Clinical Trial Liaison

Meet Life Sciences Ltd.; Waltham (MA); On-site; USD 120,000 - 180,000; Full time

Job summary

Meet Life Sciences Ltd. seeks an experienced Clinical Trial Liaison (CTL) for Phase III oncology programs. The role is field-based and non-promotional, focusing on investigator relationships, enrollment support, and protocol clarity.

You will collaborate with Clinical Development, Medical Affairs, and CRA teams to drive study success. Ideal candidates hold a PharmD/MD/PhD or equivalent, with 8+ years in the pharma/biotech sector and at least 2 years in field-based medical roles, plus strong

Qualifications

• PharmD, PhD, MD or equivalent advanced scientific degree.
• 8+ years of pharmaceutical or biotech industry experience.
• At least 2 years of field-based medical experience.
• Strong understanding of oncology disease states and current scientific landscape.
• Proven experience engaging with KOLs, investigators, and healthcare professionals.
• Excellent scientific communication, presentation, and relationship-building skills.

Responsibilities

• Build and maintain strong relationships with investigators, KOLs, research staff, and referring healthcare professionals.
• Provide balanced, non-promotional education on disease state, study rationale, protocol requirements, eligibility criteria, and study procedures.
• Identify and help address site-specific enrollment, recruitment, referral, and operational barriers.
• Support investigator meetings, site training, enrollment reviews, and other study activities.
• Identify potential academic and community sites with relevant patient populations and clinical trial capabilities.
• Help develop and strengthen patient referral pathways.
• Gather and communicate field insights around patient flow, recruitment challenges, protocol feasibility, site needs, and competing studies.
• Collaborate closely with Clinical Development, Clinical Operations, Medical Affairs, Patient Advocacy, and CRA teams.
• Escalate medical, safety, regulatory, or protocol-related questions to the appropriate Sponsor team.

Education

PharmD, PhD, MD or equivalent advanced scientific degree

8+ years pharma/biotech industry experience

At least 2 years field-based medical experience

Oncology disease state knowledge

KOL/investigator engagement

Scientific communication & relationship-building

Job description

Clinical Trial Liaison (CTL) – Phase III Oncology

We are currently seeking an experienced Clinical Trial Liaison (CTL) to support Phase III oncology clinical development programs.

This is a field-based, non-promotional clinical role focused on strengthening relationships with investigators and research sites, supporting enrollment and retention, improving protocol understanding, and providing valuable insights to the clinical development team.

Key Responsibilities:

• Build and maintain strong relationships with investigators, KOLs, research staff, and referring healthcare professionals.
• Provide balanced, non-promotional education on disease state, study rationale, protocol requirements, eligibility criteria, and study procedures.
• Identify and help address site-specific enrollment, recruitment, referral, and operational barriers.
• Support investigator meetings, site training, enrollment reviews, and other study activities.
• Identify potential academic and community sites with relevant patient populations and clinical trial capabilities.
• Help develop and strengthen patient referral pathways.
• Gather and communicate field insights around patient flow, recruitment challenges, protocol feasibility, site needs, and competing studies.
• Collaborate closely with Clinical Development, Clinical Operations, Medical Affairs, Patient Advocacy, and CRA teams.
• Escalate medical, safety, regulatory, or protocol-related questions to the appropriate Sponsor team.

Requirements:

• PharmD, PhD, MD, or equivalent advanced scientific degree in a life science discipline.
• 8+ years of pharmaceutical or biotech industry experience.
• At least 2 years of field-based medical experience.
• Strong understanding of oncology disease states, treatment paradigms, and the current scientific landscape.
• Proven experience engaging with KOLs, investigators, and healthcare professionals.
• Excellent scientific communication, presentation, and relationship-building skills.
• Strong ability to work independently while collaborating within a cross-functional, matrixed environment.

Preferred:

Experience with investigational oncology products, early-stage biotech, GCP/ICH standards, medical information systems, or CRM platforms.