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Clinical Project Associate Jobs in California (NOW HIRING)

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Clinical Project Associate information

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$12

$31

$54

How much do clinical project associate jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for clinical project associate in California is $31.13, according to ZipRecruiter salary data. Most workers in this role earn between $20.87 and $41.06 per hour, depending on experience, location, and employer.

What is a Clinical Project Associate?

A Clinical Project Associate (CPA) is a professional who supports the planning, execution, and management of clinical trials in the pharmaceutical, biotechnology, or medical device industries. Their responsibilities often include coordinating study documentation, assisting with regulatory submissions, tracking project timelines, and facilitating communication among study teams. CPAs play a crucial role in ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. They work closely with clinical project managers, research associates, and other team members to help bring new therapies and treatments to market.

What are the typical responsibilities of a Clinical Project Associate in supporting clinical trial operations?

As a Clinical Project Associate, you will play a vital role in ensuring the smooth execution of clinical trials by handling administrative and logistical tasks. Your responsibilities often include maintaining study documentation, coordinating meetings, tracking project timelines, and supporting communication between internal teams and external partners such as clinical sites and vendors. You may also assist with regulatory submissions and help monitor compliance with study protocols. This position offers excellent exposure to the clinical research process and can be a stepping stone to more advanced roles within clinical operations.

What are the key skills and qualifications needed to thrive as a Clinical Project Associate, and why are they important?

To thrive as a Clinical Project Associate, you need a background in life sciences or a related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), regulatory documentation, and tools like Microsoft Office is typically required. Excellent communication, teamwork, and time management abilities help professionals excel in supporting project coordination. These skills are crucial for ensuring regulatory compliance, smooth project execution, and effective collaboration within clinical research teams.

What is the difference between Clinical Project Associate vs Clinical Research Coordinator?

AspectClinical Project AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree in health or related field; certifications like CCRP common
Work EnvironmentTypically works with project teams, sponsors, and CROs in clinical trial settingsWorks directly with patients, investigators, and site staff at clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites
Search & Comparison IntentHigh overlap in responsibilities and certificationsSimilar roles but more patient-facing

The Clinical Project Associate primarily supports clinical trial management from a project perspective, working with sponsors and CROs. In contrast, the Clinical Research Coordinator focuses on patient interactions and site management. Both roles require similar educational backgrounds and certifications, but their work environments and daily tasks differ significantly.

What are the most commonly searched types of Clinical Project jobs in California? The most popular types of Clinical Project jobs in California are:
What are popular job titles related to Clinical Project Associate jobs in California? For Clinical Project Associate jobs in California, the most frequently searched job titles are:
What cities in California are hiring for Clinical Project Associate jobs? Cities in California with the most Clinical Project Associate job openings:
Infographic showing various Clinical Project Associate job openings in California as of July 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 2% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $64,745 per year, or $31.1 per hour.
Sr. Director, Clinical Operations

Sr. Director, Clinical Operations

Structure Therapeutics

South San Francisco, CA

$261K - $325K/yr

Other

Medical, Dental, Vision, Retirement, PTO

Re-posted 8 days ago


Job description

About Us:

Structure Therapeutics develops lifechanging medicines for patients using advanced structurebased and computational drug discovery technology. The company's platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs. We are advancing a clinicalstage pipeline of differentiated treatments focused on chronic diseases with high unmet need, including cardiovascular, metabolic, and pulmonary conditions.


Structure Therapeutics is led by an experienced group of international drug innovators and financed by top-tier global life sciences investors. The company completed an initial public offering (IPO) in February 2023. With offices in California and Shanghai, Structure Therapeutics has the benefit of being at the center of life science innovation in both the US and China and capitalizing on the strengths of each geographic location.

Position Summary:

We are seeking a Senior Director, Clinical Operations, who acts as both a strategic leader and a tactical driver. This role is directly responsible for the clinical operations delivery of global clinical trials, requiring proven global clinical operations leadership. The successful candidate must be a leader who can pivot seamlessly from high-level strategic planning to the daily tactical details of operational execution.

The ideal candidate thrives in a fast-paced biotech environment, possessing a proven track record of building high-performing teams while remaining deeply involved in the clinical development lifecycle and vendor oversight.

This position follows a hybrid work model, requiring three days of onsite presence per week at our South San Francisco office.



Essential Duties and Responsibilities:

Strategic Leadership & Oversight

  • Develop and drive clinical trial strategies aligned with corporate goals, while maintaining direct oversight of tactical delivery to ensure timelines and milestones are met.
  • Drive late-stage clinical programs from planning through completion, providing the direct oversight necessary to ensure cost-effective, high-quality delivery
  • Serve as the operational lead for clinical development programs, working closely with regulatory, medical, biostatistics, and other departments.
  • Demonstrated success in managing global clinical trials across multiple therapeutic areas.


Team Leadership & Development

  • Lead, mentor, and grow a team of clinical trial professionals including Clinical Project Managers, Clinical Research Associates, and other key stakeholders.
  • Promote a culture of accountability, transparency, continuous improvement, and high performance.


Operational Excellence

  • Oversee study start-up, site identification, patient recruitment, data collection, and monitoring processes.
  • Ensure compliance with SOPs, ICH/GCP, and relevant regulatory requirements across all clinical activities.
  • Develop, manage, and track clinical trial budgets, timelines, and resource allocation.
  • Demonstrated understanding of pharmaceutical regulatory requirements and impact on development of clinical trials.


Vendor & CRO Management

  • Select, contract, and manage CROs, central labs, and other third-party vendors.
  • Establish and maintain productive relationships with key external partners to ensure deliverables are met.


Cross-Functional Collaboration

  • Partner closely with Clinical Development, Regulatory Affairs, Quality Assurance, and Data Management teams.
  • Represent clinical operations in leadership meetings and provide regular updates to executive stakeholders.
  • Excellent communication and interpersonal skills with the ability to influence stakeholders at all levels.


Qualifications:

  • BS or advanced degree in life sciences or related field.
  • Prior late-stage global operational leadership is required, and cardio-metabolic experience is highly preferred.
  • Minimum 12+ years of progressive experience in clinical research, with at least 5 years in senior leadership roles.


Travel Required:

  • Up to 20%


Structure Therapeutics Inc. is an Equal-Opportunity Employer.

Structure Therapeutics is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $261,000 - $325,000. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate's geography, qualifications, skills, and experience.


At Structure, base pay is only one part of your total compensation package. The successful candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Structure Therapeutics also offers various benefits offerings, including, but not limited to, medical, dental, and vision insurance, 401k match, unlimited PTO, and a number of paid holidays including winter shutdown.


Notice to Recruiters/Staffing Agencies

Recruiters and staffing agencies should not contact Structure Therapeutics through this page. All recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees.


We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file.


Structure Therapeutics' receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Structure Therapeutics and such organization and will be considered unsolicited and Structure Therapeutics will not be responsible for related fees.


Fraud Alert

To all candidates: your personal information and online safety are a top priority for us. At Structure Therapeutics, direct candidates apply through our official career page atBambooHR.


Recruiters will always contact you using the domain of Structuretx.com. We will never request payments, ask for financial account information or sensitive information like social security numbers. If you are unsure if a message is from Structure Therapeutics, please email human resources.