Clinical Trial Liaison

Ladders; United States; Remote; USD 111,000 - 138,000; Full time

Benefits offered by this job

Health coverage

Pension plans

Life insurance

Wellbeing resources

Job summary

The Ladders is seeking a Clinical Trial Liaison to join a leader in the Pharmaceuticals & Biotech space. This role serves as a scientific and strategic partner to investigators and clinical sites across the study lifecycle.

You will drive enrollment performance, strengthen site engagement, and translate protocol requirements into effective site-level action in a highly collaborative research environment. Location: Remote (US).

Qualifications

• Minimum 5 years of experience in clinical research or the pharmaceutical industry with direct interaction with healthcare professionals and clinical sites.
• At least 2 years of relevant clinical or therapeutic area experience in Oncology.
• Advanced degree in a scientific or clinical field; PharmD, PhD, MD, or MSc preferred.

Responsibilities

• Engage with investigators from identification through enrollment and study closeout.
• Act as a scientific ambassador to ensure deep understanding of protocol intent and eligibility requirements.
• Develop and maintain strategic relationships with investigators across trials.
• Co-create tailored recruitment strategies to enhance enrollment.
• Identify opportunities to accelerate patient recruitment and improve site impact.
• Capture insights from sites to optimize study conduct and protocol design.
• Lead site-level strategy and risk planning for predictable enrollment.

Skills

GCP knowledge

Stakeholder engagement

Clinical trial operations

Education

Advanced degree in scientific/clinical field

Job description

For our client, we are seeking a Clinical Trial Liaison to join the team of a leader in the Pharmaceuticals & Biotech space.

This role will serve as a scientific and strategic partner to investigators and clinical sites throughout the study lifecycle. You will help drive enrollment performance, strengthen site engagement, and contribute insights that improve trial conduct and protocol execution in a highly collaborative research environment.

The position requires strong scientific acumen, credibility with healthcare professionals, and the ability to translate protocol requirements into effective site-level action. You will work cross-functionally to support predictable enrollment and advance clinical development goals across oncology studies.

Location: Remote

Compensation: $110,520 – $138,150 annually

Responsibilities

• Engage with investigators from identification through enrollment and study closeout
• Act as a scientific ambassador to ensure deep understanding of protocol intent and eligibility requirements
• Develop and maintain strategic relationships with investigators across trials
• Co-create tailored recruitment strategies to enhance enrollment
• Identify opportunities to accelerate patient recruitment and improve site impact
• Capture insights from sites to optimize study conduct and protocol design
• Lead site-level strategy and risk planning for predictable enrollment

Qualifications

• Minimum 5 years of experience in clinical research or the pharmaceutical industry, with direct interaction with HCPs and clinical sites
• At least 2 years of relevant clinical or therapeutic area experience in Oncology
• Advanced degree in a scientific or clinical field; PharmD, PhD, MD, or MSc preferred
• Strong understanding of GCP, clinical development, operations, and trial lifecycle
• Proven ability to build credibility and influence the HCP community through scientific acumen

Benefits

• Comprehensive health and wellbeing programs including medical, dental, and vision coverage
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programs and wellbeing resources
• Learning and development opportunities through structured training

Our client is an equal opportunity employer.