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Cro Cra Jobs in California (NOW HIRING)

IQVIA

CRA 1, IQVIA Biotech

San Francisco, CA · On-site

$71K - $145K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of ...

IQVIA

CRA 1, IQVIA Biotech

Carlsbad, CA · On-site

$71K - $145K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of ...

IQVIA

CRA 1, IQVIA Biotech

Carlsbad, CA · On-site

$71K - $145K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of ...

IQVIA

CRA 1, IQVIA Biotech

San Francisco, CA · On-site

$71K - $145K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of ...

Mindlance

Clinical Research Assocoate

San Diego, CA · On-site

The Position The Clinical Research Associate (CRA) provides support to Study Lead(s) in clinical ... Work closely with CRO to plan for execution of study start-up and ongoing study execution ...

IQVIA

CRA 2, Early Clinical Development

Sacramento, CA · On-site

$90K - $150K/yr

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1.5 years of onsite monitoring, and early ... IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of ...

IQVIA, Inc.

CRA 2, Early Clinical Development

Carlsbad, CA · On-site

$90K - $150K/yr

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1.5 years of onsite monitoring, and early ... IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of ...

IQVIA

CRA 2, Early Clinical Development

San Francisco, CA · On-site

$90K - $150K/yr

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1.5 years of onsite monitoring, and early ... IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of ...

IQVIA

CRA 2, Early Clinical Development

Carlsbad, CA

$90K - $150K/yr

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1.5 years of onsite monitoring, and early ... IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of ...

IQVIA

CRA 2, Early Clinical Development

Carlsbad, CA · On-site

$90K - $150K/yr

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1.5 years of onsite monitoring, and early ... IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of ...

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What is a CRO cra?

CRO CRAs, or Clinical Research Associates working for Contract Research Organizations (CROs), are professionals who monitor clinical trials to ensure compliance with regulatory requirements and study protocols. They act as the link between the sponsor of the clinical trial and the sites conducting the research. Their responsibilities include site selection, study initiation, monitoring visits, data verification, and ensuring patient safety. CRO CRAs often work on multiple studies for different sponsors, providing flexibility and exposure to a variety of therapeutic areas.

Is Cro Cra an entry level job?

Cro Cra is typically considered an entry-level position that may require basic skills related to the specific industry or role. It often involves on-the-job training and does not usually require extensive prior experience or advanced certifications.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong knowledge of Good Clinical Practice (GCP) guidelines and certification can improve job prospects, but the level of difficulty varies based on location and individual qualifications.

What are the key skills and qualifications needed to thrive as a CRO (Chief Revenue Officer), and why are they important?

To thrive as a Chief Revenue Officer (CRO), you need a strong background in sales, marketing, business development, and financial management, often supported by a relevant degree and significant leadership experience. Familiarity with CRM platforms (like Salesforce), analytics tools, and revenue management systems is typically required. Outstanding strategic thinking, communication, and cross-functional leadership skills set exceptional CROs apart. These competencies are essential for driving company growth, aligning teams, and optimizing revenue streams in a competitive market.

What are some of the most common challenges faced by a CRO (Conversion Rate Optimization) manager, and how can they be addressed?

A CRO Manager often faces challenges such as aligning optimization strategies with broader business goals, managing stakeholder expectations, and balancing short-term wins with long-term improvements. It's essential to establish clear communication with marketing, product, and development teams to ensure experiments are prioritized effectively. Data-driven decision making, consistent A/B testing, and staying updated on user behavior trends can help overcome these challenges and drive meaningful results.

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Infographic showing various Cro Cra job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 60% In-person, and 40% Remote job distribution.

On-site Clinical Research Associate

Protagonist Therapeutics

Newark, CA • On-site

$125K - $135K/yr

Full-time

Posted 13 days ago

Job description

Onsite Clinical Research Associate
Job Summary
  • Support ongoing trials and/or set-up and manage new trials.
  • Contributions include:
    • study planning and start-up,
    • project, site and vendor management
    • oversight of study site monitoring and performance
    • clinical operations input into the general clinical development of Protagonist compounds.
We are committed to a thriving in-office culture. This role requires being on-site at our office in Newark, CA 4 days a week.
Skills amp; Attributes

Clinical trial experience that includes international Phase 1-2 trials, involving CROs from study set-up through to completion. Experience with Gastrointestinal, hematology and/or orphan drug trials preferred. High level of appreciation and understanding of the feasibility, regulatory and start-up processes, together along with on-site monitoring and site management. Good overall understanding of the major areas within clinical development. Excellent communication and interpersonal skills, along with attention to detail and critical thinking skills. Strong written and spoken English. Ability to collaborate, problem solve and work in a small dynamic organization with minimal supervision, to achieve personal and collective goals.

Experience Required
2+ years as a CRA within Biotech/Pharma or CRO
Education Required
Bachelors Degree
Travel Required
Yes, up to 10%
Core Responsibilities
  • Serves as the internal primary site operations lead, working with the Project Manager and CROs to achieve efficient study set-up and initiation, ongoing data monitoring all the way through successful study execution and site close-out.
  • Oversight of the site feasibility activities leading to site selection, activation and routine monitoring activities to ensure ongoing data integrity and quality.
  • Develops and reviews integrated site plans/timelines and reports weekly progress including risks and mitigations
  • Develops contingency plans for site performance, with regards to recruitment, data quality etc.
  • Helps ensure the trial stays within the contracted site management scope, progress, timelines and budget.
  • Presents site management strategy and status/metrics at project meetings.
  • Monitors and reports on CRO CRA resource utilization, and analyzes expected vs. actual performance
  • Implements and leverages best monitoring practices
  • Experience and proficiency with Good Clinical Practices (cGCP) and compliance with Protagonist SOPs
  • Works closely and effectively with other cross-functional teams to identify best practices and process improvements.
  • Proficiency with MS Office computer software
  • Other duties and assignments as requested for the overall performance of the function and Company.
The base pay range for this position at commencement of employment is expected to be between $125K and $135K / year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.
Protagonist Therapeutics is a discovery through late-stage development biopharmaceutical company. The Company's proprietary peptide technology platform enables de novo discovery of peptide therapeutics. Two novel peptides derived from Protagonist's proprietary discovery platform are at or near commercialization. ICOTYDE™ (icotrokinra) is approved in the U.S. for the treatment of moderate-to-severe plaque psoriasis in adults and pediatric patients 12 years of age and older who weigh at least 40 kg who are candidates for systemic therapy or phototherapy. ICOTYDE is the first and only targeted oral peptide that precisely blocks the Interleukin-23 receptor (IL-23R) licensed to Janssen Biotech, Inc.,a Johnson amp; Johnson company. ICOTYDE was jointly discovered by Protagonist and Johnson amp; Johnson scientists, with Protagonist having primary responsibility for the development of ICOTYDE through Phase 1, and Johnson amp; Johnson assuming responsibility for further development and commercialization. An NDA for rusfertide, a first-in-class hepcidin mimetic peptide that is being co-developed with Takeda Pharmaceuticals pursuant to a worldwide license and collaboration agreement entered in 2024, is under priority review with the FDA. Protagonist holds an option to co-commercialize rusfertide in the U.S. through a 50/50 profit and loss share structure or can opt-out of this structure. The Company also has a number of preclinical stage drug discovery programs addressing clinically and commercially validated targets including an oral IL-17 peptide antagonist, obesity dual and triple agonists, an oral hepcidin functional mimetic, and the recently announced IL-4 and amylin programs.
More information on Protagonist, its pipeline drug candidates, and clinical studies can be found on the Company's website at https://www.protagonist-inc.com.

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