Site Engagement Liaison

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

We are seeking experienced Senior CRAs who are ready to advance their careers by stepping into a Site Engagement Liaison role and joining our diverse, dynamic FSP team.

In this role, you will be responsible for the management of clinical Investigators and sites being considered or participating in sponsor's clinical trials.

You will be responsible for site identification and qualification, the timely delivery of clinical trial enrollment in accordance with objectives, timely delivery of database locks, issues management at clinical trial sites, and ensuring inspection readiness at all times for assigned therapeutic areas within a country that enables global program delivery

What you will be doing

• Serve as an effective communication “bridge” between sites, third party vendors and the sponsor

• Provide vendor oversight for site monitoring activities at site/country level

• Establishes and develops strong professional relationships with active/potential clinical investigators to expand/maintain clinical research partnership opportunities

• Work with internal and external teams to remove barriers to trial execution at a site and/or country level

• Cross functional collaboration and partnership to ensure alignment in priorities and deliver the portfolio

• Site identification and qualification, enrollment planning and execution, to database lock and close out

• Investigator management activities

• Responsible for identifying potential opportunities to accelerate trial enrollment

• Responsible for the development and implementation of applicable investigator / site risk plans to ensure delivery of clinical trial enrollment commitments and database lock

• Influence and engage with Regulatory bodies, Ethical Review Boards and other National Authorities to represent the sponsor

• Investigator Engagement in the country Clinical Trial environment(s).

• Engage and influence within Country Pharmaceutical Associations / Affiliated bodies

Your profile

• Bachelor’s degree or equivalent 

• Minimum of 5 years experience in the pharmaceutical industry and/or clinical research and strong working knowledge of Good Clinical Practice

• Travel required (50-75%)

• Fluent in English as well as required language to conduct day-to-day business

• Strong knowledge in country regulatory guidelines/requirements

• Therapeutic expertise and knowledge of the clinical research landscape; ability to acquire and maintain therapeutic expertise to support portfolio needs

• Strong self-management and organizational skills; ability to manage workload, set personal priorities and adjust as needed

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What ICON can offer you:

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values.   We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Are you a current ICON Employee? Please click here to apply

Global contract research organization providing outsourced clinical development services. Headquartered in Dublin, Ireland.

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