UK Clinical Project Manager

ICON; United Kingdom; Remote; GBP 60,000 - 80,000; Full time

Job summary

An established industry player is seeking an Oncology Clinical Project Manager to oversee clinical trials in a dynamic and innovative environment. This role offers the opportunity to work closely with a global pharmaceutical leader, focusing on cancer and other critical therapeutic areas. You will be responsible for site management, ensuring compliance and quality in trial execution while leading diverse teams. If you're passionate about making a difference in healthcare and have a strong background in Oncology project management, this position is perfect for you. Join a company that values inclusion and empowers its employees to reach their full potential.

Qualifications

• 4+ years in clinical operations with project coordination and site management experience.
• Proven track record in managing Oncology clinical trials.

Responsibilities

• Manage site qualifications, setup, monitoring, and closure of clinical trials.
• Lead Local Study Teams and ensure timely delivery of quality data.

Skills

Oncology Project Management

Clinical Research Monitoring

Client Relationship Management

Team Management

Education

Degree in Life Sciences

University Degree in Scientific Discipline

Job description

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.

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.
• Have the overall responsibility for the study commitments within the country and for timely delivery of data to required quality.
• Lead and optimise the performance of the Local Study Teams at country level.
• Liaise with Senior Management in developing study strategy.

Ideal candidates will be those with Oncology project management experience in the clinical space, with a significant background in clinical research monitoring roles; 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.