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Full Time Pharmd Jd Jobs (NOW HIRING)

$17.50 - $22.75/hr

Regular Full-Time Location: USA (non-CU jobs) Categories: Research ICAP at Columbia University, a ... The successful candidate will hold an advanced recognized Pharmacy Degree (PharmD) or relevant ...

Full Time Pharmd Jd information

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$15K

$241.3K

$387K

How much do full time pharmd jd jobs pay per year?

As of Aug 12, 2026, the average yearly pay for full time pharmd jd in the United States is $241,295.00, according to ZipRecruiter salary data. Most workers in this role earn between $200,000.00 and $300,000.00 per year, depending on experience, location, and employer.

What is the difference between Full Time Pharmd Jd vs Pharmacist?

AspectFull Time Pharmd JdPharmacist
Required CredentialsPharmD degree, JD (law degree optional)PharmD degree, licensure as a pharmacist
Work EnvironmentLegal, healthcare, or pharmaceutical settings; often in legal or consulting rolesRetail, hospital, or clinical pharmacy settings
Employer & Industry UsageLaw firms, healthcare organizations, pharmaceutical companiesHospitals, retail chains, clinics

The Full Time Pharmd Jd combines pharmaceutical expertise with legal knowledge, often focusing on healthcare law, policy, or compliance. In contrast, a Pharmacist primarily dispenses medications and provides patient care in healthcare settings. While both roles require a PharmD, the Pharmd Jd adds a legal dimension, making it suitable for those interested in legal aspects of healthcare.

What are the key skills and qualifications needed to thrive as a full time PharmD JD?

To excel as a Full Time PharmD JD, you need a Doctor of Pharmacy (PharmD) and Juris Doctor (JD) degree, with a deep understanding of pharmacy practice, healthcare regulations, and legal frameworks. Familiarity with drug approval processes, compliance software, legal research databases, and state/federal regulatory systems is vital. Exceptional analytical thinking, attention to detail, and strong communication skills distinguish professionals in this dual-role. These competencies are crucial for navigating complex intersections of healthcare law and pharmacy, ensuring legal compliance, and effectively representing clients or organizations.

What unique challenges might I face balancing legal and clinical responsibilities as a full time PharmD JD?

As a Full Time PharmD JD, you'll often navigate complex intersections between pharmacy practice and legal regulations, which can be challenging. You may be called upon to interpret healthcare laws, advise on compliance, and ensure that pharmacy operations meet both clinical standards and legal requirements. This dual responsibility requires strong time management and adaptability, as you might shift between patient care, legal research, and policy development within a single day. Collaboration with interdisciplinary teams—including pharmacists, attorneys, and healthcare administrators—is common, making communication skills essential.

What is a full time PharmD JD?

A Full Time PharmD JD is a professional who holds both a Doctor of Pharmacy (PharmD) and a Juris Doctor (JD) degree and works in a position that utilizes both qualifications on a full-time basis. These individuals are uniquely trained in both pharmacy practice and law, enabling them to work in areas such as pharmaceutical regulation, healthcare compliance, intellectual property, and policy advocacy. They often work for law firms, pharmaceutical companies, government agencies, or academic institutions, helping to navigate legal issues related to pharmaceuticals and healthcare. This dual expertise allows them to play a critical role in ensuring regulatory compliance, managing risk, and shaping healthcare policy.
More about Full Time Pharmd Jd jobs
What cities are hiring for Full Time Pharmd Jd jobs? Cities with the most Full Time Pharmd Jd job openings:
What are the most commonly searched types of Pharmd Jd jobs? The most popular types of Pharmd Jd jobs are:
What states have the most Full Time Pharmd Jd jobs? States with the most job openings for Full Time Pharmd Jd jobs include:
Infographic showing various Full Time Pharmd Jd job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, 7% Part Time, and 3% Contract. Highlights an 80% Physical, 12% Hybrid, and 8% Remote job distribution, with an average salary of $241,295 per year, or $116 per hour.

Associate Director, Commercial Regulatory Affairs

Bristol-Myers Squibb Company

Princeton, NJ • On-site

$173K - $210K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 4 days ago


Bristol Myers Squibb rating

8.2

Company rating: 8.2 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

32nd of 86 rated pharmaceutical


Job description

Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.
Description: The role of Associate Director of US Commercial Regulatory Affairs requires the ability to apply complex scientific and expert regulatory advice and risk assessment for the development of promotional campaigns and materials for an assigned product/therapeutic area in order to help ensure the Company's objectives are met. Individual will ensure materials are consistent with BMS guiding principles, PhRMA guidelines, FTC guidelines, and applicable FDA regulations and guidances.
Responsibilities include:
  • Provides regulatory advice, risk assessment and mitigation strategies to Commercial Teams, Medical Affairs, Public Affairs, Value Access and Payment, and other internal groups, on all promotional materials, including concepts, disease awareness, and institutional campaigns on assigned product/therapeutic area

  • Provides solution oriented and innovative advice to meet the Company's objectives and goals

  • Provide strategic advice for the development of Office Of Prescription Drug Promotion advisory submissions and sub part e submissions

  • Ensure full regulatory compliance of all promotions with approved labeling and /or FDA guidances

  • Ensure regulatory compliance with sub part e and 2253 regulations

  • Lead training for Commercial teams on sub part e, 2253 regulations and FDA regulations on advertising and promotion

  • Ensure monitoring and maintenance of knowledge of the evolving regulatory landscape to provide innovative solutions and advice

  • Pursues and understands unique perspectives inside and outside BMS to provide risk assessment and mitigation strategies

  • Develop and maintain strong working relationships with internal customers, including Commercial, Medical, Public Affairs, Legal and Compliance

  • Integrate compliance considerations into risk assessment by partnering with Legal/Compliance colleagues

  • Provide advice and guidance as appropriate on the development of draft product labeling to ensure commercially viable US labeling upon which future promotion and advertising will be based

  • Provide input on process improvement and BMS guiding principles as needed

  • Engages with colleagues within the department to help support them in their roles and development

  • Provide direct management to individuals depending on assignment

  • Proactively seeks opportunities to learn and develop leadership skills

Qualifications:
  • BS required; advanced degree preferred (MS, PhD, PharmD, JD)

  • Minimum of 3-5 years Regulatory promotional review or related 5 to 8 years pharmaceutical experience (e.g., Medical promotional review)

  • Experience providing risk assessment to interdisciplinary teams on promotional materials and activities for marketed products and strong interest in FDA advertising and promotion regulations including guidance(s)

  • Ability to propose regulatory strategies for advertising and promotion campaigns, disease awareness, and institutional campaigns

  • Proven aptitude to analyze and interpret efficacy and safety data

  • Experience communicating and negotiating with OPDP

  • Organizational skills and ability to pay attention to details. Demonstrated ability to negotiate and influence others to help build team collaboration

  • Excellent verbal, communication, and presentation skills

  • Excellent interpersonal skills, flexibility, adaptable to a changing environment and adeptness to communicate effectively with cross functional teams and with business partners across the company.

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Compensation Overview:
Princeton - NJ - US: $173,350 - $210,058
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
  • Health Coverage: Medical, pharmacy, dental, and vision care.
  • Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
  • Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.

Work-life benefits include:
Paid Time Off
  • US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
  • Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as "Transforming patients' lives through science™ ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
Supporting People with Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Candidate Rights
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
R1604184 : Associate Director, Commercial Regulatory Affairs

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About Bristol-Myers Squibb

Sourced by ZipRecruiter

Bristol-Myers Squibb is a world-renowned global Biopharmaceutical company headquartered in New York, NY, US. Established in 1887, the company has more than 130 years’ worth of history dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. The company operates in the healthcare industry and thrives on providing a range of pharmaceutical products and services for various medical fields, like oncology, cardiovascular diseases, and immunoscience. Notably, Bristol-Myers Squibb is known for its commitment to relentless research and innovative drug development, which has led to breakthroughs like Opdivo, one of the first immunotherapies.

Industry

Scientific research and development services and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

New York, NY, US