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 UK-based Senior Clinical Research Associates to support vital clinical development programs. The role involves developing site engagement strategies, fostering relationships with clinical sites, and ensuring timely trial delivery. Candidates should possess substantial experience in the pharmaceutical or CRO sectors and a strong understanding of regulatory guidelines.

Benefits

Comprehensive rewards package

Continuous employee development

Inclusive and accessible work environment

Qualifications

• Minimum of 5 years of experience in Pharmaceuticals, Biotechnology, or CRO industry.
• Experience in site engagement or investigator-facing roles.
• Strong knowledge of GCP and ICH Guidelines with UK experience.

Responsibilities

• Develop and execute Site Engagement Strategy in collaboration with Sponsors Clinical Team.
• Engage with clinical sites and maintain strong relationships.
• Support the clinical team in coordinating site engagement activities.

Skills

Relationship Building

Problem Solving

Data Review

Education

BS or MSc. degree in life sciences

Job description

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

You will partner with a pharmaceutical company committed to improving the lives of people with severe neurological and immunological conditions. This program offers challenges and support to advance your professional career while making a meaningful impact.

Responsibilities:

1. Develop, communicate, and execute Site Engagement Strategy/Plan in collaboration with the Sponsors Clinical Team and internal stakeholders throughout the project lifecycle.
2. Engage with clinical sites to 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 by understanding the competitive landscape, addressing trial hurdles, and motivating site staff to ensure timely trial delivery.
4. Support assigned studies from regional and cultural perspectives and assist study teams with quality-related visits as needed.
5. Communicate regularly with the global Site Engagement Team and collaborate to share insights and experiences with internal stakeholders.

Qualifications:

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

Why Join?

ICON plc is a leading healthcare intelligence and clinical research organization. We advance clinical research by providing outsourced services to pharmaceutical, biotech, medical device, and public health organizations.

Our patients are at the center of everything we do. We help accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest asset, central to our culture and success. We are committed to continuous employee development and offer a comprehensive, competitive rewards package, including base pay, variable pay, recognition programs, and supportive benefits to support you and your family throughout your career.

At ICON, inclusion and belonging are fundamental. We are dedicated to providing an inclusive, accessible environment free of discrimination and harassment. All qualified applicants will receive equal consideration for employment regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.