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Medical Research Associate Jobs in Riverside, CA

Research Associate III

Pomona, CA · On-site

$83K - $101K/yr

The Research Associate III will be primarily responsible for independently designing, executing ... Minimum of 2 years working in the medical device or pharmaceutical industry preferred. Skills and ...

Research Associate I

Pomona, CA · On-site

$70K - $75K/yr

The Research Associate I will be responsible for supporting compliance with the company's current ... medical/dental/vision benefits, 401K match, and/or other applicable compensation plans. $70,400 ...

Research Associate I

Pomona, CA · On-site

$70K - $75K/yr

The Research Associate I will be responsible for supporting compliance with the company's current ... medical/dental/vision benefits, 401K match, and/or other applicable compensation plans. $70,400 ...

Research Associate I

Irvine, CA · On-site

$70K - $77K/yr

Overview The Research Associate I , will spend the day executing laboratory experiments in support ... Benefits: We're proud to offer a variety of options, including competitive medical plans for you ...

Clinical Research Associate

Irvine, CA · On-site

$120K - $135K/yr

The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... g., medical affairs, field service, clinical operations, clinical training and support), and ...

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... g., medical affairs, field service, clinical operations, clinical training and support), and ...

Associate, Clinical Research Role Level: Individual Contributor (IC) Supervisor/Manager Title ... At least 1 year of experience in clinical trial research is required (preferred in medical devices)

Associate, Clinical Research Role Level: Individual Contributor (IC) Supervisor/Manager Title ... At least 1 year of experience in clinical trial research is required (preferred in medical devices)

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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 Jul 18, 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.

What qualifications do you need to be a research associate?

A research associate in the medical field typically needs at least a bachelor's degree in a related science or healthcare discipline, such as biology, chemistry, or nursing. Relevant skills include data analysis, laboratory techniques, and familiarity with research protocols; some positions may require a master's degree or higher. Certifications like Good Clinical Practice (GCP) or Good Laboratory Practice (GLP) can also be advantageous.

Is it hard to get a CRA job?

Securing a Clinical Research Associate (CRA) position can be competitive, often requiring relevant experience, a degree in life sciences or related fields, and knowledge of Good Clinical Practice (GCP) guidelines. Entry-level roles may be easier to obtain with strong educational backgrounds and certifications like the CCRP, but advancing to senior CRA positions typically demands proven experience in clinical trials and monitoring skills.

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.

Is CRA better than CRC?

A Clinical Research Associate (CRA) and a Clinical Research Coordinator (CRC) are both key roles in clinical trials, but they have different responsibilities. CRAs typically oversee multiple sites, monitor trial progress, and ensure compliance, often working remotely or traveling frequently, while CRCs manage day-to-day trial activities at a specific site, including patient recruitment and data collection. Both roles require knowledge of Good Clinical Practice (GCP) and relevant certifications, but CRAs usually have more experience and may require a background in monitoring or regulatory aspects.

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 require knowledge of Good Clinical Practice (GCP) standards. The role typically involves documentation, communication, and adherence to regulatory requirements.
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:
Research Associate

$17/hr

Full-time

Retirement, PTO

Re-posted 11 days ago


Western University Of Health Sciences rating

7.9

Company rating: 7.9 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

182nd of 555 rated colleges and universities


Job description

Posting Details
About WesternU
As you take your first step onto a Western University of Health Sciences campus, each path, each person, each structure comes with a transformative story. WesternU is more than the practice of medicine. We are defined by character and culture.
At WesternU, you will discover humanism at the heart of every interaction: a warm welcome, a sincere smile, a positive word, a kind deed, a thoughtful gesture. You will see students work together on case studies; a parade of pets in campus parks; student clubs offering opportunities for career growth and community involvement; and faculty, staff and students designing their future and the future of WesternU. We display a collaborative mindset in how we operate, educate, and serve others.
Although, geographically, we are two campuses - as humanists, we are one: to enhance and extend the quality of life in our communities and achieve excellence in everything we do. We attract diverse, professional faculty, staff and students that thrive in an environment of humanistic health care education. Join our team of faculty and staff and make a difference.
Posting Details
Position Title
Research Associate
Position Control Number
S03517
Type of Position
Staff
Position Status
Full-time
Campus
Western University Campus-Pomona, CA
Position Location
Department
6011-Center for Clinical Research
Job Summary
Responsibilities include execution of the study protocol per all study design plans and SOPs related to study conduct, including project management support for studies. These responsibilities may include but are not limited to sample preparation, dose verification, study system dosing, sample analysis and re-analysis, data collection and recording data either manually or electronically, sign offs on all scientific aspects of study participation. Research Associates must work closely with study directors, contributing scientists, veterinary and clinical support services, pathology, quality assurance, regulatory affairs, and analytical/bio analytical services to ensure all study aspects are conducted per scientific and regulatory requirements.
Knowledge, Skills and Abilities
Descriptive statistics, formulation and dosing calculations, dilutions, etc; excellent communication and technical writing skills; proactive in spotting potential problems and seeking successful solutions; excellent attention to detail.
Familiarity with clinical/veterinary terminology pertaining to dosing, clinical observations, physiology, pathology, animal behavior, etc.
Required Qualifications
B.S. or equivalent in a scientific area (i.e. biology, veterinary sciences); minimum 2 years experience in clinical area or preclinical and experimental animal research; experience with molecular and biochemical techniques; experience with histological procedures; knowledge of vivarium and/ or in vivo procedures and processes, including preclinical study implementation and conduct
Preferred Qualifications
Optometry degree, Medical degree, clinical lab scientist are preferred. License to practice is not needed
Essential Job Duties
Key Responsibilities
Manage and assist with implementing and performing clinical data collection, interaction with human subjects, in-vitro and in-vivo projects including surgeries, necropsies, behavioral testing, biochemical assays, etc., from study initiation to study completion.
Key Responsibilities
Provide project management support for studies, in addition to qc oversight for data and assistance in generating reports for clients and internal committees.
Key Responsibilities
Responsible for all in vivo data collection and archiving, and generation of draft study reports. Assure adherence to protocol, amendments, sops, glp (if applicable) and regulatory compliance throughout the conduct of studies.
Key Responsibilities
Create and interpret scientific documents including study protocols, SOPs and regulatory guidelines.
Key Responsibilities
Experimental subjects contact and examination or animal handling, including treatments, blood sampling (including subcutaneous, intramuscular, intravenous, intraperitoneal and intradermal routes), and tissue collection in various rodent species. Must perform various technical tests on human subjects and may perform other technical procedures on study animals as needed.
Posting Details Continued
Work Schedule
Monday to Friday and some weekends
Working at WesternU
We believe in making an impact in the lives of our employees, personally, and professionally. Every employee has different individual and/or family needs. We offer benefits that are both comprehensive and flexible to address your unique needs. We believe work-life harmony is positive and achievable.
We offer competitive salaries, generous paid time off, insurance plans, reimbursements, and retirement benefits. Additionally,
• Our faculty, staff, and administrators are 100% focused on student success.
• Our University culture creates the context for a nurturing and supportive environment.
• Faculty, staff, and students can expect to make deep, personal relationships within the University community.
• As a Faculty, Staff, or Student at WesternU, you can focus on work that you love, be your authentic self, and lead to the future with innovation in health sciences.
• WesternU's core value of humanism encourages all to bring their whole self in all that they do.
• We are committed to fostering a culture of respect, equity, collaboration, and fun at all levels for all people!
Expected Pay Scale
Minimum
$17.00
Maximum
$17.00

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