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International Medical Director Jobs in Rutherford, NJ

The New York Times

Director, International Tax

New York, NY · Hybrid

$136K - $172K/yr

About the Role As the International Tax Director you will be a key leader in our international tax ... Benefits may include medical, dental and vision benefits, Flexible Spending Accounts (F.S.A.s), a ...

The New York Times

Director, International Tax

New York, NY · On-site

$180K - $200K/yr

About the Role As the International Tax Director you will be a key leader in our international tax ... Benefits may include medical, dental and vision benefits, Flexible Spending Accounts (F.S.A.s), a ...

WebMD

testing req

Newark, NJ · On-site +1

At least 3 years' experience as a scientific lead or medical director in the medical education ... with international medical experts * Excellent computer skills that include working remotely on ...

Syneoshealth

Sr Medical Scientist

New York, NY · On-site

Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review ... Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good ...

Medelite

Assistant Director of Education

Brooklyn, NY · On-site

$105K - $110K/yr

Assistant Director of Education Assistant Director of Education Reports To: Chief Medical Officer ... IMG and FMG (international medical graduate or foreign medical graduate) * Clinical/ healthcare ...

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International Medical Director information

See Rutherford, NJ salary details

$13.3K

$236.9K

$363.9K

How much do international medical director jobs pay per year?

As of Aug 12, 2026, the average yearly pay for international medical director in Rutherford, NJ is $236,884.00, according to ZipRecruiter salary data. Most workers in this role earn between $201,800.00 and $290,000.00 per year, depending on experience, location, and employer.

What is the difference between International Medical Director vs Medical Affairs Director?

AspectInternational Medical DirectorMedical Affairs Director
Required CredentialsMedical degree, board certification, clinical experienceMedical degree, advanced degree often preferred, clinical background
Work EnvironmentGlobal healthcare companies, multinational pharmaceutical firmsPharmaceutical companies, biotech firms, healthcare organizations
Employer & Industry UsageOverseas markets, international teams, global strategyDomestic and international markets, focus on medical communication and compliance

The International Medical Director typically oversees global medical strategies, requiring extensive clinical and leadership experience, often working across multiple countries. Medical Affairs Directors focus on medical communication, compliance, and supporting product development within specific regions or globally. Both roles require medical credentials but differ mainly in scope and geographic focus.

What is an international medical director?

International Medical Directors are senior healthcare professionals responsible for overseeing medical operations, quality, and compliance across multiple countries or regions. They set clinical standards, develop policies, and ensure that healthcare services align with international regulations and best practices. Their role often involves coordinating multinational teams, managing cross-border healthcare projects, and representing organizations in global medical forums. They also play a key part in strategic planning and risk management for international healthcare delivery.

What are the key skills and qualifications needed to thrive as an international medical director, and why are they important?

To thrive as an International Medical Director, you need a medical degree (MD or equivalent), board certification, and significant leadership experience in clinical settings. Familiarity with global health regulations, electronic medical record systems, and international accreditation standards is typically required. Exceptional cultural competency, strategic communication, and decision-making skills help navigate diverse teams and cross-border healthcare challenges. These skills are crucial to ensure high-quality care, regulatory compliance, and effective leadership in multinational healthcare organizations.

How does an international medical director typically collaborate with cross-functional teams across different countries?

An International Medical Director regularly works with diverse teams, including medical affairs, regulatory, clinical development, and commercial teams spread across various countries. This collaboration often involves coordinating global clinical trials, ensuring compliance with local healthcare regulations, and aligning medical strategies with regional needs. Effective communication skills and cultural sensitivity are crucial, as the role frequently requires virtual meetings, travel, and adapting to different healthcare systems and practices. Building strong relationships with local leaders and understanding regional market dynamics are key to successfully driving global medical initiatives.
International Medical Director jobs near you

Scientific Director / Senior Medical Director, Multiple Myeloma (International Medical Affairs)

AbbVie

Florham Park, NJ • On-site

$182K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 22 days ago

AbbVie rating

8.6

Company rating: 8.6 out of 10

Based on 101 frontline employees who took The Breakroom Quiz

16th of 86 rated pharmaceutical

Job description

Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
The Scientific Director / Senior Medical Director provides specialist medical and scientific input into core strategic and operational medical affairs activities such as: health-care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, scientific communications, and value proposition) and safeguarding patient safety (risk minimization activities and safety surveillance activities). Works closely with sales, marketing, and commercial teams to provide strategic medical input into core brand (product) strategies, and to support medical affairs, marketing activities (promotional material generation and product launches) and market access.
This position is ideally based from our Mettawa, IL or Florham Park, NJ sites but other U.S. sites may be considered. Must follow a hybrid schedule of 3 days/week onsite.
Key Responsibilities:
  1. Initiates medical affairs activities including data generation and dissemination strategy, development of Global Medical Affairs strategy, delivering the Medical Functional Plan, Brand Plan and working with Area and Affiliates to ensure execution of strategy.
  2. Responsible from Medical Affairs for the design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, and Regulatory Submissions and responses.
  3. Has overall responsibility for oversight of the Medical Affairs-led clinical studies, monitoring overall study integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Provides in-house clinical expertise for the molecule and disease, coordinating appropriate scientific activities with internal stakeholders and leadership as they relate to ongoing clinical projects.
  4. M.D.s may participate in design and execution of clinical trial safety; scientifically accountable for resolution of safety issues, safety monitoring, and other scientific reports reported to regulatory authorities. Review and assess all Adverse Events (AE's) and Serious Adverse Events (SAE's).
  5. Acts as a clinical interface and actively solicits opinion through leader interactions related to the molecule and disease area; partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are incorporated into Clinical Development Plans and protocols as appropriate.
  6. Assist in the development of scientifically accurate marketing materials, medical education programs, advisories, and symposia. Assists with the scientific review, development, approval, execution, and communication of affiliate/area/global medical affairs sponsored or supported clinical research activities.
  7. Interact with and coordinates appropriate scientific and medical activities with internal stakeholders (i.e., commercial, market access, HEOR, clinical operations, clinical development, regulatory, etc...) as they relate to on-going medical affairs projects. Serve as the scientific team interface for key regulatory discussions.
  8. Provide scientific/medical education to investigators, clinical monitors, and Global Project Team members related to therapeutic area or disease specific information. Keeps abreast of professional information and technology through conferences and/or medical literature and acts as a therapeutic area resource.
  9. Ensures budgets, timelines, compliance requirements are factored into programs' scientific activities.
  10. Responsible for understanding regulatory requirements related to clinical studies and global drug development and accountable for complying with those requirements.

Qualifications
Experience Requirements
Position will be commensurate with experience.
Scientific Director
  • Advanced Degree PhD or PharmD. Additional post doctorate experience highly preferred.
  • Typically, 10-15 years of experience in the pharmaceutical industry or related.
  • 7-10 years of experience in Medical Affairs with Global Medical Affairs experience highly preferred.

Senior Medical Director
  • Medical Doctorate (M.D.) or equivalent (D.O. or non-US equivalent of M.D.). Relevant therapeutic specialty in an academic or hospital environment preferred. Completion of residency and/or fellowship preferred.
  • Minimum 2 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent. 5 years of experience is preferred.

Qualifications:
  • Substantial understanding of relevant therapeutic area required. Direct subject matter expertise in multiple myeloma highly preferred.
  • Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
  • Proven leadership skills in cross-functional global team environment
  • Ability to interact externally and internally to support global business strategy
  • Must possess excellent oral and written English communication skills

Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this postingbased on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more orless than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paidand may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html

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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013

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