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Clinical Research Associate Jobs in Riverside, NJ

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Clinical Research Nurse

Philadelphia, PA

Clinical Research Nurse III This Clinical Research Nurse III role combines advanced clinical ... Nursing Diploma or Associate's Degree in Nursing, with the ability to practice as a registered ...

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All JobsClinical Research Associate JobsClinical Research Associate Jobs in Riverside, NJ

Clinical Research Associate information

See Riverside, NJ salary details

$12

$41

$70

How much do clinical research associate jobs pay per hour?

As of Jun 20, 2026, the average hourly pay for clinical research associate in Riverside, NJ is $41.54, according to ZipRecruiter salary data. Most workers in this role earn between $29.13 and $53.17 per hour, depending on experience, location, and employer.

Is it hard to get a CRA job?

Securing a Clinical Research Associate (CRA) position can be competitive, often requiring relevant education, such as a degree in life sciences or healthcare, and experience with clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and certifications like CCRP can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or training programs.

What are Clinical Research Associates?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

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

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

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

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

What is the work of Clinical Research Associate?

A Clinical Research Associate (CRA) monitors clinical trials to ensure they are conducted according to protocols, Good Clinical Practice (GCP), and regulatory requirements. They coordinate with investigators, review trial data, conduct site visits, and ensure compliance, often using electronic data capture systems. CRAs play a key role in maintaining trial quality and integrity throughout the study process.

How much does a CRC make?

A Clinical Research Associate (CRA) in Houston typically earns between $60,000 and $85,000 annually, depending on experience, certifications, and the complexity of the clinical trials. Entry-level CRAs may start around $55,000, while experienced professionals with specialized skills can earn over $90,000. Salaries often include benefits such as health insurance and travel allowances, and the role requires knowledge of Good Clinical Practice (GCP) and clinical trial management tools.

What are some common challenges Clinical Research Associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

Can you be a CRA with no experience?

Becoming a Clinical Research Associate (CRA) typically requires some background in healthcare, life sciences, or related fields, but entry-level positions may be available for candidates with strong organizational skills and relevant certifications such as GCP training. Most employers prefer candidates with some related experience or education, but internships or training programs can provide a pathway for those without prior CRA experience.
More about Clinical Research Associate jobs
What are the most commonly searched types of Clinical Research jobs in Riverside, NJ? The most popular types of Clinical Research jobs in Riverside, NJ are:
What cities near Riverside, NJ are hiring for Clinical Research Associate jobs? Cities near Riverside, NJ with the most Clinical Research Associate job openings:
Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Riverside, NJ as of June 2026, with employment types broken down into 1% As Needed, 68% Full Time, 30% Part Time, and 1% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $86,397 per year, or $41.5 per hour.
Extramural Clin Research Coord

Extramural Clin Research Coord

Fox Chase Cancer Center

Philadelphia, PA

Full-time

Posted 10 days ago

Job description

This position supports the Fox Chase Cancer Center Office of Clinical Research at Temple University Hospital, Main Campus or East Norriton and Buckingham Campuses. Coordinates and facilitates the conduct of clinical research protocols, which includes the collection and handling of research specimens, documentation and shipment following IATA guidelines. Provides leadership in the management and operation of clinical research protocols to ensure research participant recruitment and accrual, protocol compliance, research participant safety and data quality.

Coordinates data management for satellite location. In addition, this position is expected to interact with the institutional investigators, other members of the healthcare team, service line members and research participants/families in a manner, which supports the conduct of clinical trials.Flexibility in work schedule when possible must be maintained to ensure coverage of study responsibilities. IATA Certification class will be provided within 3 months from date of hire.
Education
Bachelor's Degree Required
Graduate Level Classes or Degree in a relevant program Preferred or
Combination of relevant education and experience may be considered in lieu of degree Required
Experience
2 years experience in a healthcare setting preferably oncology or clinical trials Required
2 years experience with oncology clinical trials Preferred
1 year experience performing phlebotomy and specimen processing Preferred
General Experience and knowledge of chemotherapy and/or radiation therapy administration Preferred
Licenses
Cert Clin Research Coordinator Preferred
Cert Clin Research Prof Preferred
Cert Clin Research Associate Preferred

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