of trials. If you are passionate about making a difference in cancer research and possess the necessary expertise, this role is perfect for you.

Qualifications

• Experience in clinical trial coordination is essential.
• Understanding of GCP, data protection, and research governance is required.

Responsibilities

• Manage day-to-day operations of clinical trials including set-up and recruitment.
• Coordinate data management and biological sample collection activities.

Skills

Clinical Trial Coordination

Stakeholder Liaison

Data Management

Biological Sample Collection

Education

First Degree in Biological Science

Equivalent Qualification in Social Science

Nursing Qualification

Job description

We would like to appoint an experienced Trial Manager to be responsible for:

1. Day-to-day management of the trial(s) through set-up, recruitment, and reporting;
2. Liaison with stakeholders and participating centres to promote the trial(s) and ensure successful recruitment and delivery;
3. Coordination of data management and biological sample collection activities.

The post offers an excellent opportunity for an enthusiastic and well-motivated individual with clinical trial experience to work in a dynamic and supportive academic environment at one of the leading National Cancer Research Institute cancer trials units. The successful applicant will be responsible for the central coordination of multicentre cancer trials.

Key Requirements

Applicants should hold a first degree or equivalent qualification in biological science, social science, or other relevant subject (including nursing and healthcare disciplines), or have equivalent relevant work experience. They should also have a good understanding of the principles of GCP, data protection, and research governance. Experience of clinical trial coordination is essential.