Neurocrine Biosciences Inc. Posted August 26, 2026

Associate Medical Affairs Director

US CA San Diego, United States Full time
Medical Affairs Director
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Neurocrine Biosciences Inc. 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

Who We Are:

Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit  neurocrine.com , and follow the company on  LinkedIn ,  X , Facebook and YouTube . ( *in collaboration with AbbVie )

About the Role:

Responsible for the development of medical affairs strategy, planning, and tactical implementation for all medical affairs functions including publication planning, data generation and communication, KOL interactions, knowledge management, medical education, advisory boards, and cross-functional partnership. _

Your Contributions (include, but are not limited to):

Medical Affairs Planning

Partner with key cross-functional stakeholders to develop strategic and aligned Medical Affairs Plans for therapeutic areas of interest

Assists in communication and represents plans within the organization. Continuously update plans and inform stakeholders of progress

Collaboratively develop a fully referenced scientific platform and lexicon supporting the foundational understanding of Neurocrine therapeutic platforms, describing their derivation, MOA, multimodal attributes and potential for treating various disorders with unmet medical need

Assist in gaining the endorsement of the platform from internal and external opinion leaders and educate the organization on its content and use

Data Generation

Aid in establishing strategically aligned key areas of interest for IIS, collaborative research agreements and Phase IV clinical trials

Direct and design collaborative research and Phase IV clinical trials for assigned area

May serve on review committees for review and approval of investigator initiated and medical education grant requests

Provide medical input into clinical development and lifecycle management activities

Collaborate with Clinical Development to support clinical trials and pipeline programs

Data Communication

Develop and execute strategically aligned publication plans for key therapeutic areas in collaboration with Medical Communications

Participate in congress planning including medical education, competitive intelligence

Establish working relationships with KOLs and payers to understand the therapeutic landscape, data gaps and areas of educational unmet needs and garner feedback on key programs

Scientific and Medical Consultant to Internal Stakeholders, may be asked to consult External Stakeholders

Serve as Medical/Scientific Subject Matter Expert

Provide knowledge and expertise for assigned products including (but not limited to) PRC, health outcomes plans, MSL activities, speaker programs, training, CME grant reviews or other internal key business processes

Requirements:

PhD AND 7+ years of experience with a combination of clinical practice experience and Medical Affairs or related pharmaceutical consulting capacity. OR

PharmD AND 7+ years of experience with a combination of clinical practice experience and Medical Affairs or related pharmaceutical consulting capacity. OR

MD preferred AND 2+ years of relevant experience Preferred experience: Clinical Practice experience in Psychiatry, Neurology or Movement Disorders

Recognized as an internal thought leader with extensive technical and business expertise within a strategic organization

Applies in-depth knowledge of own function, business / commercial / scientific expertise to solve critical issues successfully and innovatively

Evaluates key business / scientific challenges and completes complex, ambiguous initiatives having cross-functional impact

Strong interpersonal and communication skills as well as strong organizational and team leadership skills are required

Able to work independently and prioritize multiple tasks and goals to ensure the timely, on-target and within-budget accomplishment

Effective communicator with good team collaboration skills. Passion for education and addressing unmet medical needs in Psychiatry or Neurology or related area

Strong knowledge in one of the relevant specialty areas preferred: Neurology, Movement Disorders, Psychiatry or other related field

Comprehensive knowledge of Good Clinical Practices (GCP), ICH, ICJME Guidelines, FDA and other international regulatory body requirements

Experience in proactively engaging internal and external leaders while serving as the medical affairs representative for assigned programs

Understands the connection of clinical, medical, and business needs

Knowledge of aligning business and scientific goals and objectives

Working knowledge of budget development

Proven project management, and problem-solving skills

Analytical, problem-solving, and decision-making skills oriented toward quality work and consistent attention to detail

Strong writing abilities in the scientific or medical field

Uses professional concepts in developing resolution to critical issues and broad design matters

Expertise in developing policies and processes

#LI-SA1

Neurocrine Biosciences is an EEO/Disability/Vets employer.

We are committed to building a workplace of belonging, respect, and empowerment , and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don’t line up to exactly what we have outlined in the job description.

_

The annual base salary we reasonably expect to pay is $173,600.00-$237,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 30% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.

Job details

Seniority
Director
Function
Medical Affairs
Therapeutic area
Not listed
Location
US CA San Diego, United States
Employment type
Full time

How this role compares

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

We currently track 256 comparable Director Medical Affairs roles across 50 biopharma companies.

256Comparable roles tracked
238Currently active
50Companies hiring similar roles
19Countries represented

Salary context

136 of 256 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 $173,600/yr – $237,000/yr
Lowest disclosed · Principal Strategic Medical Writer · AbbVie $109,500/yr – $208,500/yr
Highest disclosed · Sr Medical Director (Heme Oncology) (Boston, US) · Servier $298/hr – $350/hr (≈ $619,840–$728,000/yr)
Peer group range $159,000 – $673,920 (median $264,000)

Where these roles are based

Top locations among the 256 comparable roles

United States196
United Kingdom14
China's Mainland8
Switzerland6
Japan6
Spain4

+ 13 more countries

Seniority mix

256 of 256 peers have a known seniority level

Director226
Senior Director23
Principal7

Therapeutic area mix

123 of 256 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology60
Neuroscience14
Immunology14
Respiratory11
Cardiovascular / CVRM8
Rare Disease8
Dermatology & Aesthetics4
Vaccines & Infectious Disease2
Gastroenterology1
Ophthalmology1

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Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

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.

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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.