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Clinical Trial Jobs in Riverside, CA (NOW HIRING)

JenaValve

Specialist, Clinical Safety

Irvine, CA · On-site

$100K/yr

Contribute to clinical aspects of protocol development; specifically develop the Safety section of clinical trial protocols including adverse event definitions, AE reporting requirements, and risk ...

Kelly Services

Clinical Research Specialist

Irvine, CA · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

May serve as the primary contact for clinical trial sites (e.g. site management); * Assists in the development of clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring ...

Kelly Services

Clinical Research Specialist

Irvine, CA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Assists in the development of clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports * Supports applicable trial ...

Diality

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

Clinical Trial Administration * Assist with trial start-up, including preparing and submitting regulatory and ethics documents, such as IRB/EC submissions, contracts, and site feasibility ...

Diality Inc

Clinical Research Associate

Irvine, CA · On-site

$120K - $135K/yr

Clinical Trial Administration * Assist with trial start-up, including preparing and submitting regulatory and ethics documents, such as IRB/EC submissions, contracts, and site feasibility ...

Kaygen

Spec 3, Clinical Research

Irvine, CA · On-site

  • Medical

  • Life

  • Retirement

Support clinical trial start-up activities, including site readiness tracking, coordination of Site Qualification Visits (SQVs) and Site Initiation Visits (SIVs), and communication with investigative ...

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Showing results 21-40

All JobsClinical Trial JobsClinical Trial Jobs in Riverside, CA

Clinical Trial information

See Riverside, CA salary details

$30

$65

$100

How much do clinical trial jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for clinical trial in Riverside, CA is $65.22, according to ZipRecruiter salary data. Most workers in this role earn between $52.93 and $73.46 per hour, depending on experience, location, and employer.

What are clinical trials?

Clinical trials are research studies that involve human participants and are designed to evaluate the safety and effectiveness of new medical treatments, drugs, or devices. These trials follow a carefully controlled protocol and are conducted in phases to systematically assess outcomes. Participants may include patients with specific medical conditions or healthy volunteers, depending on the study's goals. The results from clinical trials help inform medical decisions and regulatory approvals for new therapies.

What are the key skills and qualifications needed to thrive in a clinical trial role?

To thrive in a Clinical Trial role, you need a solid understanding of clinical research principles, regulatory compliance, and data management, usually supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Strong attention to detail, organizational abilities, and effective communication skills help professionals coordinate complex processes and collaborate with interdisciplinary teams. These competencies are vital to ensure trials are conducted ethically, efficiently, and in compliance with regulatory standards.

What jobs are there in clinical trials?

Jobs in clinical trials include clinical research coordinators, clinical research associates, data managers, regulatory affairs specialists, and study nurses. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. The work environment is typically a research site, hospital, or pharmaceutical company, with schedules varying from standard to flexible hours depending on the role.

What are some common challenges faced by professionals working in clinical trial management, and how can they be addressed?

Professionals in clinical trial management often encounter challenges such as adhering to strict regulatory requirements, managing complex timelines, and ensuring effective communication among multidisciplinary teams. Overcoming these challenges typically involves thorough planning, continuous training on regulatory updates, and the use of project management tools to track progress and coordinate tasks. Building strong relationships with investigators and fostering open communication can also help address issues quickly and maintain trial integrity.

How to get into a clinical trial career?

A career in clinical trials typically requires a background in healthcare, life sciences, or related fields, along with knowledge of Good Clinical Practice (GCP) guidelines. Entry-level roles often require a bachelor's degree, and certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects. Gaining experience through internships or entry-level positions in research settings is also beneficial.

What are the most commonly searched types of Clinical Trial jobs in Riverside, CA?

The most popular types of Clinical Trial jobs in Riverside, CA are:

What are popular job titles related to Clinical Trial jobs in Riverside, CA?

For Clinical Trial jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Clinical Trial jobs in Riverside, CA look for?

The top searched job categories for Clinical Trial jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Clinical Trial jobs?

Cities near Riverside, CA with the most Clinical Trial job openings:

Clinical Trial jobs near you
Infographic showing various Clinical Trial job openings in Riverside, CA as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $135,661 per year, or $65.2 per hour.

Specialist, Clinical Safety

JenaValve

Irvine, CA • On-site

$100K/yr

Full-time

Re-posted 18 days ago

Job description

Job Title: Specialist, Clinical Safety
Role Level: Individual Contributor (IC)
Supervisor/Manager Title: Senior Manager, Clinical Safety
Job Location & Environment: Irvine, CA - Corporate Office
Job Description Summary: Reporting to the Senior Manager, Clinical Safety, the Specialist, Clinical Safety supports the conduct and timely execution of JenaValve clinical trials by monitoring subject safety, ensuring accurate and compliant adverse event data reporting in clinical databases, and contributing to the review and analysis of clinical safety data. The role collaborates closely with cross-functional teams including Project Management, Field Monitoring, Regulatory Affairs, and the Case Review Board to maintain the quality and integrity of safety data collected across all active trials, including the ALIGN-AR Pivotal Trial, JENA-VAD Registry, ALIGN-AR EFS Trial, and the ARTIST Trial.
Job Responsibilities:
  • Conduct assessments of adverse events (AEs) and complaints across multiple clinical studies, including UADE (Unanticipated Adverse Device Effect) determinations; perform complaint handling assessments and report AEs per regulatory requirements, trial safety processes, and JenaValve procedures.
  • Review and analyze aggregate safety reports to identify early safety signals; escalate findings to leadership with recommended next steps.
  • Track timeliness of AE and SAE reporting by investigational sites and follow up as needed to ensure compliance with protocol-specified timelines.
  • Interact with investigational sites and field monitors to obtain additional pertinent information on Case Report Forms and medical documentation (source documents).
  • Manage, prepare, and review event narratives for internal review or external reviews (e.g., Clinical Events Committee, Data Safety Monitoring Board) and for regulatory submissions.
  • Provide support to the MedDRA coding team on complex coding questions; participate in MedDRA coding team meetings and advise on important medical concepts.
  • Provide clinical and medical subject matter expertise to address safety-related questions from internal study teams, field support personnel, monitors, and study sites during the conduct of studies.
  • Contribute to clinical aspects of protocol development; specifically develop the Safety section of clinical trial protocols including adverse event definitions, AE reporting requirements, and risk sections.
  • Collaborate with data management and cross-functional teams on the development of case report forms, study-specific safety reports, and other study forms, ensuring alignment with clinical definitions and EDC data flows.
  • Support DSMB and CEC startup and management activities including vendor selection and approval, member selection, charter development, and ongoing conduct during clinical trials.
  • Lead site CRF development for AE Main Forms and AE Sub-forms; review edit checks and provide input into other CRF form development as needed.
  • Support PMA/APR activities including query closure, case narratives, and accurate presentation of endpoint-related data.
  • Assist the Clinical Safety team in daily safety reviews, data reconciliation, periodic reporting, and identification of necessary source documents.
  • Contribute to other clinical and medical affairs activities as needed and support continuous process improvement.
  • Complete training for internal SOPs and maintain current knowledge required for the role.

Required Education and Experience:
  • 2+ years of experience in clinical trial research required; medical device experience strongly preferred.
  • Bachelor's degree or higher in a life sciences, health sciences, or related field required; advanced clinical degree (NP, PA, MD, or international equivalent) highly preferred.
  • Working knowledge of HIPAA, ICH, GCP, and regulatory requirements related to clinical research.
  • Experience with cardiovascular or structural heart therapeutic areas is a significant advantage.
  • Strong organizational skills and time management abilities in a dynamic, fast-paced environment; ability to manage multiple concurrent priorities.
  • Excellent critical thinking skills and strong written and verbal communication skills.
  • Self-motivated, detail-oriented, and able to work independently as well as part of a collaborative team.

Skills and Abilities Required for This Job:
  • Clinical knowledge in cardiology; structural heart disease or transcatheter valve therapy experience preferred.
  • Knowledge of GCPs governing clinical trial conduct; working knowledge of medical device regulations and ICH guidelines.
  • Experience working across all phases of clinical study conduct from a clinical safety perspective.
  • Familiarity with MedDRA coding, adverse event terminology, and safety database management.
  • Experience with EDC (Electronic Data Capture) platforms for clinical trial management and safety reporting.
  • Basic understanding of clinical trial design and statistical concepts as applied to safety evaluation.
  • Ability to work collaboratively as part of a multi-functional medical device development team.
  • Excellent oral and written communication skills; strong interpersonal skills and ability to work effectively cross-functionally and cross-culturally.
  • Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).

Physical Requirements:
  • Standard office environment requirements.
  • Minimal travel, up to 10%.

Apply