Clinical Research Manager (Oncology) - UK - FSP

TN United Kingdom; Greater London; Remote; GBP 50,000 - 75,000; Full time

Job summary

A leading company in clinical research is seeking a Clinical Research Manager (Oncology) to oversee oncology clinical trials. This role involves project management, stakeholder communication, and ensuring compliance with regulations. Ideal candidates will have a degree in life sciences and experience in clinical trials.

Qualifications

• Experience leading clinical trials or coordinating clinical research.
• Clinical or management experience in healthcare or clinical research.

Responsibilities

• Support, coordinate, and conduct oncology clinical trials.
• Manage study start-up activities and lead project teams.
• Ensure compliance with ICH/GCP and local regulations.

Skills

Leadership

Communication

Customer focus

Education

Degree in life sciences

Nursing

Job description

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Clinical Research Manager (Oncology) - UK - FSP, Harrow

Client: Parexel

Location: Harrow, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: fd36f94832bb

Job Views: 3

Posted: 17.05.2025

Expiry Date: 01.07.2025

Job Description:

When our values align, there's no limit to what we can achieve.

Register your interest for a home-based (oncology focused) Clinical Research Manager role with Parexel FSP in the UK.

At Parexel FSP, people make a difference. We aim to prevent and cure disease by delivering new medicines and therapies to patients. Our success relies on the expertise, innovation, and commitment of our global team.

You will support, coordinate, and conduct sophisticated oncology clinical trials for our client, a top 10 Pharma company. This includes study start-up, maintenance, and closure, as well as vendor management and CRA oversight.

The Clinical Research Manager (CRM) is responsible for end-to-end project management, ensuring compliance with ICH/GCP, local regulations, client policies, quality standards, and adverse event reporting.

Key Accountabilities:

• Communicate effectively with internal and external stakeholders and vendors.
• Prioritize tasks and respond to urgent requests promptly.

Project Initiation & Planning:

• Manage study start-up activities.
• Contribute to project planning tools and site selection strategies.
• Develop site selection, monitoring, patient recruitment, and retention plans.
• Create study plans, tools, and forms.

Project Implementation, Control & Evaluation:

• Lead project teams and evaluate resource needs.
• Address site issues and monitor study progress, recruitment, retention, and data quality.
• Ensure quality and implement process improvements.
• Assist in financial forecasting and may conduct site visits.

Project Close-out:

• Coordinate database lock and final documentation.
• Participate in end-of-study reviews and lessons learned.

Skills:

• Leadership: Lead virtual teams, negotiate, influence, and make decisions in ambiguous situations.
• Personal: Initiative, independence, high-quality work, excellent communication and presentation skills.
• Business/Operational: Customer focus, deep understanding of clinical trial processes, knowledge of SOPs, ICH-GCP, and regulations.

Knowledge and Experience:

• Proficiency in English and local language as required.
• Clinical or management experience in healthcare or clinical research.
• Experience leading clinical trials or coordinating clinical research.

Education:

Degree in life sciences, nursing, or relevant clinical/management experience.

If you have experience leading clinical trials, working as a CRA, and possess project or people management skills, we offer a promising future involving international development and advancement into high-level roles. Some travel may be required despite the home-based nature of the role.