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Director Clinical Development Jobs in California

Erasca

Sr/Exec Director Clinical Development

San Diego, CA · On-site

$265K - $310K/yr

Reporting to the Chief Medical Officer, the Senior or Executive Director, Clinical Development will drive the clinical aspects of late-stage clinical development studies or programs. This person will ...

Erasca

Sr/Exec Director Clinical Development

San Diego, CA · On-site +1

$265K - $310K/yr

Reporting to the Chief Medical Officer, the Senior or Executive Director, Clinical Development will drive the clinical aspects of late-stage clinical development studies or programs. This person will ...

Erasca

Sr/Exec Director Clinical Development

San Diego, CA · On-site

$265K - $310K/yr

Position Summary:   Reporting to the Chief Medical Officer, the Senior or Executive Director, Clinical Development will drive the clinical aspects of late-stage clinical development studies or ...

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All JobsClinical Development JobsDirector Clinical Development JobsDirector Clinical Development Jobs in California

Director Clinical Development information

See California salary details

$49.3K

$125K

$209.2K

How much do director clinical development jobs pay per year?

As of Aug 2, 2026, the average yearly pay for director clinical development in California is $124,981.00, according to ZipRecruiter salary data. Most workers in this role earn between $92,300.00 and $149,500.00 per year, depending on experience, location, and employer.

What does a Director of Clinical Development do?

A Director of Clinical Development oversees the planning, execution, and management of clinical trials to ensure the safety and efficacy of new therapies. They collaborate with cross-functional teams, regulatory agencies, and key stakeholders to design and implement clinical strategies. Their role includes protocol development, trial monitoring, and ensuring compliance with regulatory standards. Additionally, they analyze trial data, manage budgets, and contribute to the overall drug development process.

What are the most common challenges faced by a Director of Clinical Development?

Directors of Clinical Development often navigate challenges such as aligning multiple cross-functional teams, managing complex project timelines, and ensuring compliance with evolving regulatory standards globally. They may also need to address issues related to trial participant recruitment, data integrity, and budget management. Adapting quickly to shifting priorities while maintaining high ethical and scientific standards is crucial. Successful Directors leverage collaboration, proactive problem-solving, and their in-depth industry knowledge to overcome these challenges and deliver impactful clinical results.

What are the key skills and qualifications needed to thrive in the Director Clinical Development position, and why are they important?

A Director Clinical Development typically requires an advanced degree in life sciences or medicine, extensive experience in clinical research, and a strong understanding of regulatory guidelines. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are highly valued. Exceptional leadership, strategic thinking, and effective cross-functional communication set outstanding candidates apart. These competencies ensure clinical programs are executed efficiently, ethically, and in alignment with organizational goals.

What are the most commonly searched types of Clinical Development jobs in California? The most popular types of Clinical Development jobs in California are:
What are popular job titles related to Director Clinical Development jobs in California? For Director Clinical Development jobs in California, the most frequently searched job titles are:
What job categories do people searching Director Clinical Development jobs in California look for? The top searched job categories for Director Clinical Development jobs in California are:
What cities in California are hiring for Director Clinical Development jobs? Cities in California with the most Director Clinical Development job openings:
Director Clinical Development jobs near you
Infographic showing various Director Clinical Development job openings in California as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $124,981 per year, or $60.1 per hour.

Associate Director, Clinical Development

Mirum Pharmaceuticals

Foster City, CA • Hybrid

Other

Posted 25 days ago

Job description

POSITION SUMMARY

The Associate Director, Clinical Development will be responsible for supporting clinical trial related activities for Brelovitug, a key asset in Phase 3, on a cross-functional team of internal and external experts, investigators and government agencies. Activities include but are not limited to drafting key clinical trial and program-level documents, protocol development, support study startup, recruitment, ongoing clinical development management, and closeout as appropriate. Compliance with internal processes, GCP/ICH and regulatory requirements, study and data monitoring, data analysis are required. The Associate Director, Clinical Development operates in collaboration with other functions including internal Safety, Regulatory, Biometrics, and Clinical Operations teams.

JOB FUNCTIONS/RESPONSIBILITIES

  • Responsible for drafting key clinical trial and program-level documents in collaboration with Clinical Operations, Biostats, Medical Writing and the CROs
  • Responsible for clinical aspects of study startup, execution and close-out in close collaboration with Clinical Operations, Data Management and CRO
  • Supports the monitoring of efficacy and safety data received from the clinical trials
  • Supports preparation of clinical summaries for drug applications
  • Supports preparation of scientific/medical questions from regulatory agencies
  • Support the analysis and drafting of clinical trial and scientific publications
  • Supports the planning, conduct and follow-up of external clinical development- or study-related meetings
  • Responsible for clinical aspects of the TMF
  • Support the running and operational aspects of the Clinical Development team including meeting support, inspection readiness and organizational support

QUALIFICATIONS

Education /Experience:

  • Bachelor's Degree and/or advanced degree in a scientific discipline.
  • PhD or PharmD preferred
  • 3+ years of experience in the pharmaceutical industry, including 2+ years in Clinical Development teams.
  • Manage several clinical trials with multidisciplinary trial teams
  • Experience in working with CROs
  • Medical/scientific expertise appropriate to clinical program
  • Demonstrates ability to establish strong scientific partnership with key investigators
  • Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and clinical development process
  • Advanced knowledge of the assigned therapy area is desired, with the capability to interpret, discuss and represent trial or program level data.

Knowledge, Skills and Abilities:

  • Demonstrated accountability for delivery on clinical studies.
  • Demonstrates excellent scientific writing skills.
  • Experience with basic statistical principles and techniques of data analysis, interpretation and clinical relevance.
  • Strong experience in clinical data review and interpretation.
  • Ability to execute in a fast-paced environment.
  • Detail oriented with exceptional organizational skills.
  • Effective communicator with strong verbal and written skills.
  • Ability to identify issues, analyze situations and provide effective solutions.
  • Solid understanding of the clinical development process.

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