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Regional Medical Advisor Onc

0-2 years
Not Disclosed
10 Nov. 7, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title:

Regional Medical Advisor (RMA) – Oncology

Location:

India

Function:

Medical Affairs

Category:

Regional Medical Affairs / Scientific Liaison

Requisition ID:

R372125

Job Posting End Date:

November 20, 2025


About the Role

The Regional Medical Advisor (RMA) acts as a key scientific liaison between the company and healthcare professionals within the assigned region. This role is pivotal in delivering medical and scientific support, building relationships with key opinion leaders, and ensuring the ethical dissemination of medical information in alignment with company strategy and compliance standards.


Key Responsibilities

1. Medical Strategy & Scientific Leadership

  • Identify, engage, and develop relationships with Scientific Leaders (SLs) and Key Decision Makers (KDMs).

  • Build regional, national, and international scientific partnerships to advance understanding of diseases, treatment trends, and practice guidelines.

  • Contribute to the development and implementation of regional medical strategies aligned with business objectives.

2. Scientific Expertise

  • Maintain in-depth, up-to-date knowledge of therapeutic areas, clinical research, and company products.

  • Stay informed on emerging scientific and medical advancements, treatment protocols, and clinical guidelines.

3. Medical Education & Internal Training

  • Provide scientific and medical education to sales, marketing, and cross-functional teams.

  • Develop and deliver training materials, presentations, and scientific symposia.

  • Offer pre-launch and launch training for new products.

4. Scientific Exchange & Communication

  • Facilitate scientific discussions and exchanges with KOLs and healthcare professionals.

  • Present clinical data at conferences, advisory boards, and medical meetings.

  • Ensure accurate, ethical, and compliant communication of scientific data and clinical evidence.

5. Clinical Data & Research Support

  • Interpret and communicate clinical trial data and real-world evidence to relevant stakeholders.

  • Support local studies, including site identification and investigator-initiated trials (IITs).

  • Collaborate with Clinical Development and Regulatory Affairs on trial design and medical input.

6. Cross-Functional Collaboration

  • Work closely with Marketing, Regulatory, Market Access, and Clinical Development teams.

  • Provide scientific guidance for medical communication plans, ethical promotions, and regulatory strategies.

  • Support and lead medical-initiated projects relevant to the Oncology therapeutic area.

7. Medical Information & Support

  • Provide accurate and timely responses to medical inquiries from healthcare professionals.

  • Ensure medical information materials (e.g., FAQs, medical letters) are up to date and compliant.

8. Compliance & Governance

  • Adhere to GCP, ICH guidelines, and company code of conduct.

  • Ensure all external and internal engagements meet regulatory and ethical standards.

  • Promote transparency and compliance in all interactions with external stakeholders.


Qualifications & Experience

Educational Background:

  • Advanced degree in Life Sciences, such as:

    • MD / MBBS / Ph.D. / M.Pharm / MDS / BDS

    • Other degrees in biology, pharmacology, or related fields may also be considered.

Industry Experience:

  • Prior experience in pharmaceutical, biotechnology, or medical device industries is preferred.

  • Experience in medical affairs, clinical research, or scientific communication is advantageous.

Therapeutic Area Expertise:

  • Demonstrated expertise in Oncology (preferred).

  • Familiarity with clinical trials, scientific publications, and patient care within oncology or related areas.


Skills & Competencies

Required Skills:

  • Scientific & Clinical Knowledge (trial design, data interpretation, disease states)

  • Stakeholder Engagement & KOL Relationship Management

  • Medical Writing & Scientific Communication

  • Analytical & Problem-Solving Ability

  • Presentation and Interpersonal Communication Skills

  • Adaptability and Flexibility (field-based environment)

  • Understanding of GCP, ICH, and compliance frameworks

Preferred Skills:

  • Advisory Board Development

  • Healthcare Market Understanding

  • Medical Marketing Strategy & Review

  • Data Analysis and Medical Information Systems

  • Experience in Pharmacovigilance or Drug Safety


Values & Behavioral Expectations

  • Uphold company values of integrity, excellence, and collaboration.

  • Build partnerships internally and externally to support ethical and evidence-based medicine.

  • Demonstrate a commitment to continuous learning and professional growth.


Other Details

Employment Type: Regular
Travel Requirements: Frequent (Field-based)
Work Mode: Field-based / Regional coverage
Relocation: As per business need
Visa Sponsorship: Not applicable


About the Company

Merck & Co., Inc., Rahway, NJ, USA (also known as Merck Sharp & Dohme LLC) is a global leader in healthcare, committed to improving lives through innovative medicines and vaccines. Our Medical Affairs teams bridge science and clinical practice to support informed healthcare decisions.