Clinical Site Manager

ICON; United States; Remote; USD 80,000 - 110,000; Full time

Job summary

Join a forward-thinking company as a Senior CRA, where you will play a vital role in enhancing clinical development for neurological and immunological conditions. This position involves building strong relationships with clinical sites, supporting trial delivery, and collaborating with a dedicated clinical team. You will thrive in a challenging yet supportive environment that values continuous learning and professional growth. With a focus on inclusivity and belonging, this role offers a competitive rewards package and the opportunity to make a meaningful impact in advancing healthcare solutions.

Benefits

Comprehensive employee benefits

Professional development opportunities

Recognition programs

Variable pay options

Qualifications

• Minimum 5 years in Pharmaceutical, Biotechnology, or CRO industry.
• Experience in monitoring trials in clinical development, preferably phases 2-4.

Responsibilities

• Develop and execute Site Engagement Strategy/Plan with stakeholders.
• Engage with clinical sites to build relationships and ensure quality.

Skills

Site Engagement Strategy

Relationship Building

Problem Solving

Data Review

Knowledge of GCP and ICH Guidelines

Education

BS or MSc. degree in Life Sciences

Job description

We are recruiting UK-based Senior CRAs seeking a developmental role with strong relationship-building skills at the site level, 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 program offers a challenging yet supportive environment to advance your professional career and make a meaningful impact.

Responsibilities:

1. Develop, communicate, and execute 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 client's clinical development.
3. Support clinical team in coordinating and executing site engagement activities, understanding the competitive landscape, addressing trial hurdles, and motivating sites 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, sharing insights and experiences with team members and key stakeholders.

Qualifications:

• Minimum 5 years of 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. degree in a life sciences or related field preferred. At least three years of experience in monitoring trials in 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 leader in healthcare intelligence and clinical research, advancing clinical development from molecule to medicine. We focus on accelerating the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, central to our culture and success. We are committed to continuous learning, professional development, and providing a comprehensive, competitive rewards package, including base pay, variable pay, recognition programs, and employee benefits.

Inclusion and belonging are fundamental to our culture. We are dedicated to providing an inclusive, accessible environment, free of discrimination and harassment, and all qualified applicants will receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

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