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Permanent In House Cra Jobs in California (NOW HIRING)

Collaborate with the clinical monitors, in-house CRA during site selection, qualification and initiation process as well as the scheduling of procedures (ensure good case coverage across clinical ...

Collaborate with the clinical monitors, in-house CRA during site selection, qualification and initiation process as well as the scheduling of procedures (ensure good case coverage across clinical ...

Join a permanent, in-house team that prioritizes patient-centered care and clinical excellence. Your Impact * Direct Care: Deliver high-quality treatments following physician-approved plans to ...

Join a permanent, in-house team that prioritizes patient-centered care and clinical excellence. Your Impact * Direct Care: Deliver high-quality treatments following physician-approved plans to ...

S. citizen or lawful permanent resident) residing in the United States, required due to our work with the Defense Industrial Base * 2 or more years of bookkeeping or transactional accounting ...

S. citizen or lawful permanent resident) residing in the United States, required due to our work with the Defense Industrial Base * 2 or more years of bookkeeping or transactional accounting ...

S. citizen or lawful permanent resident) residing in the United States, required due to our work with the Defense Industrial Base * 2 or more years of bookkeeping or transactional accounting ...

There will also be a possibility to transition into a more permanent in house role or remote project based role depending on success in the position and ability to complete the project.

There will also be a possibility to transition into a more permanent in house role or remote project based role depending on success in the position and ability to complete the project.

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Permanent In House Cra information

What jobs can I get after being a CRA?

After working as a Clinical Research Associate (CRA), you can transition into roles such as Clinical Project Manager, Clinical Operations Manager, Regulatory Affairs Specialist, or Medical Monitor. These positions often require experience in trial management, regulatory knowledge, and strong communication skills, and may involve overseeing clinical studies or ensuring compliance with regulations.

What jobs pay $500,000 a year in the US?

In-house contract research associate (CRA) roles typically do not reach $500,000 annually; however, senior-level positions in pharmaceutical or biotech companies, such as director or executive roles, can exceed this salary with bonuses and stock options. High-paying jobs at this level often require extensive experience, advanced degrees, and leadership responsibilities within the industry.

What is the difference between Permanent In House Cra vs Contract Cra?

AspectPermanent In House CraContract Cra
Employment TypeFull-time, ongoing employmentTemporary, project-based
Work EnvironmentIn-house, within a company's clinical research teamExternal, often at a contract research organization or site
CertificationsTypically requires similar certifications (e.g., GCP, ICH)Same certifications as permanent roles, but may vary by project
Industry UsageCommon in pharmaceutical companies and biotech firmsCommon in CROs and clinical trial sites

In summary, a Permanent In House Cra is a full-time employee working within a company's research team, offering stability and ongoing projects. A Contract Cra, on the other hand, works on temporary assignments, often through CROs, providing flexibility but less job security.

What are the key skills and qualifications needed to thrive as a Permanent In-House Clinical Research Associate (CRA), and why are they important?

To excel as a Permanent In-House CRA, you typically need a background in life sciences, strong knowledge of clinical trial processes, and a relevant degree (often in nursing, pharmacy, or biology). Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is highly valued. Attention to detail, excellent organizational skills, and strong communication abilities help build effective relationships with study sites and ensure study compliance. These competencies are crucial for maintaining regulatory standards, ensuring data integrity, and supporting the smooth execution of clinical trials.

How hard is it to get a CRA job?

Securing a permanent in-house CRA (Clinical Research Associate) position can be competitive, often requiring relevant experience, a degree in a related field, and industry certifications like the CCRP. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with clinical trial management systems can improve chances of hiring.

What is a Permanent In House CRA?

A Permanent In House CRA (Clinical Research Associate) is a professional who monitors clinical trials from within the sponsor or CRO’s office rather than traveling to investigator sites. They are responsible for supporting the management and oversight of clinical studies, ensuring compliance with protocols, regulatory requirements, and data integrity. Unlike field-based CRAs, In House CRAs typically handle documentation, query resolution, and site communication remotely. These roles are usually full-time, long-term positions within a company, offering job stability and opportunities for career growth.

How does a Permanent In House CRA typically collaborate with clinical project teams, and what are some common challenges in this coordination?

A Permanent In House Clinical Research Associate (CRA) works closely with clinical project managers, site monitors, data managers, and regulatory teams to ensure the smooth conduct of clinical trials. Collaboration often involves regular meetings, detailed documentation review, and timely communication to resolve site issues or protocol deviations. Common challenges include balancing multiple studies simultaneously, managing tight deadlines, and ensuring consistent communication between remote sites and the sponsor. However, being in-house allows for easier access to cross-functional support and resources, helping to address these challenges effectively.

What does an in-house CRA do?

An in-house Clinical Research Associate (CRA) monitors clinical trial activities within a company to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. They review data, coordinate with sites, and support trial documentation, often using electronic data capture (EDC) systems. This role requires strong attention to detail, knowledge of clinical processes, and relevant certifications such as a CRA certification.
What are the most commonly searched types of In House Cra jobs in California? The most popular types of In House Cra jobs in California are:
What are popular job titles related to Permanent In House Cra jobs in California? For Permanent In House Cra jobs in California, the most frequently searched job titles are:
What job categories do people searching Permanent In House Cra jobs in California look for? The top searched job categories for Permanent In House Cra jobs in California are:
What cities in California are hiring for Permanent In House Cra jobs? Cities in California with the most Permanent In House Cra job openings:
Infographic showing various Permanent In House Cra job openings in California as of July 2026, with employment types broken down into 11% Locum Tenens, 34% As Needed, 47% Full Time, 6% Part Time, 1% Contract, and 1% Summer. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution.
In-house Sr Clinical Research Associate

In-house Sr Clinical Research Associate

Solomon Page

San Diego, CA • On-site

$60 - $75/hr

Contractor

Medical, Dental, Vision, Retirement

Posted 21 days ago


Job description

A clinical-stage biopharmaceutical company in San Diego, California is seeking an experienced Contract Clinical Research Associate (CRA) to support ongoing clinical trials. This is an in-house clinical operations role (not a field monitoring position) with minimal travel required.
  • Pay rate: $60-75/hour
  • Location: California or Remote with travel to CA

Responsibilities:
  • Support clinical operations across multiple studies while ensuring subject safety and data integrity
  • Review and maintain the electronic Trial Master File (eTMF) in compliance with SOPs, GCP, and ICH guidelines
  • Support study start-up and ongoing trial activities, including regulatory documentation and site readiness
  • Serve as a liaison between internal teams, CROs, vendors, and investigator sites
  • Review monitoring visit reports (PSV, SIV, IMV, COV)
  • Remotely track enrollment and treatment status using IxRS and EDC systems
  • Maintain study tracking tools, meeting minutes, and action items
  • Participate in investigator meetings, study training, and co-monitoring activities as needed
  • Perform duties in compliance with FDA regulations, ICH-GCP, and company policies

Required Qualifications:
  • Bachelor's degree preferred
  • 4 years of In house CRA experience
  • Sponsor experience required
  • Site management and CRO/vendor oversight
  • Proficiency with Microsoft Office and Veeva eTMF required
  • Smartsheet and SharePoint a plus
  • Phase I-III Experience
    Clinical Resource Network Distinction
    CRN, a division of Solomon Page, offers a comprehensive benefits program for hourly employees. We pride ourselves on offering medical, dental, vision, 401(k), telehealth services, ESOP, and commuter benefits to our employees, including consultants - which sets us apart in the industries we serve.
    About CRN
    Founded in 2002, Clinical Resource Network (CRN), a division of Solomon Page, provides clinical research and talent solutions for pharmaceutical, biotech, and medical device companies. Focused on forming long-term relationships, services encompass contract staffing, project staffing, consultative services, and full-time placements. For more information, visit https://www.solomonpage.com/crn and connect with us on Facebook and LinkedIn .
    Opportunity Awaits.
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