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New · posted Oct 31

Iambic Therapeutics · Pharmaceuticals

Associate Director, Drug Safety

  • Remote, US
  • Remote
  • Full-time
  • Director
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EmploymentFull-time
LocationRemote, US
DeadlineOpen until filled

The role

We are hiring an Associate Director, Drug Safety to join our Safety team at Iambic Therapeutics. Reporting to the Head of Safety, the Associate Director will oversee outsourced pharmacovigilance activities and contribute to regulatory and safety deliverables. The Associate Director will work collaboratively with Quality, Clinical operations, and Clinical development to set up and execute safety processes. A successful candidate will have flexibility in our dynamic and growing organization. The Associate Director will have responsibilities across all phases of development for our oral small-molecule oncology therapies.

The position may be based in our San Diego headquarters or remote.

What you need

  • Bachelor's degree in nursing or pharmacy; advanced degree such as PharmD, MSN, MPH, or equivalent preferred.

  • At least 10 years of combined experience in pharmacovigilance, drug safety, clinical science, or a related environment with a Bachelor’s degree and 6-8 years with an advanced degree.

  • Related experience across both safety science/surveillance and pharmacovigilance operations preferred.

  • Strong understanding of MedDRA and WHODrug dictionaries.

  • Proficiency in the use of Safety Databases.

  • Excellent interpersonal skills and professionalism.

  • Written and verbal proficiency with ability to communicate clinical topics succinctly and clearly.

  • Ability to train, mentor junior Drug Safety staff, contractors, consultants, and vendor personnel.

  • Knowledge of applicable global pharmacovigilance regulations and guidance, including FDA, EMA, ICH, GCP, and GVP requirements.

  • Oncology phase I to III experience preferred.

What you'll do

Case processing and vendor oversight

  • Provide day-to-day oversight of SAE processing activities performed internally and externally.

  • Coordinate reconciliation of safety information across clinical databases and business partners.

  • Monitor vendor performance through compliance trends and review of operational deliverables. Tracking of actions items, issues, corrective actions.

  • Support implementation, maintenance, and enhancement of safety databases as applicable.

Safety Science Support

  • Contribute to aggregate safety reports, safety sections of clinical, safety and regulatory documents as requested.

  • Coordinate safety data deliverables for aggregate reports, regulatory submissions, and health authority requests.

  • Review individual and aggregate safety data and identify emerging trends.

PV Quality, Compliance & Inspection Readiness

  • Co-author and maintain controlled documents, Safety Management Plans, Safety Data Exchange Agreements, and other documents needed to ensure inspection readiness.

  • Support CAPAs, change controls, audits, and regulatory inspections.

Pay and benefits

$164,000 – $205,000 a year

Employer provided
How this compares
  • Company-paid healthcare

  • Flexible spending accounts

  • Voluntary life insurance

  • 401K matching

  • Uncapped vacation

  • Onsite gym and dining

Two Iambic scientists in Iambic lab coats and safety glasses working with sample tubes at a lab bench

From the posting

About Iambic

ABOUT IAMBIC THERAPEUTICS

Iambic is a clinical-stage life-science and technology company developing novel medicines using its AI-driven discovery and development platform. Based in San Diego and founded in 2020, Iambic has assembled a world-class team that unites pioneering AI experts and experienced drug hunters. The Iambic platform has demonstrated delivery of new drug candidates to human clinical trials with unprecedented speed and across multiple target classes and mechanisms of action. Iambic is advancing a pipeline of potential best-in-class and first-in-class clinical assets, both internally and in partnership, to address urgent unmet patient need. Learn more about the Iambic team, platform, pipeline, and partnerships at iambic.ai.

MISSION & CORE VALUES

Our mission is to deliver better medicines through innovations in AI-based discovery technologies. The culture and work at Iambic Therapeutics are profoundly strengthened by the diversity of our people and our differences in background, culture, national origin, religion, sexual orientation, and life experiences. We are committed to building an inclusive environment where a diverse group of talented humans work together to discover therapeutics and create technologies.

PAY AND BENEFITS

We offer industry leading competitive pay, company paid healthcare, flexible spending accounts, voluntary life insurance, 401K matching, and uncapped vacation to our team. We are in a brand-new state-of-the art facility in beautiful San Diego with an onsite gym, dining, and easy access to great places to live and play.

Iambic company page · 7 open roles

Job intelligence

The context around this role

Live data · October 31, 2026

Salary intelligence

How the pay compares

This role's midpoint is 29% below the US median for Clinical Safety & Pharmacovigilance roles at this level.

This roleEmployer provided

$164,000 to $205,000 a year

Director roles in the US69 roles publishing pay

Middle half $213,500 to $281,000, median $260,000
Annual base pay
Annual base payLowMedianHigh
This role$164,000—$205,000
All US$213,500$260,000$281,000

This role: Iambic Therapeutics's own published range. Comparisons: the base pay employers published on open Clinical Safety & Pharmacovigilance roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Safety & Pharmacovigilance

The general path across 113 open Clinical Safety & Pharmacovigilance roles on Regulatory Jobs, with the titles they carry most. Not Iambic's own promotion track.

  1. Earlier

    Associate & Specialist

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

  2. Earlier

    Senior & Principal

    Often: Senior Safety Scientist · Clinical FSP Quality Manager

    $186K median11 open
  3. One step back

    Manager

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

    $170K median15 open
  4. This role

    Director

    Often: Director · Senior Medical Director

    $260K median70 open
  5. Next step

    VP & Executive

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

    $347K median12 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: 5 linesDocumentation and SOPs: 3 linesRegulatory submissions: 1 lineQuality systems and risk: 1 lineClinical trial conduct: 1 lineCollaboration and leadership: 3 linesGMPDocumentationSubmissionsQuality systemsClinical trialsTeamwork
  • GMP and compliance5
  • Documentation and SOPs3
  • Collaboration and leadership3
  • Regulatory submissions1
  • Quality systems and risk1
  • Clinical trial conduct1

Company hiring pulse

Iambic on Regulatory Jobs

7
Open roles
7
Distinct roles
2
Locations

By discipline

  • Clinical6 86%
  • Regulatory1 14%

By level

  • Director3 43%
  • Manager2 29%
  • Senior & Principal2 29%
See all 7 Iambic roles

More roles at Iambic

All 7 Iambic roles

Similar Clinical Safety & Pharmacovigilance roles elsewhere

Associate Director, Drug Safety at Iambic

Open until filled. $164K–$205K a year, employer provided.

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