Medical Affairs: A Complete Guide for Healthcare Professionals

Many healthcare professionals want to stay connected to the healthcare industry without the grind of clinical practice. Medical affairs makes that possible.

The gap between science and the market is exactly what Medical Affairs is designed to bridge.

Introduction to Medical Affairs

What is Medical Affairs?

Medical Affairs is vital in the pharmaceutical and life sciences industry, which bridges science, patients, and healthcare professionals.

It ensures that therapies are safe, effective, and ethically promoted, while supporting education, evidence generation, and patient-centric care.

Often intersects with regulatory roles such as medical device regulatory affairs to ensure products are safe, effective, and ethically promoted.

Medical Affairs: History and Evolution

The Medical Science Liaison (MSL) position originated in 1967 at the Upjohn Company. Initially, it was done by the sales reps to respond to doctors’ scientific questions.

In the long run, medical professionals were trained to replace it, and the position shifted to Medical Affairs so that no biased information could be given.

By the 2000s, medical affairs expanded to include evidence generation, scientific publications, medical education, and patient engagement.

As treatment becomes more complicated, medical affairs assist doctors, patients, and other interested parties know about real-world safety, effectiveness, and data.

Medical Affairs has become a strategic pillar of healthcare that helps connect science and society with quality medical knowledge.

Now that we’ve seen how Medical Affairs evolved, let’s look at the core functions professionals perform today.

Source: medicalaffairs(1)

Can a BDS Graduate get a Job as a Medical Affairs Professional?

Yes, a BDS graduate can comfortably get a job as a medical affairs professional, particularly in roles such as medical advisor, clinical research physician, or pharmacovigilance.

Read below to know what roles a BDS graduate can transition into.

Potential Roles for a BDS Graduate in Medical Affairs

Medical Affairs offers BDS graduates multiple career paths to apply their scientific knowledge beyond dentistry. Read below to know more.

  • Medical Advisor: Evaluating clinical data, coordinating medical activities, and advising on healthcare-related aspects.
  • Drug Developer: A BDS graduate can help contribute to the development and formulation of new medicines.
  • Regulatory Affairs Manager: Focuses on ensuring that the medical products and services are regulatory compliant.
  • Pharmacovigilance: Ensures, monitors, and analyses drug safety data to minimise health risks.
  • Medical Writer: Dental graduates can work as medical writers, where they write educational content for the medical and pharmaceutical sectors.
  • Medical Science Liaison: A BDS graduate who serves as a medical science liaison serve as a bridge between pharma and healthcare professionals by sharing scientific insights, engaging KOLs, and supporting research, clinical trials, and medical education.
Roles for a BDS Graduate in Medical Affairs
Roles for a BDS Graduate in Medical Affairs

Transferable Skills a BDS Graduate Brings to Medical Affairs

As a dentist, you already have a strong foundation that aligns with medical affairs roles.

Your background in clinical knowledge, patient communication, and scientific understanding directly transfers to this field.

Skills like interpreting:

  • Research
  • Explaining complex concepts in simple terms, and
  • Building trust with patients naturally translates into engaging with healthcare professionals and Key Opinion Leaders (KOLs).

In addition, your familiarity with clinical practices and evidence-based medicine equips you to support clinical trials, pharmacovigilance, and scientific exchange with credibility.

Career Path for BDS Graduates: Qualifications & Training

To transition into medical affairs, BDS graduates can strengthen their profile with these additional qualifications, certifications, and industry exposures :

  • Postgraduate courses – Clinical Research, Public Health, or Healthcare Management
  • Certifications – Pharmacovigilance, Regulatory Affairs, Medical Writing, Drug Safety
  • Workshops & training – Scientific communication, Evidence-based medicine, Clinical trials
  • Industry exposure – Internships in pharma, research organisations, or CROs
  • Networking – Attending medical conferences, joining professional associations

What are the Key Functions of Medical Affairs Professionals?

Medical affairs professionals play a bridge between the company and the medical community.

The key functions of a medical affairs specialist are:

  • Educating Healthcare Professionals: provide accurate, balanced, and evidence-backed information about products and therapeutic areas.
  • Developing Medical Content: create and review scientific materials, publications, and presentations to ensure accuracy and compliance.

Evidence generation for medical affairs ensures a systematic data collection related to a particular product. Evidence generation goes beyond clinical trials. It includes:

  • Study specific data
  • Patient outcome information
  • Health Economics and Outcomes Research (HEOR)
  • Post-marketing feedback & research

Together, these activities help create a credible and authentic source of information that supports clinical decision-making and scientific communication.

Medical Affairs professionals collaborate with healthcare providers to contextualise real-world data, ensuring that scattered clinical insights are consolidated and available at scale.

This evidence is critical in shaping healthcare policies, treatment guidelines, and market access decisions.

KOL stands for Key Opinion Leader. They are the experts in their respective fields.

  • Building Professional Relationships: The team builds professional relationships with the KOLs, like researchers, healthcare practitioners, and other experts, to gain insights and validate scientific data.
  • Gathering Insights: Collect feedback and insights from the KOLs to structure guidelines and policies.

The medical affairs team ensures that all activities, like the clinical trials, are carried out safely, adhering to the ethical and regulatory compliance standards.

Their role is crucial in safeguarding patient safety during clinical trials and maintaining scientific integrity across every Medical Affairs function.

The role includes:

  • Ensuring clinical trials follow Good Clinical Practice (GCP) and protect patient interests
  • Guaranteeing that all scientific communication is accurate, balanced, and non-promotional
  • Reviewing medical content and publications for ethical and regulatory compliance
  • Overseeing interactions with healthcare professionals and KOLs to ensure transparency and fair practices

By upholding compliance and ethics, Medical Affairs protects patients, builds trust with healthcare professionals, and reinforces the company’s scientific credibility.

Medical Affairs works closely with other departments such as regulatory affairs, pharmacovigilance, and market access.

This includes alignment with medical device regulatory affairs to ensure consistent, accurate, and compliant scientific messaging across all therapeutic and device areas.

  • Incorporating patient perspectives into decision-making
  • They support patient education and advocacy initiatives to improve health literacy and empower patients in their treatment journey
  • In addition, they work to enhance access to therapies by aligning scientific evidence with payer and policy requirements

What are the Key Roles Within Medical Affairs?

The key roles within the medical affairs (MA) can be included in the 5 main categories:

  • Field Facing Opportunities
    • Medical Science Liaison (MSL):
      • An MSL is a specialist with advanced scientific training. Their main role is to maintain relationships with Key Opinion Leaders (KOLs)
      • Medical affairs MSL provides an external stakeholder link, bridging the gap between clinical development and commercial success.
      • They collect credible insights that help product development.

Source: iqvia(2)

  • Scientific Communication & Information Roles
  • Medical Information Specialist (MIS):
    • Pharmaceutical medical information is a broad term for specialists collecting product data for on and off-label use.
    • MIS also collects data and creates fair, medically backed information for patients and healthcare professionals, including publications and product descriptions for the committee.
    • Apart from this, the MIS also answers questions related to a specific drug through verbal telephonic conversation.
    • Attend medical congresses and scientific meetings to enhance knowledge and provide face-to-face scientific exchange.
    • This role is typically for nurses or pharmacists with drug information residency backgrounds.
  • Medical Communications / Publications Manager
    • Their role is to develop manuscripts, abstracts, posters, and presentations.
    • They act as a bridge between the pharmaceutical clients, clinical experts, and medical writers, ensuring all publications are scientifically accurate, compliant with industry standards, and delivered on time.
  • Strategic & Cross-Functional Roles
    • Medical Advisor / Medical Affairs Manager

Below is the difference between a medical advisor and a medical affairs manager.

AspectMedical AdvisorMedical Affairs Manager
Primary FocusProvides scientific expertise and clinical guidance for a product or therapeutic area.Oversees medical activities and ensures alignment of projects with organisational goals.
Scope of WorkEngages with KOLs, supports clinical trials, gathers medical insights, and participates in evidence generation.Manages cross-functional teams, coordinates medical strategy execution, and supervises operational activities.
Decision-MakingAdvises on clinical and scientific matters; supports evidence-based decisions.Makes managerial decisions regarding resources, timelines, and project prioritisation.
Field EngagementOften interacts with healthcare professionals and KOLs for scientific exchange.Mostly office-based; may interact with teams and stakeholders rather than field HCPs.
Strategic RoleFocused on clinical/scientific strategy for therapeutic areas.Focused on operational and tactical implementation of medical strategy.
ReportingTypically reports to the Medical Manager or the Head of Medical Affairs.Typically reports to the Head of Medical Affairs or the Medical Director.
  • HEOR Medical Affairs & RWE Specialists
    • The main goal of health economics and outcomes research (HEOR), real-world data (RWD), and real-world evidence (RWE) specialists is to analyse health data for better outcomes.
    • These specialists are mainly hired in the following sectors:
      • Pharmaceutical and biotech
      • Clinical research organisations
      • Consulting firms
      • Government and public health organisations
  • Compliance & Governance Roles
    • Compliance & Ethics Officer (Medical Affairs): The specialists ensure that the pharma and biotech companies abide by the regulatory standards for all medical affairs activities, such as:
      • Scientific communications
      • Educational materials, and
      • Stakeholder engagements
    • Key responsibilities are:
      • Developing policies
      • Conducting training and audits
      • Monitoring regulatory changes
  • Leadership Roles
    • Medical Affairs Director / Head of Medical Affairs: They oversee the team, budgets, and alignment with patient and organisational goals.
    • Apart from this, they define the overall medical strategy.
Key Roles Within Medical Affairs
Key Roles Within Medical Affairs

Medical Affairs Salary: What Healthcare Professionals Can Expect

The salary of a medical affairs professional depends on the level of experience, role, company size, and geographic location.

The base pay ranges between 6L and 9L per year(3).

The Future Scope of Medical Affairs for HCPs

The future scope of medical affairs for healthcare professionals (HCPs) lies in real-time, authentic access to scientific data and patient-centric solutions.

With advanced technologies and a diversion towards AI, medical affairs will provide HCPs with deeper insights, better education, and support in making informed treatment/medical decisions.

With their scientific and patient-care expertise, clinicians can build rewarding careers in areas such as:

  • Leadership Roles: Becoming a medical Director or Head of medical affairs, shaping strategy, and guiding cross-functional teams.
  • Research & Evidence Generation: Leading real-world evidence studies, post-marketing research, and clinical trial support.
  • Medical Education & Communication: Training healthcare professionals, developing scientific content, and presenting at medical congresses.
  • Strategic & Advisory Roles: Collaborating with regulatory, market access, and commercial teams to align medical insights with business goals.

The Role of the Medical Affairs Professional Society (MAPS)

The Medical Affairs Professional Society (MAPS) is the largest global nonprofit organisation dedicated to advancing the medical affairs function in the life sciences industry. Its role is to:

  • Professional Development: Provide education, training, and resources for medical affairs professionals across pharma, biotech, and device industries.
  • Best Practices & Standards: Develop and share global standards, frameworks, and best practices for the evolving role of medical affairs.
  • Networking & Collaboration: Create a community where medical affairs professionals can connect, share knowledge, and learn from peers and industry leaders.
  • Thought Leadership: Publish position papers, guidelines, and insights that shape the future of medical affairs.
  • Events & Conferences: Organise global and regional conferences, webinars, and workshops to promote learning and innovation.
  • Career Growth: Offer certifications, mentorship, and career resources to help members grow professionally.

What is the Difference Between Medical Affairs and Regulatory Affairs?

Go through the table below to understand the difference between medical and regulatory affairs.

AspectMedical AffairsRegulatory Affairs
Main FocusScientific exchange, evidence generation, patient engagementRegulatory submissions, approvals, compliance
Key RoleBridge between the company and the medical communityA bridge between the company and regulators
ActivitiesKOL engagement, clinical trial support, publications, and educationPreparing dossiers, labelling, and post-market compliance
OutputScientific knowledge & real-world dataLegal approval & compliance with health authorities
GoalImprove patient outcomes & knowledgeEnsure safe, legal market access for products

Success Stories of BDS Professionals in Medical Affairs

At Odigio, we make the impossible possible! Several of our BDS clients have successfully transitioned into a medical affairs role. Their journeys prove that with the right preparation, BDS.

Conclusion

Medical affairs has become the strategic pillar of the life sciences industry.

It offers a rewarding career path for healthcare professionals that blends science, strategy, and patient care without the routine pressures of clinical practice.

The opportunities are vast and growing if you are interested in leadership, research, education, or cross-functional strategy.

As therapies become more complex and technology evolves, Medical Affairs will remain central to advancing science, ensuring compliance, and improving patient lives.

FAQs: Medical Affairs

A medical affairs professional is crucial in bridging the gap between the scientific/clinical world and the business side of healthcare & pharma.

Their focus is on ensuring that a company’s products are backed by accurate, ethical, and credible science while supporting the needs of healthcare professionals (HCPs), patients, and internal teams.

Medical affairs is one of the best career choices if you want to contribute to the healthcare system beyond clinics.

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