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Cra Clinical Research Associate Jobs in Ridgewood, NJ

IQVIA

Clinical Research Associate

Parsippany, NJ · On-site

$71K - $189K/yr

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple Therapeutic Areas | Nationwide Opportunities IQVIA is actively seeking experienced Clinical Research ...

IQVIA

CRA 2/Senior CRA

New York, NY · On-site

$90K - $175K/yr

Join a Team That's Advancing Clinical Research We're looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical ...

Icon plc

Senior Clinical Research Associate

New York, NY · On-site

$110K - $138K/yr

Senior Clinical Research Associate- Northeast ICON is a global healthcare intelligence and clinical ... As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they ...

IQVIA

CRA 2/Senior CRA

New York, NY · On-site

$87K - $169K/yr

Join a Team That's Advancing Clinical Research We're looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical ...

IQVIA

CRA 2/Senior CRA 1

New York, NY · On-site

$90K - $175K/yr

Join a Team That's Advancing Clinical Research We're looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical ...

Pfizer

Clinical Research Associate

New York, NY

The Clinical Research Associate is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study ...

Pfizer

Clinical Research Associate

Manhattan, NY · On-site

$69 - $114/hr

The Clinical Research Associate is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study ...

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All JobsCra Clinical Research Associate JobsCra Clinical Research Associate Jobs in Ridgewood, NJ

Cra Clinical Research Associate information

See Ridgewood, NJ salary details

$12

$41

$70

How much do cra clinical research associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for cra clinical research associate in Ridgewood, NJ is $41.61, according to ZipRecruiter salary data. Most workers in this role earn between $29.18 and $53.27 per hour, depending on experience, location, and employer.

What is a clinical research associate?

CRA Clinical Research Associates are professionals who monitor clinical trials to ensure they are conducted in accordance with regulatory requirements, study protocols, and Good Clinical Practice guidelines. They act as a bridge between the sponsor of a clinical trial and the sites where the trial is conducted, overseeing data collection, patient safety, and compliance. Their responsibilities include site visits, reviewing documentation, and ensuring accurate reporting of study results. CRAs play a critical role in advancing medical research by maintaining the integrity and quality of clinical studies.

What are the key skills and qualifications needed to thrive as a clinical research associate?

To thrive as a Clinical Research Associate (CRA), you need a solid background in life sciences, experience in clinical trial monitoring, and typically a bachelor's degree in a related field. Familiarity with Good Clinical Practice (GCP) guidelines, electronic data capture (EDC) systems, and regulatory requirements is essential, and certifications like ACRP or SOCRA are often advantageous. Strong attention to detail, organizational skills, effective communication, and adaptability help CRAs excel in coordinating studies and collaborating with diverse stakeholders. These skills ensure clinical trials are conducted ethically, efficiently, and in compliance with regulatory standards, safeguarding both data integrity and patient safety.

What are some common challenges faced by clinical research associates when managing multiple clinical trial sites?

CRAs often juggle oversight of multiple clinical trial sites, which can present challenges such as coordinating visits, ensuring consistent protocol adherence, and managing varying site performance. Effective communication and strong organizational skills are crucial, as CRAs need to address site-specific issues, maintain accurate documentation, and ensure timely data collection. Additionally, adapting to diverse team dynamics and staying updated with regulatory requirements across sites are common aspects of the role. Employers typically provide training and support, but successful CRAs proactively develop strategies to manage these complexities.

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

AspectCra Clinical Research AssociateClinical Trial Coordinator
CredentialsTypically requires a bachelor's degree in life sciences, nursing, or related field; certifications like CCRP or RAC are commonUsually holds a bachelor's degree in health sciences, nursing, or related field; certifications like CCRP are also beneficial
Work EnvironmentWorks primarily on-site at clinical trial sites, monitoring study progress and complianceCoordinates trial activities, manages schedules, and ensures protocol adherence, often working at trial sites or offices
Employer & IndustryEmployed by pharmaceutical companies, CROs, or research institutions in the clinical research industryEmployed by hospitals, research centers, or pharmaceutical companies to manage trial logistics

While both roles support clinical trials, Cra Clinical Research Associates focus on monitoring and compliance, whereas Clinical Trial Coordinators handle trial logistics and coordination. Both require relevant certifications and work in similar environments within the clinical research industry.

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

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

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

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

Cra Clinical Research Associate jobs near you
Infographic showing various Cra Clinical Research Associate job openings in Ridgewood, NJ as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 17% Part Time, 6% Contract, and 1% Nights. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $86,550 per year, or $41.6 per hour.

Clinical Research Associate (CRA) - U.S. Expert Network | Project Opportunities | Remote

Alcedis GmbH

Manhattan, NY • On-site

$90 - $120/hr

Other

Posted 4 days ago

Job description

Alcedis is a well-established and successful clinical research organization headquartered in Germany, with over 30 years of experience in clinical research. Building on our strong track record in Germany, we are now taking the next step in our international growth by establishing our presence in the United States. As part of this expansion, we are building a network of experienced clinical research professionals who can support our current and future clinical studies.

We are looking for experienced Clinical Research Associates (CRAs) to join our U.S.-based expert network. Our current and anticipated projects focus primarily on Oncology and Alzheimer’s disease, with additional therapeutic areas expected to follow. Depending on project needs and mutual availability, members of our network may have the opportunity to support Alcedis as part-time W-2 employees on a project basis within our Clinical Operations team.

We are looking for a limited number of experienced CRAs to build a strong network of trusted clinical research professionals. Candidates will be reviewed based on their experience, qualifications, and fit with our current and future project needs.

When a suitable project becomes available, we will contact you to discuss the study, timing, workload, and your availability. If there is a mutual fit, you will be engaged as a part-time W-2 employee for the duration of the project.

You are welcome to continue working with other clients outside of your agreed assignment, subject to confidentiality and conflict-of-interest requirements.

Joining the expert network does not guarantee a project or minimum hours. If required, any project-specific qualification or pre-engagement activities involving actual work beyond the application and selection process will be compensated.

Qualifications and requirements

Required:

  • 3+ years of hands-on experience working as a Clinical Research Associate (CRA) / Clinical Monitor
  • Experience in GCP-regulated interventional clinical trials
  • Demonstrated experience in oncology clinical trials
  • Hands-on experience with digital solutions for clinical trials, such as ePRO, eCOA, and eCRF systems
  • Ability to work independently and proactively with a high degree of ownership
  • Experience with on-site monitoring and remote monitoring activities
  • Willingness to conduct and support Site Initiation Visits (primarily virtually) in the U.S. and Canada
  • Strong communication and organizational skills
  • Excellent written and spoken English
  • Based in the United States

Preferred:

  • Experience in Neurology and/or Alzheimer’s disease is a strong plus
  • Experience working in international or cross-border clinical research teams
  • Ability and flexibility to collaborate effectively across U.S. and European time zones, including regular interaction with colleagues based in Germany
  • Experience with U.S. and Canadian clinical trial requirements
  • Familiarity with FDA regulations, HIPAA, and 21 CFR Part 11

We welcome applicants of all backgrounds and do not discriminate based on race, ethnicity, gender, sexual orientation, disability, age, religion, or any other protected characteristic.

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