Regulatory Jobs
Hero Gradient Background
AstraZeneca's glass-fronted Discovery Centre in Cambridge at dusk
AstraZeneca logo

New · posted Nov 1

AstraZeneca · Pharmaceuticals

Medical Director, Senior Patient Safety Physician

  • Cambridge, MA
  • Hybrid
  • Full-time
  • Director
Save
EmploymentFull-time
DeadlineCloses Dec 15, 2026

What you need

  • Medical Degree (MD, MBBS, or equivalent).
  • Clinical practice experience following medical qualification.
  • Significant experience in Clinical Safety/Pharmacovigilance within the pharmaceutical or biotechnology industry.
  • Strong knowledge of benefit-risk assessment, risk management, signal detection, and global pharmacovigilance regulations.
  • Experience preparing or reviewing global regulatory safety documents and submissions.
  • Proven ability to influence and lead within a matrix environment.

Preferred Qualificationsnice to have

  • Advanced training in Pharmaceutical Medicine or a related discipline.
  • Experience across multiple therapeutic areas and stages of product development.
  • Experience mentoring or leading safety professionals.

What you'll do

Clinical Safety Leadership

  • Lead the clinical safety strategy for assigned products and programs.
  • Drive medical evaluation of safety data and benefit-risk assessments.
  • Provide expert input into risk identification, characterization, and mitigation activities.
  • Influence safety-related decisions within project teams and governance forums.

Safety Surveillance and Risk Management

  • Provide medical oversight of signal detection, safety surveillance, and risk evaluation activities.
  • Lead interpretation of safety data from clinical trials, post-marketing experience, literature, and other relevant sources.
  • Contribute to risk management planning and the development of appropriate risk minimization strategies.
  • Ensure alignment of safety strategy with development and lifecycle objectives.

Regulatory Safety and Governance

  • Lead and review key regulatory safety deliverables, including DSURs, PBRERs, PADERs, safety responses, and other global submissions.
  • Support major regulatory submissions and interactions with health authorities.
  • Present safety assessments and recommendations to governance committees and senior stakeholders.

Cross-Functional Leadership

  • Serve as the Patient Safety representative in clinical project teams.
  • Build effective partnerships across Clinical Development, Regulatory Affairs, Safety Science, Medical Affairs, and other key functions.
  • Support due diligence, licensing, and business development activities when required.
  • Mentor colleagues and contribute to a culture of scientific excellence, collaboration, and continuous improvement.

Pay and benefits

$250,000 – $375,000 a year

Employer provided
How this compares

What Success Looks Like

  • Sound medical judgement and strategic thinking.
  • Strong collaboration and stakeholder management skills.
  • Ability to communicate complex safety information clearly and effectively.
  • Passion for advancing patient safety and delivering medicines responsibly.
  • 401(k) retirement plan

  • Paid vacation and holidays

  • Paid leaves

  • Medical, prescription drug, dental and vision coverage

  • Short-term incentive bonus

  • Equity-based long-term incentive program

Where you'll work

Cambridge, MAHybridOpen in Maps (opens in a new tab)

More jobs in Cambridge, MA

Working conditions

Medical Director, Senior Safety Physician

We are seeking an experienced physician to provide medical leadership for clinical safety and benefit-risk management across the lifecycle of assigned products and development programs. This role is accountable for shaping and executing safety strategy, evaluating emerging safety data, and ensuring the effective communication of safety information to internal and external stakeholders.

Working within a global, cross-functional environment, you will collaborate with experts across Clinical Development, Regulatory Affairs, Epidemiology, Safety Science, Risk Management, and Medical Affairs to protect patient safety and support the successful development and commercialization of innovative medicines.

A group of smiling AstraZeneca colleagues in China chatting around an outdoor table

From the posting

About AstraZeneca

Date Posted

15-Oct-2026

Closing Date

14-Dec-2026

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.

AstraZeneca company page · 33 open roles
Equal opportunity, accessibility and legal noticesAstraZeneca's statements, word for word

The annual base pay (or hourly rate of compensation) for this position ranges from $249,827 - $374,740 USD. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. 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 (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). 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. 

Job intelligence

The context around this role

Live data · November 1, 2026

Salary intelligence

How the pay compares

This role's midpoint is 18% above the US median for Clinical Safety & Pharmacovigilance roles at this level.

This roleEmployer provided

$250,000 to $375,000 a year

Director roles in Massachusetts26 roles publishing pay

Middle half $212,500 to $291,000, median $229,000

Director roles in the US90 roles publishing pay

Middle half $218,875 to $281,000, median $264,000
Annual base pay
Annual base payLowMedianHigh
This role$250,000—$375,000
Massachusetts$212,500$229,000$291,000
All US$218,875$264,000$281,000

This role: AstraZeneca's own published range. Comparisons: the base pay employers published on open Clinical Safety & Pharmacovigilance roles at the same level on Regulatory Jobs, November 1, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Safety & Pharmacovigilance

The general path across 162 open Clinical Safety & Pharmacovigilance roles on Regulatory Jobs, with the titles they carry most. Not AstraZeneca's own promotion track.

  1. Earlier

    Associate & Specialist

    Often: Associate, Pharmacovigilance Operations/Drug Safety · Clinical Safety Coordinator

    $92K median10 open
  2. Earlier

    Senior & Principal

    Often: Senior Safety Scientist · Clinical FSP Quality Manager

    $172K median17 open
  3. One step back

    Manager

    Often: Senior Manager, Clinical Quality Assurance · Clinical FSP Quality Manager

    $166K median30 open
  4. This role

    Director

    Often: Director · Senior Medical Director

    $264K median92 open
  5. Next step

    VP & Executive

    Often: Head of Multiple Myeloma & AML, Oncology · Head of Patient-Facing Quality Assurance

    $347K median13 open

Skills DNA

What this role leans on

How many of the posting's 24 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 1 lineDocumentation and SOPs: 1 lineValidation and qualification: 1 lineRegulatory submissions: 3 linesQuality systems and risk: 4 linesClinical trial conduct: 2 linesCollaboration and leadership: 10 linesGMPDocumentationValidationSubmissionsQuality systemsClinical trialsTeamwork
  • Collaboration and leadership10
  • Quality systems and risk4
  • Regulatory submissions3
  • Clinical trial conduct2
  • GMP and compliance1
  • Documentation and SOPs1
  • Validation and qualification1

Company hiring pulse

AstraZeneca on Regulatory Jobs

33
Open roles
30
Distinct roles
9
Locations

By discipline

  • Quality15 45%
  • Clinical14 42%
  • Regulatory4 12%

By level

  • Director14 42%
  • Associate & Specialist11 33%
  • Senior & Principal5 15%
See all 33 AstraZeneca roles

More roles at AstraZeneca

All 33 AstraZeneca roles

Similar Clinical Safety & Pharmacovigilance roles elsewhere

Medical Director, Senior Patient Safety Physician at AstraZeneca

Applications close December 15. $250K–$375K a year, employer provided.

Job alerts