UK Clinical Project Manager (Biopharma)

ICON; London; Remote; GBP 45,000 - 75,000; Full time

Job summary

An established industry player is seeking a UK Home-Based Clinical Project Manager to oversee clinical trials within a dynamic environment. This role offers the chance to partner with a renowned global pharmaceutical company, focusing on innovative solutions in various therapeutic areas. The ideal candidate will possess a strong background in clinical project management, with a proven ability to lead diverse teams and manage client relationships effectively. This position not only empowers you to contribute significantly to life-saving projects but also fosters a culture of belonging and continuous improvement, making it an exciting opportunity for driven professionals.

Qualifications

• 4+ years in clinical operations with project coordination and monitoring experience.
• Strong client relationship management and team leadership skills.

Responsibilities

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

Skills

Clinical Project Management

Client Relationship Management

Site Management

Team Management

Cultural Diversity Management

Education

Degree in Life Sciences

University Degree in Scientific Discipline

Job description

UK Home-Based (Non-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 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 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:

UK clinical project management experience in the clinical space, with a significant background in CRA/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 Project Management of clinical trials within the Clinical Research industry.
• 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.