Novartis Posted August 6, 2026

Clinical Research Medical Advisor (CRMA)

Amsterdam, Netherlands Regular
Medical Affairs Associate

Novartis is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

WORK ARRANGEMENT: Hybrid, #LI-Hybrid LOCATION: Amsterdam, Netherlands RELOCATION SUPPORT: This role is based in Amsterdam, Netherlands. Novartis is unable to offer relocation support: please only apply if accessible. What if your expertise could help accelerate the development of life-changing medicines for patients around the world? As a Clinical Research Medical Advisor, you will play a pivotal role in bringing innovative therapies closer to patients by shaping clinical trial strategy, driving operational excellence, and partnering with leading investigators and healthcare experts. This is a unique opportunity to combine scientific expertise with cross-functional leadership, influencing the successful delivery of clinical development programs while helping Novartis reimagine medicine for people everywhere.

As a CRMA, you will provide Clinical Development and indication expertise specific to Country/Cluster, and together with the clinical trial operations team, drives the execution of clinical trials with high quality and within planned timelines.Key Responsibilities Validates study designs, is accountable for, and makes the final decision on the clinical/medical trial and program feasibility of implementing a clinical trial protocol based on medical/clinical practice and analysis of the competitive environment in the country.Actively contributes to scientific/clinical/medical aspects of the start-up phase to ensure fast clinical trial site start-up.Provides clinical/medical expertise to clinical trial operations team members and clinical trial sites for Institutional Review Boards (IRB)/ Ethics Committee (EC) interactions.Decides on site/Country-specific scientific/clinical/medical content of the Informed Consent Form (ICF) as needed and ensures appropriateness of patient suitable language.Provides scientific/clinical/medical expertise during interactions with Country/Cluster external Experts (e.g., Regulatory Authorities, Medical Experts, Advisory Boards, Patient Advocacy Groups, etc.).Drives patient recruitment strategies and proactively address enrolment and data quality challenges. Collaborate across functions to deliver high-quality clinical trials on schedule and in compliance. Essential Requirements Advanced scientific degree in Medicine, Pharmacy, or Life Sciences and ideally, 3 years of clinical development experience in the pharmaceutical industry or clinical practiceAbility to manage a study from a scientific/medical/clinical perspective, and a demonstrated capability to problem solve and mediate complex scientific/clinical/medical/operational issues.Ability to lead effectively by communicating well, motivating a cross functional team, and handling and delegating responsibilities.Ability to evaluate protocol feasibility and solve complex clinical challenges. Sound understanding of the overall clinical development process,and International Conference on Harmonization (ICH)/ Good Clinical Practice (GCP) principlesExcellent communication skills with experience influencing cross-functional stakeholders. Fluency in Dutch & English are essential.Demonstrate an agile mindset by setting clear priorities, collaborating openly, and using feedback to make step-by-step improvements – reflecting the core elements of Agile culture within the Dutch organization.Rewards At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and a minimum of 14 weeks paid parental leave. Expected Annual Base Salary Range for role: EUR 62,200 – 115,400.The salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.  In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. Further details will be provided during the application process.  Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. Read our brochure to learn more about our global total rewards offering: https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf  Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.  Commitment to Diversity and Inclusion / EEO paragraph: Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-cultureBenefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.Read our handbook (PDF 30 MB)

Job details

Seniority
Associate
Function
Medical Affairs
Therapeutic area
Not listed
Location
Amsterdam, Netherlands
Employment type
Regular

How this role compares

Computed from every other active Medical Affairs role in our database, not just this employer's listings.

We currently track 181 comparable Associate Medical Affairs roles across 64 biopharma companies.

181Comparable roles tracked
145Currently active
64Companies hiring similar roles
37Countries represented

Salary context

13 of 181 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Sr. Manager PSL&D Business Operations Lead · Pfizer $116,000/yr – $193,400/yr
Peer group range $154,700 – $198,000 (median $169,300)

Where these roles are based

Top locations among the 181 comparable roles

Japan24
Germany22
India20
China19
United States15
China's Mainland12

+ 31 more countries

Seniority mix

181 of 181 peers have a known seniority level

Manager125
Associate54
Intern/Fellow/Postdoc2

Therapeutic area mix

56 of 181 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology24
Immunology12
Cardiovascular / CVRM5
Dermatology & Aesthetics4
Vaccines & Infectious Disease4
Neuroscience3
Gastroenterology2
Rare Disease1
Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
GlaxoSmithKline B.V. Amersfoort, Netherlands Associate
Same function Same seniority Same country
50%similar
Gilead Sciences Netherlands BV Amsterdam, Netherlands Manager
Same function Adjacent seniority Same country
45%similar
AbbVie Seoul, Seoul Associate
Same function Same seniority
45%similar
AbbVie Seoul, Seoul Associate
Same function Same seniority
45%similar
AbbVie Seoul, Seoul Associate
Same function Same seniority
45%similar
AbbVie Bengaluru, KA Associate
Same function Same seniority

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Scientifc Advisor - Specialty
GlaxoSmithKline B.V. · Amersfoort, Netherlands · Associate
Function Therapeutic area Seniority Country
45%
Medical Advisor, Gastro
AbbVie · Seoul, Seoul · Associate
Function Therapeutic area Seniority Country
45%
Medical Advisor Allergan Aesthetics
AbbVie · Hod Hasharon, Center District · Associate
Function Therapeutic area Seniority Country
45%
Medical Advisor--IMMU
Novartis · Shanghai (Shanghai), China · Associate
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.