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Clinical Development Jobs in California (NOW HIRING)

NewLimit

Head of Clinical Development

South San Francisco, CA · On-site

$96K - $131K/yr

Description NewLimit is recruiting a VP of Clinical Development to plan and execute our first clinical trials. Our most advanced assets restore youthful hepatic metabolism and hold the potential to ...

Ardelyx

Vice President, Clinical Development

Newark, CA · On-site

The Vice President, Clinical Development will initially serve as a highly hands-on individual contributor responsible for advancing ongoing and planned clinical programs, with a particular focus on ...

Ardelyx

Vice President, Clinical Development

Newark, CA · On-site

The Vice President, Clinical Development will initially serve as a highly hands-on individual contributor responsible for advancing ongoing and planned clinical programs, with a particular focus on ...

Ardelyx

Vice President, Clinical Development

Newark, CA · On-site

The Vice President, Clinical Development will initially serve as a highly hands-on individual contributor responsible for advancing ongoing and planned clinical programs, with a particular focus on ...

Travere

Vice President, Clinical Development

San Diego, CA · On-site +1

$95K - $130K/yr

Department: 106750 Clinical Development Location: San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease. At Travere ...

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Showing results 21-40

All JobsClinical Development JobsClinical Development Jobs in California

Clinical Development information

See California salary details

$14

$34

$88

How much do clinical development jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for clinical development in California is $34.16, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $32.50 per hour, depending on experience, location, and employer.

What is the difference between Clinical Development vs Clinical Research Coordinator?

AspectClinical DevelopmentClinical Research Coordinator
Required CredentialsBachelor's degree, often advanced degrees in life sciences or related fields; certifications like CCRP or RACBachelor's degree in health sciences or related field; certifications like CCRP beneficial
Work EnvironmentPharmaceutical or biotech companies, clinical trial teams, R&D departmentsClinical trial sites, hospitals, research centers
Employer & Industry UsageUsed in pharmaceutical, biotech, and medical device industries during drug development phasesUsed in hospitals, research institutions, and clinical trial sites for managing patient studies

While both roles are involved in clinical trials, Clinical Development focuses on designing and managing the overall drug development process, whereas Clinical Research Coordinators handle the day-to-day operations at trial sites, ensuring protocol adherence and patient coordination.

What is clinical development?

Clinical development is the process by which new pharmaceutical drugs, biologics, or medical devices are tested and evaluated in humans to assess their safety and effectiveness. It typically involves a series of phases (Phase I-IV) of clinical trials, starting with small groups of volunteers and expanding to larger patient populations. The goal is to gather the data needed for regulatory approval and to ensure that new treatments provide benefits that outweigh their risks. Clinical development is a critical step in bringing new therapies from the laboratory to patients.

What do you do in clinical development?

A professional in clinical development designs, manages, and oversees clinical trials to evaluate the safety and effectiveness of new medical treatments or drugs. They coordinate with cross-functional teams, ensure compliance with regulatory standards, and analyze data to support product approval processes. Strong project management skills and knowledge of Good Clinical Practice (GCP) are essential in this role.

What does a clinical development specialist do?

A clinical development specialist designs, manages, and oversees clinical trials to evaluate the safety and effectiveness of new medical treatments or devices. They coordinate with research teams, ensure compliance with regulatory requirements, and analyze data to support product approval processes. Strong knowledge of Good Clinical Practice (GCP) and clinical trial management systems is essential for this role.

What are the key skills and qualifications needed to thrive in clinical development?

To thrive in Clinical Development, you need a strong background in life sciences, clinical trial management, and regulatory compliance, often supported by a relevant degree and experience in clinical research. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are typically required. Excellent communication, problem-solving, and leadership skills help professionals coordinate multidisciplinary teams and adapt to evolving study demands. These skills and qualifications ensure the design, execution, and oversight of safe, effective, and compliant clinical trials essential for successful drug development.

What are some common challenges faced in a clinical development role, and how can I prepare for them?

Professionals in Clinical Development often encounter challenges such as managing complex regulatory requirements, coordinating multi-site clinical trials, and ensuring timely patient recruitment. Staying organized, maintaining clear communication with cross-functional teams, and keeping up-to-date with evolving industry guidelines can help you navigate these hurdles. Developing strong project management and problem-solving skills is also essential for success in this dynamic field.

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 Clinical Development jobs in California?

For Clinical Development jobs in California, the most frequently searched job titles are:

What job categories do people searching Clinical Development jobs in California look for?

The top searched job categories for Clinical Development jobs in California are:

What cities in California are hiring for Clinical Development jobs?

Cities in California with the most Clinical Development job openings:

Clinical Development jobs near you
Infographic showing various Clinical Development job openings in California as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $71,059 per year, or $34.2 per hour.

Head of Clinical Development

NewLimit

South San Francisco, CA • On-site

$96K - $131K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 6 days ago

Job description

Company info
NewLimit is a biotechnology company working to radically extend human healthspan. We're developing medicines to treat age-related diseases by reprogramming the epigenome, a new therapeutic mechanism to restore regenerative potential in aged and diseased cells. We leverage functional genomics, pooled perturbation screening, and artificial intelligence systems to unravel the biology of aging and disease using experiments of unprecedented scale.
Description
NewLimit is recruiting a VP of Clinical Development to plan and execute our first clinical trials. Our most advanced assets restore youthful hepatic metabolism and hold the potential to benefit diverse populations with liver disease and metabolic dysfunction. Our early stage programs have similar potential for impact in renal and inflammatory disease indications.
In this role, you will design and orchestrate clinical trials for some of the world's first reprogramming medicines. You will serve as the company's senior clinical scientist and as a member of our executive team.
As part of your role, you will:
  • Lead and orchestrate clinical development activities in collaboration with external partners.
  • Create clinical trial protocols, author and own regulatory submissions, and contribute to regulatory interactions.
  • Solve the inevitable logistical bottlenecks that block progress of our clinical studies.
  • Serve as a member of NewLimit's Executive Team and contribute to budgeting, goal setting, and technical review decisions.
  • Build and run a clinical development team as we approach first-in-human dosing.
Requirements
  • M.D. or equivalent clinical training
  • Experience planning and orchestrating first-in-human trials
  • Experience with both US FDA and ex-US regulatory agencies (e.g. Australian TGA)
  • Deep knowledge of Good Clinical Practices (GCP)
Nice to have
  • Experience in metabolic and liver disease therapeutic areas
  • Experience leading a clinical development team across multiple therapeutic areas
  • Experience developing products in emerging therapeutic modalities (gene therapy, nucleic acid therapies, cell therapy)
  • Experience managing both early (Phase 1/2) and late-stage (Phase 3) clinical trials
Benefits
  • Health, dental, and vision insurance
  • 401(k) with company match
  • Industry-leading paid time off (PTO) -- 20 days/year for all employees + holidays
  • Paid parental leave
  • Meals and snacks on-site

Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. Learn more at: https://www.newlimit.com/careers

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