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Cra Clinical Research Associate Jobs in Ridgewood, NJ

Msk

Clinical Research Associate

New York, NY · Hybrid

$62K - $97K/yr

Join our team as a Clinical Research Associate ! This position offers the opportunity to be part of meaningful, high-impact work where precision, compassion, and collaboration come together. Clinical ...

Icon plc

Senior CRA

New York, NY · On-site

$110K - $138K/yr

Senior CRA- Phase I Oncology/NJ/NY ICON is a global healthcare intelligence and clinical research ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...

Icon plc

Senior CRA

New York, NY · On-site

$110K - $138K/yr

Senior CRA Phase I Oncology- NY/NJ ICON is a global healthcare intelligence and clinical research ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...

Icon plc

Senior CRA

New York, NY · On-site

$110K - $138K/yr

Senior CRA- Phase I Oncology/NY/NJ ICON is a global healthcare intelligence and clinical research ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...

ICON

Senior CRA

New York, NY · On-site +1

$110K - $138K/yr

Senior CRA - Onc - NorthEast ICON is a global healthcare intelligence and clinical research ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...

Alira Health

Clinical Research Associate

Verona, NJ

Summary ROLE The Clinical Research Associate is an important member of the Alira Health Clinical team. CRAs are highly motivated and function independently to conduct site monitoring responsibilities ...

Pfizer

Senior Clinical Research Associate I

Manhattan, NY · On-site

$83 - $138/hr

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

IQVIA

Clinical Research Associate

Parsippany, NJ · On-site

$87K - $182K/yr

Req Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

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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

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

As of Sep 6, 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.

Senior Clinical Research Associate - Cardiovascular Medical Device

T45 Labs

New York, NY • On-site, Remote

Full-time

Posted 19 days ago

Job description

Senior Clinical Research Associate - Cardiovascular Medical Device
Status: Full-time, Exempt
Reports to: Senior Clinical Operations Manager
Location: Remote
Overview
VahatiCor is an early-stage cardiovascular medical device company developing break through cardiovascular technologies, including Class III catheter-based systems. We operate with a purpose-driven, agile, and collaborative culture, where each team member plays a meaningful role in advancing solutions that improve patient outcomes. As our clinical program grows, we are building a dedicated clinical operations team to support early feasibility studies and future pivotal trials.
The Senior Clinical Research Associate (CRA) will own site activation, clinical study startup, site management, enrollment performance, and protocol execution across VahatiCor's cardiovascular medical device clinical trials. This role serves as the primary operational partner to clinical sites, driving site readiness, investigator engagement, enrollment success, and consistent protocol execution throughout the study lifecycle. The ideal candidate brings deep experience in sponsor-side medical device clinical research, clinical operations, site management, and early-stage medical device clinical trials.
Responsibilities
Site Activation & Study Startup
  • Lead site qualification, feasibility, and readiness activities for assigned cardiovascular medical device clinical trial sites.
  • Own clinical study startup and site activation activities, including collection and review of essential regulatory and startup documentation.
  • Ensure investigators, study coordinators, and site personnel are prepared to enroll patients efficiently and compliantly.
  • Partner with the Clinical Trials Manager and study leadership on site contracting and budgeting activities and ensure timely site activation.
  • Track startup milestones and proactively identify and resolve activation barriers.

Site Management & Enrollment
  • Serve as the primary operational contact for assigned cardiovascular clinical trial sites
  • Build and maintain strong relationships with investigators, coordinators, and site personnel.
  • Drive patient screening and enrollment activities to achieve study recruitment goals.
  • Own site performance across assigned sites and implement actions to improve enrollment, protocol adherence, and study execution.
  • Partner with sites to address operational challenges and maintain study momentum.

Training & Clinical Study Execution
  • Conduct Site Initiation Visits (SIVs) and provide study-specific training to investigators and site personnel.
  • Deliver ongoing site education throughout study execution.
  • Ensure cardiovascular medical device clinical study activities are conducted in accordance with the protocol, Good Clinical Practice (GCP), applicable FDA medical device regulations, and company procedures.
  • Participate in investigator meetings, study team meetings, and site training activities.

Clinical Trial Monitoring & Quality
  • Conduct clinical trial monitoring activities as required to ensure study quality, compliance, and protocol adherence.
  • Review site documentation and study records for completeness and accuracy.
  • Identify protocol deviations, compliance concerns, and operational risks and escalate appropriately.
  • Ensure site documentation is complete, accurate, maintained in accordance with study requirements, and inspection-ready at all times.

Cross-Functional Collaboration
  • Partner cross-functionally with Clinical Operations, Clinical Affairs, Regulatory, and Quality to support effective study execution.
  • Communicate site feedback, enrollment trends, operational challenges, and emerging risks to study leadership.
  • Contribute to continuous improvement of site activation, enrollment, and study execution processes.

Required Experience & Qualifications
  • Bachelor's degree in Life Sciences, Nursing, Biomedical Engineering, or a related scientific discipline.
  • 7+ years of clinical research experience supporting medical device clinical trials.
  • Sponsor-side medical device clinical research experience is required. Candidates whose experience is primarily CRO-based without direct sponsor-side medical device experience will not meet the requirements for this role.
  • Prior clinical operations experience within an early-stage medical device company is required.
  • Demonstrated experience owning clinical study startup, site activation, patient enrollment, and clinical trial execution activities.
  • Experience owning site qualification, Site Initiation Visits (SIVs), clinical trial monitoring, and site management activities.
  • Cardiovascular medical device clinical trial experience is highly valued, particularly experience with catheter-based or other interventional cardiovascular technologies.
  • Demonstrated understanding of Good Clinical Practice (GCP), FDA medical device regulations, and clinical research operations.
  • Strong written and verbal communication skills.
  • Strong organizational, relationship-building, and problem-solving skills.
  • Ability and willingness to travel up to 60% to conduct site startup, activation, training, monitoring, and study execution activities.
  • Thrives in a dynamic, fast-paced, early-stage medical device environment where adaptability, initiative, and collaboration are critical to success.

Why Work for VahatiCor?
  • Help bring a first-of-its-kind therapy to patients with coronary microvascular dysfunction, a large and historically underserved patient population with limited treatment options.
  • Work alongside an experienced leadership team with deep expertise in cardiovascular medical devices, clinical research, regulatory affairs, and commercialization.
  • Make a visible impact in a collaborative, fast-moving environment where individual contributions directly influence the future of the technology, the clinical program, and the company.

Eligibility
Candidates must be permanently authorized to work in the United States without the need for current or future visa sponsorship. We are currently unable to sponsor employment visas or permanent residency (PERM) applications.
Location and Compensation
This is a remote position supporting clinical sites throughout the Eastern United States. We are prioritizing candidates who reside in the Eastern or Central time zone and are located within reasonable proximity to a major airport to support travel requirements. Travel of up to 60% is required based on study and site needs.
The anticipated annual base salary range for this position is $113,000 - $153,000. Actual compensation will be determined based on experience, qualifications, geographic location, and other job-related factors. VahatiCor is committed to fair and equitable pay practices. In addition to base salary, the total compensation package may include bonus opportunities, equity, and company-sponsored benefits.
Equal Opportunity Statement
VahatiCor is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Employment decisions are based on qualifications, merit, and business needs. We do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic.
Third-Party Recruiter Notice
We do not accept unsolicited resumes from staffing agencies or recruiters without a signed agreement in place. Any resumes submitted without such an agreement will be considered the property of VahatiCor and no fees will be paid if the candidate is hired. Agencies interested in submitting candidates may email careers@t45labs.com.

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