Job Description
Role Summary
• The Medical Science Liaison (MSL) is a therapeutic and disease expert who acts as a science bridge between Company through engages in scientific exchange with medical leaders in the external medical and scientific community. The role provides scientific leaders (SLs) balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products. This work is aligned to these four core pillars: Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights.
• The MSL liaises between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies. The MSL serves as a role model for other field medical team members in ways that include on-boarding and/or sharing of therapeutic expertise.
Responsibilities and Primary Activities
• Is product and disease state expert engaging in non-promotional scientific exchange with SLs or key decision makers (KDMs)
• Provide balanced, accurate, and compliant scientific information on disease areas and Company products upon request.
• Executes Field Medical Engagement Plans within the scope of local and global policies, local rules, and regulations and aligned with the Field Medical standard operating procedure (SOP)
• Is fully versed in the therapeutic area and updated on all major studies, both ongoing and completed; product information on company and other companies’ relevant therapies; clinical data and relevant pipeline data to provide the most accurate data to SLs, KDMS, and the healthcare community, in a balanced way, to improve patient care
• Engages in non-promotional peer-to-peer communication with medical/scientific information to SLs and KDMs on their roster, based on scientific exchange and services oriented toward the stakeholder’s professional interests and needs
• May have the chance to cover multiple countries based on company franchise strategies by:
o Defining and maintaining a roster of SLs and KDMs in their therapeutic area
o Interacting with identified SLs and KDMs by exchanging balanced medical/scientific information and by appropriately communicating these exchanges with internal colleagues
o Utilizing scientific and medical expertise to communicate scientific information in individual and group presentations
• Responds to unsolicited requests for medical, scientific, pipeline, organization product information from SLs or KDMs utilizing appropriate approved scientific materials and appropriately documenting the use of these resources
• Provides insights internally on scientific gaps, ideas, and other topics gathered from scientific exchange to inform areas of interest, clinical trial programs, development programs, and company TA strategy
• Alerts investigators to our company’s investigator-initiated study proposals (MISP) and to the process for submitting investigator-designed proposals for review and approval; encourages and facilitates research publication of MISP studies supported by our company, in strict compliance with global/local guidance regarding MISPs
• Works with GMSA/Global Clinical Trial Operations (GCTO) to identify potential investigators for Phase I, II, and III clinical trials.
• Facilitate Company-sponsored clinical trials and Investigator-Initiated Studies (IIS), ensuring compliance with Vietnamese regulations.
• Support generation of local data (Real-World Evidence) to inform clinical practice and policy.
• Collaborate with investigators on study design, protocol development, and regulatory submissions.
• Ensures that various engagement metrics (both quantitative and qualitative) are achieved
• Provides medical insights and training to internal colleagues, including the organization and competitor products and disease state with their therapeutic knowledge
• Attends/participates in scientific congresses/meetings in local country and internationally to understand the role of emerging data on patient treatment within the TA covered, when requested, allowing for more balanced scientific exchange
• Support for Preparation and execution of non-promotional medical education programs
• Performs all company business in accordance with company policies and procedures and country regulations
Cost Centre Management
• Obtains manager approval for all travel and extraneous expenditures
• Manages cost of local/international travel within the company travel policy
Required Qualifications, Skills, & Experience
• PhD in health or life sciences, PharmD, DNP, MD, or a pharmacy degree. If pharmacy degree, 2+ years of pharmaceutical industry experience
• Minimum 2–3 years in medical affairs, clinical research, or related field; oncology experience preferred.
• Strong scientific knowledge and ability to interpret clinical data.
• Excellent communication and presentation skills.
• Clear and concise communication skills (verbal, written, presentations) and interpersonal skills with the ability to work in cross-functional teams
• Demonstrated analytical skills and a solid understanding of research methodology
• Ability to learn and convey medical/scientific information to healthcare professionals and decision makers
• Knowledge of local pharmaceutical industry guidelines/code, regulatory/reimbursement framework, and clinical research guidelines International Conference on Harmonization – Good Clinical Practice (ICH-GCP), Declaration of Helsinki)
• Adhere to all Company policies, Ministry of Health regulations, and ethical standards in scientific exchange and research activities.
• Ability to travel extensively (up to 70% of the working week)
Required Skills:
Adaptability, Biomedical Sciences, Consultation, Data Analysis, Healthcare Education, Medical Affairs, Medical Communications, Medical Knowledge, Medical Review, Medical Writing, Pharmaceutical Medical Affairs, Professional Guidance, Professional Integrity, Project Management, Promotional Review, Scientific Literature, Strategic Planning, Strategic ThinkingPreferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Not ApplicableShift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
05/31/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.