Regional Site Liaison - West Coast USA - 12 Month Contract, 1.0 FTE

181 2nd Ave, Ste 600 San Mateo, CA 94401 US

Posted: 10/17/2025 2025-10-17 2025-11-17 Employment Type: Contract Job Category: Clinical Development and Operations Job Number: 623251 Is job remote?: Yes Country: United Kingdom

Job Description

Regional Clinical Site Liaison – West Coast USA (12-Month Contract, 1.0 FTE):

Join a pioneering biopharmaceutical company headquartered in Europe with an extensive US presence, boasting fast-track designations and approvals for therapies treating severe Ophthalmic and Neurological diseases. As a Regional Site Liaison, you will play a pivotal role in advancing clinical development efforts across the West Coast, uniquely blending operational oversight of site management activities and direct support to investigational sites to ensure study excellence. This is an exclusive, full-time, 12-month contract opportunity designed for driven professionals seeking to make a meaningful impact in a fast-paced research environment.

In this dynamic role, you will serve as the primary conduit between the sponsor and clinical sites, overseeing site activities, facilitating patient recruitment, and maintaining strong relationships with principal investigators and site staff. Your experience of working on clinical trials within Ophthalmology and Neurology will be essential to navigating complex clinical trials and fostering operational excellence. With this in mind, you’ll contribute to the successful execution of multiple studies, aligning operational strategies with the sponsor’s goals.

Required Skills:

• Proven experience as a Lead CRA or equivalent, with strong CRO operational oversight capabilities.
• Demonstrable experience in Site Engagement or previously acting as a Clinical Site Liaison, representing the Sponsor at the investigational site and supporting with patient recruitment, training of site staff and acting as a PoC for escalation.
• Extensive experience working within Ophthalmology and Neurology clinical trials.
• Excellent communication and stakeholder management skills to liaise effectively with CRO monitors, site staff, KOLs and PIs.
• Demonstrated ability to support site start-up, monitoring, and study logistics.
• Strong organizational skills with an emphasis on operational excellence and study compliance.
• Ability to travel regularly to clinical sites across the West Coast.

Preferred Education and Experience:

• Bachelor’s degree or higher in life sciences, healthcare, or related fields.
• 8+ years of clinical research experience, with a minimum of 3 years in a lead or oversight role.
• Demonstrated success managing multi-site trials in the US West Coast region.

Other Requirements:

• Must be authorized to work in the US, with legal eligibility to work as a 1099 contractor.
• Willingness to travel frequently to site locations.
• Strong commitment to operational excellence and adherence to regulatory standards.

If you are a proactive, detail-oriented clinical operations professional ready to contribute to innovative therapies that improve quality of life, this opportunity is for you. Apply today to become part of a forward-thinking organization focused on groundbreaking research and patient impact.

Equal Opportunity Employer: We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.

Fraud Alert: Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.

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