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Site Engagement Liaison

ICON
0-2 years
Not Disclosed
Bangalore, India
9 May 28, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Site Engagement Liaison

Company

ICON plc – A global healthcare intelligence and clinical research organization focused on advancing clinical development and bringing innovative treatments to patients faster.


Job Details

  • Job Title: Site Engagement Liaison

  • Job Requisition ID: JR150510

  • Employment Type: Full-time

  • Work Mode: Office or Home

  • Location: Bangalore, India


About the Role

ICON is seeking a Site Engagement Liaison (SEL) to strengthen relationships with clinical trial sites and support effective study execution.

In this role, you will act as a key link between clinical trial sites and internal study teams, ensuring strong engagement, compliance, and optimal site performance throughout the clinical trial lifecycle.


Key Responsibilities

1. Site Relationship Management

  • Build and maintain strong relationships with:

    • Principal Investigators (PIs)

    • Site coordinators

    • Clinical research staff

  • Serve as a key point of contact for site-related engagement activities.

2. Site Support & Compliance

  • Provide guidance to site staff on:

    • Study protocols

    • Study procedures

    • Regulatory requirements

  • Ensure adherence to:

    • Study protocols

    • ICH-GCP guidelines

    • Regulatory standards

3. Site Engagement Strategy

  • Identify opportunities to improve site engagement.

  • Collaborate with internal teams to design and implement engagement strategies tailored to site needs.

4. Performance Monitoring

  • Monitor site performance metrics.

  • Track engagement outcomes and operational performance indicators.

  • Provide regular updates to study teams.

5. Cross-functional Collaboration

  • Work closely with internal clinical teams to support study execution.

  • Contribute to improving site efficiency and study delivery outcomes.


Required Qualifications

Education

  • Bachelor’s degree in:

    • Life Sciences, or

    • Related field

Experience

  • Prior experience in:

    • Clinical research

    • Site management

    • Or related field (preferred)

Skills & Competencies

  • Strong interpersonal and communication skills.

  • Ability to build and maintain professional relationships.

  • Strong organizational and multitasking abilities.

  • Good problem-solving and prioritization skills.

  • Knowledge of ICH-GCP and clinical trial regulatory requirements.


Additional Requirements

  • Willingness to travel approximately 60% of the time.


Rewards & Benefits

ICON offers a competitive benefits package, which may include:

  • Competitive salary

  • Health insurance for employees and families

  • Retirement and savings plans

  • Life assurance coverage

  • Employee assistance and wellness programs

  • Flexible benefits (e.g., gym memberships, travel support, childcare options)

  • Paid annual leave

Benefits vary depending on role and location.


Inclusion & Accessibility

ICON is committed to building an inclusive, diverse, and accessible workplace.

All qualified applicants receive equal consideration regardless of race, gender, disability, or background.

Reasonable accommodations are available during the recruitment process upon request.