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Clinical Research Associate Jobs in Rutherford, NJ

Actalent

Clinical Research Nurse Coordinator

Livingston, NJ

$55 - $63/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Association of Clinical Research Professional as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP ...

Actalent

Clinical Research Nurse Coordinator

Livingston, NJ

$55 - $63/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Association of Clinical Research Professional as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP ...

Actalent

Clinical Research Nurse Coordinator

Livingston, NJ · On-site

$55 - $63/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Association of Clinical Research Professional as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP ...

Frontage Laboratories

Clinical Research Nurse

Secaucus, NJ · On-site

$45 - $55/hr

... Associate Director, and Clinical Research Coordinators. * Record study data in the source documents. Evaluate and review study data to ensure accuracy and completeness. * Develops a high level of ...

Rutgers University

Research Associate II

Piscataway, NJ · On-site

$65K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

Our clinical and academic facilities are located throughout the state including New Brunswick ... The Research Associate II will work with the Executive Director and Assistant Director to collect ...

Frontage Laboratories

Clinical Research Nurse

Secaucus, NJ · On-site

$45 - $55/hr

... Associate Director, and Clinical Research Coordinators. * Record study data in the source documents. Evaluate and review study data to ensure accuracy and completeness. * Develops a high level of ...

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

Clinical Research Associate information

See Rutherford, NJ salary details

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How much do clinical research associate jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for clinical research associate in Rutherford, NJ is $41.92, according to ZipRecruiter salary data. Most workers in this role earn between $29.42 and $53.65 per hour, depending on experience, location, and employer.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree such as a life sciences or healthcare-related field, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with clinical trial management systems can improve job prospects, but entry may be challenging for those without relevant qualifications or experience.

What is a clinical research associate?

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?

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.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and the chance to contribute to medical advancements, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in healthcare and research.

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.
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What are the most commonly searched types of Clinical Research jobs in Rutherford, NJ?

The most popular types of Clinical Research jobs in Rutherford, NJ are:

What job categories do people searching Clinical Research Associate jobs in Rutherford, NJ look for?

The top searched job categories for Clinical Research Associate jobs in Rutherford, NJ are:

What cities near Rutherford, NJ are hiring for Clinical Research Associate jobs?

Cities near Rutherford, NJ with the most Clinical Research Associate job openings:

Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Rutherford, NJ as of August 2026, with employment types broken down into 79% Full Time, 8% Part Time, and 13% Contract. Highlights an 52% In-person, 8% Hybrid, and 40% Remote job distribution, with an average salary of $87,204 per year, or $41.9 per hour.

Unblinded Clinical Research Coordinator II

DM Clinical Research

New York, NY

$26.50 - $35.25/hr

Full-time

Re-posted 4 days ago

Job description

Unblinded Clinical Research Coordinator II
DM Clinical Research is looking for an Unblinded Clinical Research Coordinator II to join our team in New Jersey. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

Duties amp; Responsibilities:
  • Compound and dispense prescribed IP.
  • Supervise and maintain records of all medications
  • Ensure compliance with study-specific blinding plans.
  • Provide consultative support regarding the preparation and dosing of drugs.
  • Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction.
  • Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials.
  • Understand and apply all applicable site procedures.
  • Ensure receipt and proper storage of IP and bioretention samples.
  • Manage inventory, ensuring that expired items are removed from the inventory prior to expiration, and purchasing, and delivery processes for the pharmacy.
  • Review protocols and provide input on clinical and pharmacy supply needs.
  • Meet with sponsors, monitors, auditors, and regulatory authorities to review drug accountability and other study-specific information.
  • Temperature reporting.
  • Any other duties/ tasks assigned by the manager, computer proficiency, especially Word, Excel, Outlook, and Google Docs.

Knowledge amp; Experience:
Education:
  • High School Diploma or equivalent required
  • Foreign Medical Graduate is a plus
  • Pharmacy Technician Certification a plus
Experience:
  • Clinical Experience
Credentials:
  • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant)
Knowledge and Skills:
  • Computer proficiency, especially Word, Excel, Outlook, and Google Docs.
  • Excellent communication and customer service skills.
  • Outgoing personality Well-organized with attention to detail.
  • Must be able to multitask.
  • Bilingual (Spanish) preferred but not required
DM Clinical Research, the largest privately-owned clinical research organization in the Houston area and one of the top fifty in the country, is looking for an Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

Duties amp; Responsibilities:
  • Compound and dispense prescribed IP.
  • Supervise and maintain records of all medications
  • Ensure compliance with study-specific blinding plans.
  • Provide consultative support regarding the preparation and dosing of drugs.
  • Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction.
  • Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials.
  • Understand and apply all applicable site procedures.
  • Ensure receipt and proper storage of IP and bioretention samples.
  • Manage inventory, ensuring that expired items are removed from the inventory prior to expiration, and purchasing, and delivery processes for the pharmacy.
  • Review protocols and provide input on clinical and pharmacy supply needs.
  • Meet with sponsors, monitors, auditors, and regulatory authorities to review drug accountability and other study-specific information.
  • Temperature reporting.
  • Any other duties/ tasks assigned by the manager, computer proficiency, especially Word, Excel, Outlook, and Google Docs.

Knowledge amp; Experience:
Education:
  • High School Diploma or equivalent required
  • Foreign Medical Graduate is a plus
  • Pharmacy Technician Certification a plus
Experience:
  • Clinical Experience
Credentials:
  • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant)
Knowledge and Skills:
  • Computer proficiency, especially Word, Excel, Outlook, and Google Docs.
  • Excellent communication and customer service skills.
  • Outgoing personality Well-organized with attention to detail.
  • Must be able to multitask.
  • Bilingual (Spanish) preferred but not required

Apply