Associate Director, Medical Affairs

Indivior

1d•Remote

About The Position

Indivior is a global pharmaceutical company working to help change patients' lives by developing medicines to treat opioid use disorder (OUD). Our vision is that all patients around the world will have access to evidence-based treatment for the chronic conditions and co-occurring disorders of OUD. Indivior is dedicated to transforming OUD from a global human crisis to a recognized and treated chronic disease. Building on its global portfolio of OUD treatments, Indivior has a pipeline of product candidates designed to expand on its heritage in this category. Headquartered in the United States in Richmond, VA, Indivior employs over 1,000 individuals globally and its portfolio of products is available in over 30 countries worldwide. The Field Medical Advisor serves as a scientific expert and strategic partner within the Medical Affairs team, responsible for engaging with key opinion leaders (KOLs) and key decision makers (KDMs), disseminating critical clinical/HEOR data, and providing accurate, balanced medical information. The Field Medical Advisor provides medical support to external stakeholders within the health ecosystem including office-based treatment providers, health systems, criminal justice, as well as formulary decision makers. The Field Medical Advisor also plays a pivotal role in supporting internal stakeholders through scientific training and field insights, ensuring alignment with the company’s medical and commercial objectives. The ideal candidate is a self-starter who thrives in an autonomous, field-based environment and is capable of independently managing scientific engagements and cross-functional collaboration.

Requirements

Advanced degree required (PharmD, PhD, NP, PA or MD).
2-5 years of experience in a Medical Affairs, MSL or Outcomes/HEOR specialist role (or equivalent) with the pharmaceutical, biotech, or medical device industry.
Must be able to travel by air and vehicle (valid US driver’s license and clean driving record) up to 70% of time.
Must be able and willing to work occasional weekends and evenings.
Infrequent but potential international travel.
Deep understanding of clinical research, regulatory guidelines, and therapeutic area landscape.
Proven ability to engage and influence KOLs and communicate scientific data effectively.
Strong presentation, interpersonal, and project management skills.
Demonstrated ability to work independently in a field-based role, managing time, priorities, and stakeholder relationships with minimal supervision.
Demonstrated ability to collaborate with commercial account teams and deliver scientific value that supports access, formulary inclusion, and health system partnership goals.
Proven ability to work effectively with Medical Affairs, Market Access, Regulatory, and Commercial teams.
Experience leading cross-functional project teams.
Demonstrated strategic thinking.
Unquestionable ethics and integrity with the willingness to stand firm on these principles even under significant pressure.
Know what policies apply to your role and function and adhere to them.
Speak Up: If you see something, say something.

Nice To Haves

BCMAS preferred
Clinical experience or academic background in addiction medicine
Managed care or client management experience

Responsibilities

Identify, develop, and maintain strong relationships with KOLs and healthcare professionals (HCPs) in assigned therapeutic areas.
Facilitate scientific discussions and respond to unsolicited medical inquiries with accurate, evidence-based information.
Serve as a trusted scientific resource at advisory boards, congresses, and investigator meetings.
Serve as a subject matter expert in opioid use disorder (OUD).
Educate HCPs on the neurobiology of addiction, treatment guidelines, and medications for OUD.
Communicate complex clinical and scientific data in a clear, concise, and compliant manner.
Present new research findings, product updates, and therapeutic insights to external stakeholders.
Contribute to the development of scientific materials.
Provide tailored clinical and real-world evidence to inform decision-making within integrated delivery networks (IDNs), accountable care organizations (ACOs), and other health system stakeholders.
Compliantly partner with commercial teams to provide scientific training.
Deliver therapeutic area and product-specific education to field sales teams.
Share field insights and trends with cross-functional teams to inform strategy and development.
Ensure all activities are conducted in accordance with regulatory, legal, and ethical standards.
Maintain accurate documentation of interactions and insights in CRM systems.

Benefits

3 weeks’ vacation plus floating holidays and sick leave
401(k) and Profit Sharing Plan- Company match of 75% on your first 6% of contributions and profit sharing contribution equal to 4% of your eligible pay
U.S. Employee Stock Purchase Plan- 15% Discount
Comprehensive Medical, Dental, Vision, Life and Disability coverage
Health, Dependent Care and Limited Purpose Flex Spending and HSA options
Adoption assistance
Tuition reimbursement
Concierge/personal assistance services
Voluntary benefits including Legal, Pet Insurance and Critical Illness coverage
Gym, fitness facility and cell phone discounts