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ICON plc

Site Engagement Liaison

Posted 7 Days Ago
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In-Office
Chennai, Tamil Nadu, IND
Senior level
In-Office
Chennai, Tamil Nadu, IND
Senior level
Manages clinical trial site engagement and complete site management activities, from pre-trial assessment through closeout. Builds relationships with diverse stakeholders, supports regulatory presentations, ensures compliance with ICH-GCP and trial regulations, and coordinates multiple deliverables. The role requires strong organization, communication, problem-solving, and clinical research or monitoring experience, along with approximately 60% travel.
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Site Engagement Liaison - Mumbai (Hybrid Role)

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.


As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.


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.


Location: Mumbai (Hybrid Role)
Key responsibilities include:

  • 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.


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

ICON plc Chennai, Tamil Nadu, IND Office

200 Feet Radial Rd, MCN Nagar Extension, Chennai, Tamil Nadu, India, 600097

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