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Medical Research Associate Jobs in Riverside, CA

Envista

Sr. Research Scientist

Pomona, CA · On-site

$120K - $160K/yr

Provide mentoring/coaching to research associates and research chemists. * Represent R&D in product ... Master's degree in chemistry, polymer, or related fields required with 5 years within the medical ...

Orion Group

Scientific Writer

Orange, CA · On-site

$32 - $35/hr

... Associate with a focus on scientific writing) to join our dynamic team. This role involves ... medical research to contribute to innovative healthcare solutions within a collaborative ...

CIBD

Research Intern

Orange, CA

Requirements Actively enrolled in either an undergraduate Bachelor's degree (or Associate's degree ... expert comprehensive diagnosis, medical care, outreach, education, outcomes monitoring ...

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All JobsMedical Research Associate JobsMedical Research Associate Jobs in Riverside, CA

Medical Research Associate information

See Riverside, CA salary details

$39.1K

$55.6K

$61K

How much do medical research associate jobs pay per year?

As of Jun 12, 2026, the average yearly pay for medical research associate in Riverside, CA is $55,634.00, according to ZipRecruiter salary data. Most workers in this role earn between $56,300.00 and $60,500.00 per year, depending on experience, location, and employer.

How hard is it to get a CRA 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 organizational skills, knowledge of Good Clinical Practice (GCP), and certification such as CCRP can improve chances, but entry may be challenging for those without related experience or training.

How much does a CRC make?

A Clinical Research Coordinator (CRC) in Houston typically earns between $50,000 and $70,000 annually, depending on experience, certifications, and the employer. Salaries can vary based on the complexity of trials and the research environment.

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

AspectMedical Research AssociateClinical Research Coordinator
CredentialsBachelor’s degree in life sciences or related field; certifications like CCRP are commonBachelor’s degree in health sciences, nursing, or related; often holds certifications like CCRP or CCRC
Work EnvironmentResearch labs, pharmaceutical companies, academic institutionsHospitals, clinics, research sites
Employer & IndustryPharmaceutical companies, biotech firms, academic research centersHospitals, clinical trial sites, research organizations
Common Search & ComparisonMedical Research Associate vs Clinical Research Coordinator

Both roles involve coordinating and supporting clinical research, but Medical Research Associates typically focus on data collection, analysis, and supporting laboratory work, while Clinical Research Coordinators manage patient recruitment, scheduling, and regulatory compliance at research sites. The roles often overlap, but their primary responsibilities and work environments differ slightly.

Can you be a CRA with no experience?

A Clinical Research Associate (CRA) typically requires prior experience in clinical trials or related healthcare fields, as the role involves monitoring study sites and ensuring compliance. Entry-level positions may be available for those with relevant educational backgrounds, strong organizational skills, and knowledge of Good Clinical Practice (GCP) guidelines, but most employers prefer candidates with some related experience or training. Certifications such as the CCRP can also enhance prospects for those new to the field.

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

To thrive as a Medical Research Associate, you need a strong background in life sciences, data analysis, and clinical research methods, often supported by a relevant degree such as biology or pharmacology. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and statistical analysis software is typically required. Attention to detail, critical thinking, and effective communication are standout soft skills for this role. These abilities ensure accuracy, regulatory compliance, and successful collaboration in conducting and managing clinical studies.

What are some common challenges faced by Medical Research Associates when coordinating clinical trials?

Medical Research Associates often encounter challenges such as managing tight timelines, ensuring strict adherence to regulatory guidelines, and maintaining clear communication among diverse teams. Coordinating with investigators, sponsors, and regulatory bodies requires strong organizational and interpersonal skills. Additionally, balancing multiple studies simultaneously can be demanding, making effective time management and attention to detail essential for success in this role.

What are Medical Research Associates?

Medical Research Associates are professionals who assist in the planning, coordination, and execution of clinical trials and medical research studies. They ensure that studies comply with regulatory guidelines and ethical standards, collect and analyze data, and help prepare reports for publication. Their work is essential in advancing medical knowledge and supporting the development of new treatments and therapies.

What does a medical research associate do?

A medical research associate (MRA) supports clinical trials by coordinating study activities, ensuring compliance with protocols, collecting and managing data, and monitoring patient safety. They often work closely with investigators, use data management tools, and may require knowledge of Good Clinical Practice (GCP) guidelines. The role typically involves detailed documentation and adherence to regulatory standards.
What are the most commonly searched types of Medical Research jobs in Riverside, CA? The most popular types of Medical Research jobs in Riverside, CA are:
What are popular job titles related to Medical Research Associate jobs in Riverside, CA? For Medical Research Associate jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Medical Research Associate jobs in Riverside, CA look for? The top searched job categories for Medical Research Associate jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Medical Research Associate jobs? Cities near Riverside, CA with the most Medical Research Associate job openings:
Medical Research Associate jobs near you
Infographic showing various Medical Research Associate job openings in Riverside, CA as of June 2026, with employment types broken down into 45% Full Time, 32% Part Time, and 23% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $55,634 per year, or $26.7 per hour.

Senior Clinical Research Scientist

Johnson & Johnson

Irvine, CA • Hybrid

Full-time

PTO

Posted yesterday

Johnson & Johnson rating

8.1

Company rating: 8.1 out of 10

Based on 101 frontline employees who took The Breakroom Quiz

31st of 71 rated pharmaceutical

Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Discovery & Pre-Clinical/Clinical Development

Job Sub Function:

Clinical Development & Research - Non-MD

Job Category:

Scientific/Technology

All Job Posting Locations:

Irvine, California, United States of America

Job Description:

Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that's reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

We are searching for the best talent for a Senior Clinical Research Scientist to support our Electrophysiology business. This role will work a Flex/Hybrid schedule with 2-3 days per week onsite in our Irvine, CA office.

The Senior Clinical Research Scientist will join the Clinical Science & External Research (CSER) Team responsible for global evidence generation and dissemination of scientific findings from clinical trials and registries sponsored by Johnson & Johnson MedTech Electrophysiology. This associate will play a critical role in the creation and delivery of accurate, high-quality scientific content that communicates clinical and real-world data on the Company's Electrophysiology medical devices. This role is responsible for running real-world evidence studies and supporting evidence generation strategy. The ideal candidate will have strong scientific writing experience, deep familiarity with the cardiovascular and/or electrophysiology clinical landscapes, and a thorough understanding of clinical trials, regulatory guidelines, and clinical study design.

Key Responsibilities:

  • Produce clinical study protocols and clinical study reports, ensuring scientific soundness and compliance with regulatory requirements
  • Conducts literature & landscape reviews to identify concepts of importance to patients to inform evidence strategy
  • Support and coordinate multiple real-world evidence research studies in partnership with external groups: participating study site staff, Clinical Research Organizations (CRO), and vendors, and with internal teams: medical affairs, data management, biostatistics, data programmers, and regulatory affairs
  • Manage with supervision clinical trials including study budget assessment, fair mark value appraisal, contract development and execution, payments, and development of study related materials
  • Ensure clinical research studies follow regulatory standards and maintain accurate, detailed documentation for audits and submissions
  • Develop and deliver high-quality scientific manuscripts, abstracts, posters, and podium presentations for publication in peer-reviewed journals and presentation at major cardiovascular and Electrophysiology congresses
  • Collaborate closely with internal cross-functional teams (Clinical, Biostatistics, Medical Affairs, Global Strategic Marketing, Health Economics and Market Access) and external physician authors to ensure accuracy, alignment, and scientific integrity
  • Analyze and interpret clinical data; effectively communicate data using well-structured tables and visually compelling figures
  • Support the strategic evidence planning for key products and studies, including first-in-human trials, pivotal studies, indication expansions, post-market surveillances, and registries
  • Engage with Clinical Science & External Research associates and cross-functional teams to develop evidence strategy
  • Adhere to external guidelines and Company policies governing the ethical development of clinical data publications while continuing to look at innovation in publication and scientific communications
  • Maintain awareness of emerging trends and competitors in cardiovascular and electrophysiology therapy spaces to inform content development
  • Stays on top of current scientific data by participating in monthly literature review and sharing key insights with global teams

Qualifications

Required:

  • Minimum of a bachelor's degree in Life Sciences, Physical Science, Nursing, Biological Science, or closely related field
  • Minimum of 2 years of direct involvement in clinical research trials and scientific publications in a medical industry or related setting
  • Excellent written and oral communication skills
  • Strong project management skills to balance multiple projects
  • Excellent interpersonal skills, with the ability to build relationships and collaborate effectively with key partners across different time zones
  • Demonstrated adaptability in fast-paced, evolving environments
  • Knowledge of Good Clinical Practices, Evidence Generation Strategy, and ICMJE standards

Preferred:

  • PhD/MD/PharmD with industry/academic research experience
  • 3+ years of experience in cardiovascular and/or electrophysiology therapeutic areas
  • Prior experience designing and executing clinical studies
  • ISMPP CMPP or AMWA MWC credentials
  • Knowledge of electrophysiology procedures and terminology

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers. Internal employees contact AskGS to be directed to your accommodation resource.

#LI-Hybrid

Required Skills:

Preferred Skills:

Analytical Reasoning, Clinical Data Management, Clinical Evaluations, Clinical Trial Protocols, Coaching, Consulting, Data Savvy, Drug Discovery Development, Good Clinical Practice (GCP), Medicines and Device Development and Regulation, Persistence and Tenacity, Regulatory Affairs Management, Research Documents, Resource Management, Safety-Oriented, Scientific Research, Technologically Savvy

The anticipated base pay range for this position is :

$92,000.00 - $148,350.00

Additional Description for Pay Transparency:

Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation -120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year
Holiday pay, including Floating Holidays -13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave - 80 hours in a 52-week rolling period10 days
Volunteer Leave - 32 hours per calendar year
Military Spouse Time-Off - 80 hours per calendar year
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

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