Clinical Site Manager

ICON Strategic Solutions; United Kingdom; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading healthcare intelligence and clinical research organization is seeking a Senior CRA based in the UK. This role focuses on developing site engagement strategies and building relationships with clinical sites. Ideal candidates will have significant experience in the pharmaceutical industry and a strong understanding of GCP and ICH guidelines. Join a company committed to improving patient lives through innovative research and enjoy a supportive work environment with comprehensive benefits.

Benefits

Comprehensive total rewards package

Continuous learning and professional development

Employee benefits for family support

Qualifications

• Minimum of 5 years' experience in the Pharmaceutical, Biotechnology, or CRO industry.
• At least three years' experience in monitoring trials within a clinical development environment.

Responsibilities

• Develop and execute the Site Engagement Strategy/Plan.
• Engage with clinical sites to build and maintain relationships.
• Support the clinical team in coordinating site engagement activities.

Skills

Problem Solving

Relationship Building

Education

BS or MSc in a life sciences or related field

Job description

We are recruiting UK-based Senior CRAs who are seeking a developmental role with a strong ability to build relationships at site, involving problem solving and data review.

You will partner with a pharmaceutical company committed to improving the lives of those with severe neurological and immunological conditions. This role offers both professional challenge and support, allowing you to make a meaningful impact.

Responsibilities:

1. Develop, communicate, and execute the Site Engagement Strategy/Plan in collaboration with the Sponsor's Clinical Team and key internal stakeholders throughout the study lifecycle.
2. Engage with clinical sites to develop, build, and maintain strong relationships with investigators and staff to ensure high-quality investigative sites supporting the clinical development programs.
3. Support the clinical team in coordinating site engagement activities, understanding the competitive landscape, addressing trial hurdles, and motivating sites to ensure timely trial delivery.
4. Assist with assigned studies from regional and cultural perspectives and support study teams with quality-related visits as needed.
5. Maintain regular communication with the global Site Engagement Team, sharing insights and experiences with internal stakeholders and customers.

Qualifications:

• Minimum of 5 years' experience in the Pharmaceutical, Biotechnology, or CRO industry, preferably with site engagement or investigator-facing roles such as clinical project manager, study coordinator, or clinical research associate.
• BS or MSc in a life sciences or related field preferred. At least three years' experience in monitoring trials within a clinical development environment, preferably in phases 2-4.
• Strong knowledge of GCP and ICH Guidelines, with UK experience.

Why Join?

ICON plc is a global healthcare intelligence and clinical research organization, advancing clinical research from molecule to medicine. We provide outsourced services to pharmaceutical, biotech, medical device, and public health organizations.

Our mission is to accelerate the development of drugs and devices that save lives and improve quality of life, with patients at the center of all we do.

We value our people highly, fostering a culture of continuous learning and professional development. ICON offers a comprehensive and competitive total rewards package, including base pay, variable pay, recognition programs, and employee benefits designed to support you and your family throughout your career.

We are committed to inclusion and diversity, providing an accessible environment free of discrimination and harassment. All qualified applicants will receive equal consideration for employment.