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Site Engagement Liaison
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Min. 2 years experience in Project Management or Clinical Trial Management in an MNC. You will contribute to clinical research activities, taking responsibility…

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Site Engagement Liaison

ICON Plc -
Bengaluru, Karnataka

Apply Now

Job details

Full-time

Benefits

Health insurance

Qualifications

Clinical research
Securities & Exchange Commission
Master's degree
Project management
Presentation skills
Bachelor's degree
Clinical trials
Communication skills

Full job description

Site Engagement Liaison

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Site Engagement Liaison at ICON, you will foster relationships with clinical trial sites, enhancing site engagement, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

You will contribute to clinical research activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

Building and maintaining strong relationships with key stakeholders at clinical trial sites, including principal investigators, site coordinators, and research staff.
Providing support and guidance to site staff on study protocols, procedures, and regulatory requirements, ensuring compliance and successful study conduct.
Identifying opportunities to improve site engagement and optimize site performance through regular communication and feedback mechanisms.
Collaborating with internal teams to develop and implement site engagement strategies tailored to the specific needs of each study and site.
Monitoring site performance metrics and providing regular updates to study teams on site engagement activities and outcomes.

Your Profile:

Required qualifications and experience:

Bachelor's/ Master's degree in life sciences or a related field.
Previous experience in clinical research, site management, or a related field preferred. (i.e. right from Pre-Trials Assessment to Close outs)
Min. 2 years experience in Project Management or Clinical Trial Management in an MNC
Min 8+ years in Onsite monitoring experience with 5+ years in MNC
Should be responsible for complete Site Management
Should have SEC (Subject Expert Committee) presentation Skills to Regulatory Authorities (Preferred)
Strong interpersonal and communication skills, with the ability to build rapport and establish effective working relationships with diverse stakeholders.
Excellent organizational and problem-solving skills, with the ability to prioritize and manage multiple tasks simultaneously.
Knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
Willingness to travel as required (approximately 60%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

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

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Apply Now

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