Clinical Research Lead (Site Liaison) - Eastern or Central time zone
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 currently seeking a Clinical Trial Enrollment Liaison to join our diverse and dynamic team. As a Clinical Trial Enrollment Liaison at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
What you will be doing
Primary Responsibilities: This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.
Clinical Investigator Management
Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout
Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements
Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas
Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives
Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc
Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct
Clinical Trial Management
Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery
Leverage performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones
Drive inspection readiness as a continuous discipline across sites
Collaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality
Maintain advanced understanding of local treatment paradigms and standard of care to influence strategic country/site selection and protocol localization
Provide oversight and quality assurance for vendor monitoring, escalating risks proactively
Where applicable, lead end-to-end management of Post-Marketing Safety Studies in compliance with local regulations
Business Management and Engagement
Cultivate a portfolio of strategically aligned, high-impact investigators who consistently prioritize sponsor trials
Enable an exceptional investigator experience by being a responsive, knowledgeable, and valued scientific partner
Collaborate cross-functionally (e.g., Medical, Clinical, Study Delivery) to align on trial and site priorities, troubleshooting challenges with urgency and creativity
Conduct data-informed site prospecting and prioritization, contributing to trial competitiveness and regional strategic execution
Maintain scientific fluency and therapeutic expertise to lead meaningful, solutions-focused discussions with site personnel
Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer
Partner closely with field team colleagues to elevate the investigator and site experience, ensuring seamless collaboration and improving enrollment outcomes and Investigator relationships
Country / Regulatory Engagement (where applicable)
Represent Investigator Engagement with regulatory agencies, ethics committees, and national research organizations in countries/territory
Influence the clinical trial ecosystem to improve regulatory agility and operational feasibility
Ensure that local requirements are translated into compliant, efficient trial execution and that sponsor’s internal processes reflect evolving country landscapes
Partner with leadership to identify and align regional initiatives and contribute to enterprise-wide clinical development success
Your profile
Minimum Qualification Requirements:
Bachelor’s degree or equivalent; strong preference for scientific, clinical, or health-related fields
Minimum 5 years of experience in clinical research or pharmaceutical industry with experience directly interacting with or working with HCPs and clinical sites
Minimum 2 years of relevant clinical or therapeutic area experience in Oncology
Other Information/Additional Preferences:
Advanced degree in a scientific or clinical field (PharmD, PhD, MD, or MSc preferred)
Excellent understanding of GCP, clinical development and operations, and trial lifecycle
Demonstrated understanding of the therapeutic landscape and standards of care, with the ability to apply this knowledge to decision making
Proven ability to build credibility and influence HCP community through scientific acumen and relationship strength
Strategic approach with demonstrated success in delivering results in complex, fast-paced environments
Data-driven decision-making skills; ability to interpret and act on performance and operational metrics
Excellent communication, negotiation, and organizational skills
Deep therapeutic area knowledge and familiarity with local clinical research ecosystems
Experience directly influencing clinical site performance and driving enrollment success
Track record of delivering or exceeding performance targets in a collaborative matrix environment
Experience working with regulators or national bodies in support of clinical trial delivery
English fluency and proficiency in local language(s) as needed
Travel Requirements:
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
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.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
