Site Engagement Liaison

PERSOL; Mumbai; On-site; INR 1,500,000 - 2,100,000; Full time

Job summary

PERSOL is seeking a Site Engagement Liaison to foster relationships with clinical trial sites and advance site engagement in innovative therapies.

The role emphasizes collaboration across teams, guidance on study protocols, and ensuring regulatory compliance, with substantial travel expected to manage multiple sites effectively.

Qualifications

• Bachelor’s or Master’s degree in life sciences or related field.
• 2+ years in Project Management or Clinical Trial Management in an MNC.
• 8+ years onsite monitoring with 5+ years in an MNC.
• Excellent interpersonal and communication skills; able to build rapports with diverse stakeholders.

Responsibilities

• Build and maintain strong relationships with key stakeholders at clinical trial sites (PI, site coordinators, staff).
• Provide guidance on study protocols, procedures, and regulatory requirements to ensure compliance.
• Identify opportunities to improve site engagement and optimize site performance through regular feedback.
• Collaborate with internal teams to develop and implement site engagement strategies per study/site needs.
• Monitor site performance metrics and report updates to study teams.

Skills

Stakeholder management

Site engagement

Communication skills

Organizational skills

Relationship building

Education

Bachelor’s/Master’s in life sciences

Job description

As a Site Engagement Liaison, 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%)