Syneos Health Commercial Solutions
Medical Science Liaison
Syneos Health Commercial Solutions, Boston, Massachusetts, United States, 02298
Position Overview
The Medical Science Liaison (MSL) is a field‑based scientific and clinical expert that strategically supports the medical and scientific objectives of Syneos Health. The role focuses on engagement with clinical study sites, investigators, and study personnel to facilitate rapid study start‑up, patient identification, and enrollment efforts.
The MSL is responsible for communicating and educating healthcare practitioners on the science and clinical application of RNAi therapies, acting as a regional medical and scientific resource. The MSL builds relationships with internal stakeholders, CRO partners, investigators, and key opinion leaders while ensuring full compliance with company policies and regulatory requirements.
Key Responsibilities
Act as a strategic liaison between clinical investigators, internal stakeholders, and CRO partners to ensure timely communication, site support, and high‑quality study execution.
Collaborate with Clinical Development, Clinical Operations, and CROs on site identification, evaluation, initiation, and training.
Educate and engage site staff to optimize trial execution, ensure protocol compliance, and meet enrollment timelines.
Lead outreach to referring sites to raise awareness of Phase III hypertension studies, clarify eligibility criteria, and drive patient referrals.
Support and monitor site‑specific patient recruitment strategies; share insights with study management teams.
Participate in Site Initiation Visits, investigator meetings, Steering Committees, and cross‑functional project activities.
Capture and communicate actionable medical insights from the field to inform clinical and medical strategies.
Build and maintain relationships with key opinion leaders in cardiovascular medicine and hypertension for education and potential research collaboration.
Deliver scientific education on investigational therapy mechanisms and emerging clinical data across diverse settings.
Monitor and report regional and site‑level trends, recruitment barriers, and protocol feedback to support operational improvements.
Gather and share competitive intelligence to inform strategic planning.
Represent the company at scientific congresses, providing educational support and summarizing key findings.
Ensure all activities comply with company policies and applicable regulatory standards.
Complete timely and accurate administrative documentation and reports.
Travel:
70% travel, including overnight and weekend travel as needed. Qualifications
Advanced degree in life sciences (PharmD, MD, PhD, DNP, DHSc, or equivalent).
Minimum 3+ years of experience in the pharmaceutical or biotech industry, focusing on medical affairs or field medical roles.
Preferred experience supporting Phase II/III clinical trials.
Prior history in hypertension or cardiovascular therapeutic areas.
Proven ability to build and maintain relationships with KOLs and clinical site staff.
Strong communication, presentation, and interpersonal skills.
Excellent written and verbal communication skills.
Ability to collaborate effectively with cross‑functional teams and external stakeholders.
Candidates must reside within the assigned geography.
Syneos Health is an affirmative action/equal opportunity employer (Minorities/Females/Veterans/Disabled).
Syneos Health has a voluntary COVID‑19 vaccination policy.
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The MSL is responsible for communicating and educating healthcare practitioners on the science and clinical application of RNAi therapies, acting as a regional medical and scientific resource. The MSL builds relationships with internal stakeholders, CRO partners, investigators, and key opinion leaders while ensuring full compliance with company policies and regulatory requirements.
Key Responsibilities
Act as a strategic liaison between clinical investigators, internal stakeholders, and CRO partners to ensure timely communication, site support, and high‑quality study execution.
Collaborate with Clinical Development, Clinical Operations, and CROs on site identification, evaluation, initiation, and training.
Educate and engage site staff to optimize trial execution, ensure protocol compliance, and meet enrollment timelines.
Lead outreach to referring sites to raise awareness of Phase III hypertension studies, clarify eligibility criteria, and drive patient referrals.
Support and monitor site‑specific patient recruitment strategies; share insights with study management teams.
Participate in Site Initiation Visits, investigator meetings, Steering Committees, and cross‑functional project activities.
Capture and communicate actionable medical insights from the field to inform clinical and medical strategies.
Build and maintain relationships with key opinion leaders in cardiovascular medicine and hypertension for education and potential research collaboration.
Deliver scientific education on investigational therapy mechanisms and emerging clinical data across diverse settings.
Monitor and report regional and site‑level trends, recruitment barriers, and protocol feedback to support operational improvements.
Gather and share competitive intelligence to inform strategic planning.
Represent the company at scientific congresses, providing educational support and summarizing key findings.
Ensure all activities comply with company policies and applicable regulatory standards.
Complete timely and accurate administrative documentation and reports.
Travel:
70% travel, including overnight and weekend travel as needed. Qualifications
Advanced degree in life sciences (PharmD, MD, PhD, DNP, DHSc, or equivalent).
Minimum 3+ years of experience in the pharmaceutical or biotech industry, focusing on medical affairs or field medical roles.
Preferred experience supporting Phase II/III clinical trials.
Prior history in hypertension or cardiovascular therapeutic areas.
Proven ability to build and maintain relationships with KOLs and clinical site staff.
Strong communication, presentation, and interpersonal skills.
Excellent written and verbal communication skills.
Ability to collaborate effectively with cross‑functional teams and external stakeholders.
Candidates must reside within the assigned geography.
Syneos Health is an affirmative action/equal opportunity employer (Minorities/Females/Veterans/Disabled).
Syneos Health has a voluntary COVID‑19 vaccination policy.
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