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Senior Clinical Research Associate Jobs in Ridgewood, NJ

Touro University

Clinical Research Associate

Hawthorne, NY · On-site

$48K - $60K/yr

Ensure compliance with the Good Clinical Practice guidelines in clinical research. * Monitor study patients for adverse events in collaboration with clinical team and report as required. * Enter data ...

Montefiore

Research Associate III (JR226738)

Bronx, NY · On-site

OverviewThe Cancer Clinical Trials Senior Research Associate supports the research team in the overall conduct of clinical trials using Good Clinical Practice. The Senior Research Associate is able ...

IQVIA

Clinical Research Associate

Parsippany, NJ

$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.

ICON

Clinical Research Associate - Oncology

New York, NY · On-site +1

$91K - $114K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Research Associate - Oncology - ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a ...

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Senior Clinical Research Associate information

See Ridgewood, NJ salary details

$36.4K

$95.4K

$145.2K

How much do senior clinical research associate jobs pay per year?

As of Aug 19, 2026, the average yearly pay for senior clinical research associate in Ridgewood, NJ is $95,426.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,200.00 and $129,500.00 per year, depending on experience, location, and employer.

What does a senior clinical research associate do?

A senior clinical research associate (CRA) monitors clinical trials and manages team members. Your duties include leading project team meetings, running experiments, making observations, tracking results, and analyzing data. You also ensure experiments meet all clinical practice and safety standards. Qualifications for this career are a bachelor of science in a biomedical field or a bachelor of science in nursing (BSN), along with professional experience in a medical or research setting. You must have strong communication, interpersonal, leadership, and technical writing skills.

What are the key skills and qualifications needed to thrive as a senior clinical research associate, and why are they important?

To thrive as a Senior Clinical Research Associate, you need a solid background in clinical research, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong organizational skills, attention to detail, and the ability to communicate effectively with diverse stakeholders make someone stand out in this position. These skills and qualities are vital for ensuring studies are conducted ethically, accurately, and in compliance with regulatory standards.

What are some typical challenges faced by senior clinical research associates when overseeing multiple clinical trials?

Senior Clinical Research Associates (SCRAs) often manage several studies at once, which requires balancing competing deadlines, ensuring protocol compliance, and maintaining strong communication with site staff. A common challenge is ensuring consistent data quality and regulatory adherence across diverse sites, especially when trials are geographically dispersed. Effective time management, attention to detail, and proactive problem-solving are crucial for success in this role. Collaboration with project managers, investigators, and regulatory teams is also essential to ensure trials progress smoothly and meet all regulatory requirements.
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Clinical Research Associate

New York Medical College

Hawthorne, NY • On-site

$48K - $60K/yr

Full-time

Re-posted 5 days ago

Job description

Overview
Responsible for pre-clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen collection and transmittal, data collection and management, adverse event management to ensure protocol compliance in conjunction with the PI, clinical team and clinical research nurses and team.
Responsibilities
  • Assist in new IRB application and annual renewal process of COG, sponsored, local and other multi-institutional protocols.
  • Screen and enroll patients onto clinical trials in collaboration with clinical team, ensure protocol compliance; coordination of specimen collection and transmittal in collaboration with clinical team.
  • Ensure compliance with the Good Clinical Practice guidelines in clinical research.
  • Monitor study patients for adverse events in collaboration with clinical team and report as required.
  • Enter data on Hematology, Oncology and Stem Cell Transplant patients on electronic data capture forms; prepare for routine data audits and maintain source documents and regulatory binders. Manage communications- mail, phone, fax, e-mail for COG, sponsored, local and multi-institutional studies. Act as liaison between NYMC and Westchester Medical Center, regarding new study requirements.

Qualifications
Education requirement: BS
Other skills/requirements: Must have a keen attention to detail, be able to multi-task and prioritize assignments.
Minimum Salary
USD $48,000.00/Yr.
Maximum Salary
USD $60,000.00/Yr.

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