Medical Director Jobs in Maryland
Medical Director jobs in Maryland are in strong demand, concentrated in health system leadership, managed care, and government health agencies across a market that ranks among the most active on the East Coast. Baltimore, Bethesda, and Rockville are the primary hiring metros, anchored by employers such as Johns Hopkins Medicine, Kaiser Permanente Mid-Atlantic, and CareFirst BlueCross BlueShield. The most in-demand specialties are utilization management, population health, and behavioral health medical direction. Find a role that fits below and apply directly.
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As a Global Development Medical Director with a focus on Cardiovascular/Renal or Metabolic dysfunction (including Diabetes, Obesity and NASH/MASH), you play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. The Global Development Medical Director in Late Phase CVRM (Cardiovascular, Renal, and Metabolic diseases) is responsible for the design, conduct, monitoring, data interpretation and reporting of individual clinical trials ensuring that the clinical data collected within the study will allow determination of the benefits and risks of the compound, as well as allow for the intended label indication and price in markets globally. The individual operates according to the highest ethical standards to align with internal SOPs, local regulations, laws, Good Clinical Practice, and regulatory requirements.
Medical expert accountabilities
- Provide strategic medical and scientific knowledge and support the design, initiation, execution, completion, and interpretation of a clinical study
- Accountable to deliver medical information, answers, and clarifications to Regulators, Ethics Committees, Marketing Companies, Investigators/Sites
Trial conduct and hands-on delivery accountabilities
- Accountable to the Global Clinical Head (GCH) for the medical aspects and design of studies. Also responsible for driving decisions within Study Team (ST) remits together with other ST members and for solving medical issues with the study team
- Oversight of medical and ethical components of studies including patient safety in compliance with GCP
- Deliver all relevant study documents (e.g Protocol, Amendments, Statistical Analysis Plan, Informed Consent Form, Case Report Forms, and Safety and Risk-Based Monitoring Plans)
- Conduct safety surveillance on a study level including the process for Adverse Events (AE)/ Serious AE reporting, the querying of missing/unclear data, the review of blinded safety data, and escalation to the GCH/Global Safety Physician when needed
- Medically accountable for international investigator meetings, and support Marketing Companies in national activities
- Approve, with the GCH, the Clinical Study Report; including preparation and production (Introduction, Results, Discussion)
Messaging and external impact accountabilities
- Maintain a high degree of understanding and awareness of new and emerging medical developments, globally
- Apply strategic intent when working with Alliance partners, Regulatory Authorities, payers, opinion leaders, prescribers and consumers of AstraZeneca products
- Provide guidance for investigator-initiated trials in collaboration with regional marketing companies
Basic Qualifications:
- Graduate of a recognized school of medicine with an M.B.B.S. or M.D. degree with specialty or experience in the Cardiovascular, Renal or Metabolism (including obesity, diabetes, MASH) therapeutic areas,
- 3+ years of pharmaceutical industry experience OR 3+ years of clinical research experience in the academic or clinical practice setting
- Demonstrated partnership and collaboration skills, including acting as the leader and clearly communicating across countries and cultures
- Fluent in oral and written English, with good presentation skills and effective communication
Desired Qualifications:
- Clinical research expertise in relevant therapy area in study design, protocol development, monitoring and implementing clinical trials, interpreting and reporting trial results
- Credibility in scientific and commercial environments
The annual base pay for this position ranges from $241,613 – $362,420 USD. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program. Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility.
Join us in our unique and bold world.
Date Posted
26-Oct-2026Closing Date
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
As a Global Development Medical Director with a focus on Cardiovascular/Renal or Metabolic dysfunction (including Diabetes, Obesity and NASH/MASH), you play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. The Global Development Medical Director in Late Phase CVRM (Cardiovascular, Renal, and Metabolic diseases) is responsible for the design, conduct, monitoring, data interpretation and reporting of individual clinical trials ensuring that the clinical data collected within the study will allow determination of the benefits and risks of the compound, as well as allow for the intended label indication and price in markets globally. The individual operates according to the highest ethical standards to align with internal SOPs, local regulations, laws, Good Clinical Practice, and regulatory requirements.
Medical expert accountabilities
- Provide strategic medical and scientific knowledge and support the design, initiation, execution, completion, and interpretation of a clinical study
- Accountable to deliver medical information, answers, and clarifications to Regulators, Ethics Committees, Marketing Companies, Investigators/Sites
Trial conduct and hands-on delivery accountabilities
- Accountable to the Global Clinical Head (GCH) for the medical aspects and design of studies. Also responsible for driving decisions within Study Team (ST) remits together with other ST members and for solving medical issues with the study team
- Oversight of medical and ethical components of studies including patient safety in compliance with GCP
- Deliver all relevant study documents (e.g Protocol, Amendments, Statistical Analysis Plan, Informed Consent Form, Case Report Forms, and Safety and Risk-Based Monitoring Plans)
- Conduct safety surveillance on a study level including the process for Adverse Events (AE)/ Serious AE reporting, the querying of missing/unclear data, the review of blinded safety data, and escalation to the GCH/Global Safety Physician when needed
- Medically accountable for international investigator meetings, and support Marketing Companies in national activities
- Approve, with the GCH, the Clinical Study Report; including preparation and production (Introduction, Results, Discussion)
Messaging and external impact accountabilities
- Maintain a high degree of understanding and awareness of new and emerging medical developments, globally
- Apply strategic intent when working with Alliance partners, Regulatory Authorities, payers, opinion leaders, prescribers and consumers of AstraZeneca products
- Provide guidance for investigator-initiated trials in collaboration with regional marketing companies
Basic Qualifications:
- Graduate of a recognized school of medicine with an M.B.B.S. or M.D. degree with specialty or experience in the Cardiovascular, Renal or Metabolism (including obesity, diabetes, MASH) therapeutic areas,
- 3+ years of pharmaceutical industry experience OR 3+ years of clinical research experience in the academic or clinical practice setting
- Demonstrated partnership and collaboration skills, including acting as the leader and clearly communicating across countries and cultures
- Fluent in oral and written English, with good presentation skills and effective communication
Desired Qualifications:
- Clinical research expertise in relevant therapy area in study design, protocol development, monitoring and implementing clinical trials, interpreting and reporting trial results
- Credibility in scientific and commercial environments
The annual base pay for this position ranges from $241,613 – $362,420 USD. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program. Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility.
Join us in our unique and bold world.
Date Posted
26-Oct-2026Closing Date
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
See All 51 Medical Director Jobs in Maryland
Find roles in Maryland that match your experience and apply in just a few clicks.
Find Medical Director JobsMedical Director Jobs by City in Maryland
Where Maryland roles are concentrated, by current openings.
Medical Director Job Market in Maryland
A snapshot from current Maryland openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Healthcare & Medical Services
- Insurance
What Maryland Employers Look For
The qualifications that appear most often in medical director jobs across Maryland.
- Active Maryland medical license issued by the Maryland Board of Physicians required
- Board certification in a relevant specialty recognized by ABMS or AOA
- MD or DO degree from an accredited medical school with completed residency training
- Minimum five years of clinical experience in a relevant specialty or care setting
- Demonstrated leadership experience managing clinical teams or quality improvement programs
- Familiarity with Maryland regulatory requirements, COMAR standards, and payer compliance
Medical Director Jobs in Maryland: Frequently Asked Questions
How do you become a medical director in Maryland?
To become a medical director in Maryland, you must hold an active Maryland medical license issued by the Maryland Board of Physicians, which requires an MD or DO degree, completion of an accredited residency, and passage of USMLE or COMLEX exams. Most Maryland employers also require board certification in a relevant specialty and several years of clinical experience before considering candidates for a director-level role.
Which companies hire medical directors in Maryland?
Companies currently hiring medical directors in Maryland include MedStar Health, AstraZeneca, and Centurion Health, per current listings on Migrate Mate as of October 2026. Maryland's concentration of health systems, federal contractors, and regional managed care organizations makes it one of the more diverse markets for medical director roles on the East Coast.
Which Maryland cities have the most medical director jobs?
Baltimore, Frederick, and Gaithersburg have the most medical director openings in Maryland. Baltimore drives the largest share of listings through its major academic medical systems and hospital networks, while Bethesda and Rockville reflect the strong presence of managed care organizations, federal health agencies, and health IT firms concentrated in Montgomery County.
Are there remote medical director jobs in Maryland?
Yes, but they are more selective than in purely desk-based fields, since many medical director roles involve on-site clinical oversight, committee leadership, or facility rounding. About 78% of medical director openings tied to Maryland are remote or hybrid as of October 2026, with utilization management, care management, and population health roles most likely to offer remote or hybrid arrangements.
How can I get hired as a medical director in Maryland with little or no experience?
The most realistic entry path is moving into a physician leadership role such as associate medical director, chief medical officer designee, or medical manager within a large Maryland health system or managed care organization. Johns Hopkins Health System, University of Maryland Medical System, and CareFirst BlueCross BlueShield offer physician leadership development tracks that give clinicians administrative exposure before a full director appointment. Pursuing certification through the American Association for Physician Leadership while still in a clinical role strengthens a Maryland candidacy considerably.
Where can I find and apply to medical director jobs in Maryland?
You can find and apply to medical director jobs in Maryland on Migrate Mate, which lists current Maryland openings from health systems, managed care organizations, and government health contractors across the state. Find roles that fit your specialty and experience level and apply directly to each employer.
See All 51 Medical Director Jobs in Maryland
Find roles in Maryland that match your experience and apply in just a few clicks.
Find Medical Director Jobs