UK Clinical Project Manager

Pharmaceutical Research Associates, Inc; London; Remote; GBP 45,000 - 65,000; Full time

Job summary

A leading company in the global pharmaceutical industry is seeking an Oncology Clinical Project Manager to oversee site management and project commitments in a dynamic work environment. The ideal candidate will have a strong background in clinical research and oncology project management, ensuring high-quality data delivery and site performance. This role offers a unique opportunity to contribute to vital health initiatives while working remotely in an inclusive culture.

Qualifications

• Minimum of 4 years experience in clinical operations including project coordination.
• Experience managing culturally diverse and remote teams is required.
• Strong background in clinical research monitoring roles.

Responsibilities

• Ensure identification, qualification, and management of study sites.
• Lead the Local Study Teams and develop study strategy.
• Monitor the timely delivery of data to required quality.

Skills

Oncology project management

Client relationship management

Site management

Monitoring clinical trials

Education

Degree in life sciences

Job description

Overview

An additional UK home-based Oncology Clinical Project Manager is required to manage sites (with some CRA Line Management responsibilities) within the UK region.

You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cancer, cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines.

You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.

Responsibilities

Amongst other tasks, your main responsibilities will be to;

• Ensure that sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation is archived.
• Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality.
• Leads and optimises the performance of the Local Study Teams at country level
• Liaison with Senior Management in developing study strategy.

Qualifications

Ideal candidates will be those with Oncology project management experience in the clinical space, with a significant background in clinical research monitoring roles; the candidates operating as Clinical Project Managers would be ideal.

What is Required

• Degree (BA/BS/BSc) in life sciences
• Proven track-record in Oncology Project Management of clinical trials within the Clinical Research industry
• Clinical Project Managers with a CRA background
• Must have demonstrated strong client relationship management skills
• Must be able to manage culturally diverse and practically remote teams

Education and Experience requirements:

Minimum of 4 years progressive experience in clinical operations including project coordination, site management and monitoring with some project management experience or equivalent.

University degree, preferably in a scientific discipline

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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