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Crc Research Jobs (NOW HIRING)

Medix

Clinical Research Coordinator (CRC)

Nashville, TN · On-site

$25.93 - $32.41/hr

Bachelors Degree * 2 Years Experience CRC * Patient facing experience, no remote work Preferred Skills Oncology Research experience Schedule/Shift Monday-Friday 8am-5pm * We will consider for ...

GNP Research

Clinical Research Coordinator

Cooper City, FL

$22.25 - $29.50/hr

GNP Research is seeking an experienced Clinical Research Coordinator (CRC) to lead and manage clinical trials across various therapeutic areas. The ideal candidate is detail-oriented, proactive, and ...

GNP Research

Clinical Research Coordinator

Cooper City, FL

$22.25 - $29.50/hr

GNP Research is seeking an experienced Clinical Research Coordinator (CRC) to lead and manage clinical trials across various therapeutic areas. The ideal candidate is detail-oriented, proactive, and ...

University of Michigan

CRC- Assistant

Ann Arbor, MI · On-site

With guidance from faculty and research personnel, the clinical research assistant will support ... The CRC-assistant will also coordinate study visits and follow-up of study participants. The CRC ...

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Crc Research information

What are the key skills and qualifications needed to thrive as a CRC (Clinical Research Coordinator), and why are they important?

To thrive as a Clinical Research Coordinator (CRC), you need knowledge of clinical trial protocols, regulatory compliance, patient recruitment, and typically a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as CCRC or ACRP are highly valued. Strong organizational skills, attention to detail, and effective communication help build rapport with participants and ensure accurate data collection. These competencies are crucial for maintaining ethical standards, data integrity, and the successful execution of clinical studies.

What is the difference between Crc Research vs Crc Technician?

AspectCrc ResearchCrc Technician
CredentialsTypically requires a degree in chemistry, biology, or related fieldOften requires technical certifications or associate degree
Work EnvironmentLaboratory and research settingsFieldwork and laboratory environments
Industry UsageResearch institutions, biotech, pharmaceuticalsManufacturing, quality control, industrial settings

While both roles involve working with CRC (Cyclic Redundancy Check) concepts, Crc Research focuses on scientific investigation and development, often in labs, whereas Crc Technicians handle practical application, testing, and maintenance in industrial environments. The main difference lies in their focus: research versus technical implementation.

What are some common challenges faced by CRC Research professionals, and how can they be addressed?

CRC Research professionals often encounter challenges such as recruiting and retaining study participants, ensuring strict adherence to study protocols, and managing extensive regulatory documentation. To address these, it's helpful to develop strong communication skills, maintain organized records, and build rapport with participants. Collaborating closely with investigators, coordinators, and regulatory teams also helps ensure studies stay on track and compliant with all guidelines.

What are CRC Researchers?

CRC Researchers, or Clinical Research Coordinators, are professionals responsible for managing clinical trials and research studies in healthcare settings. Their duties include recruiting and screening participants, ensuring compliance with study protocols, collecting and managing data, and coordinating communication between investigators, sponsors, and participants. CRC Researchers play a vital role in maintaining the integrity and safety of clinical research, contributing to advancements in medical knowledge and patient care.
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Crc Research jobs near you
Infographic showing various Crc Research job openings in the United States as of May 2026, with employment types broken down into 1% Locum Tenens, 3% Internship, 6% Full Time, 81% Part Time, and 9% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution.

Clinical Research Coordinator (CRC) - Infectious Disease

Vitalief

Somerset, NJ • On-site

$65K - $80K/yr

Full-time

Medical, Life, Retirement, PTO

Posted 3 days ago

Job description

ABOUT VITALIEF
Vitalief is a trusted partner to Sponsors, CROs, and Sites across the research and clinical trials landscape.  By blending deep subject matter expertise with strong business acumen, we deliver Consulting and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients.​ 
POSITION SUMMARY
We are looking for an experienced Clinical Research Coordinator (CRC) to join Vitalief as a full-time employee with comprehensive benefits. This role will support an infectious disease clinical trial conducted at two community hospital sites in Rahway and Somerset, New Jersey, as part of a large pharmaceutical-sponsored study.  The ideal candidate will have at least two years of experience as a CRC, along with strong attention to detail, a genuine interest in clinical research, and the ability to work independently in a fast-paced environment.
This role requires a proactive, self-starting individual who can effectively manage patient-facing responsibilities while ensuring strict adherence to protocol requirements, regulatory standards, and specimen handling procedures. The CRC will work closely with the Principal Investigator (PI) and site leadership to support the successful execution of the study.
WHY VITALIEF?
  • Impactful Work: Contribute to scientific advancements that directly improve patient lives.
  • People-First Culture: Thrive in an environment that fosters growth, innovation, and collaboration.
  • Comprehensive Benefits: Enjoy 20 PTO days, 9 paid holidays, company-paid life insurance, short- and long-term disability, a 401(k) retirement plan, and robust healthcare options.
  • Work Location: Rahway, NJ and Somerset, NJ (travel required between the two sites)
  • Salary Range: $65,000 to $80,000 (depending on experience level).

Responsibilities:
  • Coordinate and execute day-to-day clinical trial activities across both sites in accordance with the study protocol, GCP, and regulatory requirements.
  • Work closely with the Principal Investigator (PI) to support study oversight, patient eligibility review, safety reporting, and protocol adherence.
  • Identify, screen, and consent eligible patients for participation in the study.
  • Schedule and manage patient visits, ensuring protocol compliance and timely completion of study procedures.
  • Serve as the primary point of contact for study participants, including meeting patients during visits and conducting follow-up communications.
  • Accurately collect, document, and maintain study data in source documents and electronic systems.
  • Ensure proper specimen collection, processing, storage, and shipment in compliance with protocol and laboratory requirements.
  • Collaborate with investigators, site staff, and sponsor representatives to ensure smooth study conduct.
  • Monitor patient safety and report adverse events per protocol and regulatory guidelines.
  • Maintain regulatory binders and ensure audit readiness at all times.
  • Support monitoring visits, audits, and inspections as needed.

Qualifications:
  • Bachelor’s degree required (healthcare, life sciences, or related field preferred).
  • Minimum of 2 years of experience as a Clinical Research Coordinator.
  • Prior experience working as a CRC in an Academic Medical Center (AMC) or community hospital setting is strongly preferred.
  • Experience in infectious disease studies preferred.
  • Strong understanding of Good Clinical Practice (GCP) and clinical trial processes.
  • Demonstrated ability to work independently and manage multiple priorities across two sites.
  • Enthusiastic and motivated team player; Self-starter with the ability to take initiative.
  • Excellent organizational skills and high attention to detail.
  • Strong interpersonal and communication skills, with a patient-centered approach.
  • Ability to problem-solve and adapt in a dynamic clinical environment.
  • Proficiency with electronic data capture (EDC) systems and Microsoft Office
  • Ability to work on-site role supporting two community hospital locations (Rahway, NJ and Somerset, NJ), requiring local travel between sites.

PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing. Lifting up to 20lbs.
IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.
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