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In Vivo Research Associate Jobs in Riverside, CA

JenaValve

Associate, Clinical Research

Irvine, CA · On-site

$75K/yr

The Clinical Research Associate will report to the Director, Clinical Affairs, and will play a key role in proactively supporting the conduct of pre-market and or post-market clinical studies and ...

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All JobsIn Vivo Research Associate JobsIn Vivo Research Associate Jobs in Riverside, CA

In Vivo Research Associate information

See Riverside, CA salary details

$17

$33

$48

How much do in vivo research associate jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for in vivo research associate in Riverside, CA is $33.95, according to ZipRecruiter salary data. Most workers in this role earn between $27.36 and $38.61 per hour, depending on experience, location, and employer.

What is an in vivo research associate?

In Vivo Research Associates are laboratory professionals who conduct scientific experiments and studies on live animals to understand biological processes, test new drugs, or evaluate the safety and efficacy of medical treatments. They work closely with scientists, veterinarians, and other research staff to ensure studies are conducted ethically and in compliance with regulatory standards. Their responsibilities often include animal handling, administering treatments, collecting biological samples, and recording data. The role is important in preclinical research, especially within the pharmaceutical and biotechnology industries.

What are some common challenges faced by in vivo research associates, and how can they be addressed?

In Vivo Research Associates often encounter challenges such as managing complex animal studies, ensuring compliance with regulatory standards, and handling unexpected experimental variables. Balancing multiple projects and maintaining meticulous records can also be demanding. To address these challenges, strong organizational skills, effective communication with team members, and ongoing training in animal care protocols are essential. Collaborating closely with scientists and veterinarians helps ensure studies run smoothly and data integrity is maintained.

What are the key skills and qualifications needed to thrive as an in vivo research associate, and why are they important?

To thrive as an In Vivo Research Associate, you need a strong background in biology or related sciences, animal handling experience, and often a bachelor's degree in a life science field. Familiarity with laboratory animal protocols, data collection systems, and certifications such as AALAS are typically required. Attention to detail, strong organizational skills, and effective teamwork are essential soft skills for success in this role. These skills ensure ethical treatment of animals, reliable experimental results, and efficient collaboration within research teams.
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In Vivo Research Associate jobs near you
Infographic showing various In Vivo Research Associate job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $70,614 per year, or $33.9 per hour.

Associate, Clinical Research

JenaValve

Irvine, CA • On-site

$75K/yr

Full-time

Re-posted 11 days ago

Job description

Job Title: Associate, Clinical Research
Role Level: Individual Contributor (IC)
Supervisor/Manager Title: Director, Clinical Affairs
Job Location & Environment: Irvine, CA, Corporate Office
Job Description Summary: The Clinical Research Associate will report to the Director, Clinical Affairs, and will play a key role in proactively supporting the conduct of pre-market and or post-market clinical studies and ensure compliance with all regulatory requirements. The ideal candidate will have a thorough knowledge of Good Clinical Practices (GCP) and applicable regulations.
Job Responsibilities:
  • Support site management and interact with site coordinators, investigators, and field monitors in collecting data and resolving queries to meet the protocol requirements in a timely manner.
  • Ensure quality data management activities - i.e., data review, query generation and resolution. Generate status reports to clinical staff and management.
  • Maintain Trial Master Files and trackers for clinical trials.
  • Manage trial-related regulatory documents and provide follow-up action listings to ensure that all clinical documentation required by regulations and JenaValve procedures is current.
  • Conduct periodic audits of internal files to ensure compliance per site Institutional Review Board (IRB) and/or Ethics Committee (EC) policy (i.e. IRB continuing review approval period and expiration dates).
  • Provide clinical operational support during preparation for and conduct of all clinical audits and inspections.
  • Contribute to the development and implementation of departmental policies, standards, and process improvement initiatives.
  • Partner with management to manage external vendors, including ongoing supplier qualification.
  • Assist field clinical monitors in preparation for site training and monitoring visits
  • Support monitoring of sites on an as-needed basis.

Required Education and Experience:
  • At least 1 year of experience in clinical trial research is required (preferred in medical devices).
  • Advanced degree in a biological science / pharmacy/ nursing desired.

Skills and Abilities Required for This Job:
  • Proficient in clinical trial management and electronic data capture systems to document and record information.
  • Excellent communication skills (written and verbal English) so as to be able to build effective relationships with trial center staff and colleagues.
  • Some knowledge of GCPs governing the conduct of clinical trials, Medical Device Directive 93/42/EEC, ISO14155 and ICH guidelines.
  • Very organized and able to pay close attention to detail.
  • Team player with a willingness to help where needed and work with diverse people.

Physical Requirements
  • Ability to travel up to 20% time.

Apply