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Crc Research Jobs (NOW HIRING)

LINQ Research, LLC

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Clinical Research Coordinator (CRC)

Pearland, TX · On-site

$58K - $65K/yr

Clinical Research Coordinator (CRC) LINQ Research, LLC Location: Pearland, TX -0 Onsite Job Type: Full-Time Schedule: Monday-Friday, 8:00 AM-5:00 PM Department: Clinical Research Reports To: Site ...

One of a Kind Clinical Research Center LLC

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Clinical Research Coordinator (CRC)

Kingwood, TX · On-site

$23 - $28/hr

Clinical Research Coordinator (CRC) Kingwood, Texas | On-site We are seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to join our team in Kingwood, TX. This position is ...

Nrel

Adversarial Cybersecurity Researcher

Golden, CO · Hybrid

CRC research spans threat actor modeling and simulation, operational technology (OT) risk analysis, adversarial experimentation, hardware and software assurance, supply chain integrity, and cyber ...

Neurology Rare Disease Center

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Clinical Research Coordinator (CRC)

Flower Mound, TX · On-site

$50K - $70K/yr

Position Summary We are seeking a highly motivated and detail-oriented Clinical Research Coordinator (CRC) to oversee and manage clinical trials from start-up through close-out. This role requires ...

Insight

Clinical Research Coordinator I (CRC-1)

Chicago, IL · On-site

$50K - $65K/yr

Director of Clinical Trials and Clinical Research Coordinator III - Team Lead Position Summary The Clinical Research Coordinator I (CRC I) is responsible for supporting the conduct of clinical trials ...

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Crc Research information

What is a CRC researcher?

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.

What skills and qualifications are needed to thrive as a CRC?

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 are 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 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 is the role of a CRC Research in research?

A CRC Research typically refers to a Clinical Research Coordinator involved in managing clinical trials, ensuring protocol adherence, recruiting participants, and collecting data. They coordinate between researchers, participants, and regulatory bodies, often requiring knowledge of Good Clinical Practice (GCP) and relevant software tools. Their role is essential for the successful execution and compliance of research studies.
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Crc Research jobs near you
Infographic showing various Crc Research job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 84% Full Time, 11% Part Time, 1% Temporary, and 2% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution.

Clinical Research Coordinator (CRC)

Azimuth Research Group

Portsmouth, VA • On-site

$60 - $80/hr

Other

Posted 4 days ago

Key responsibilities

  • Coordinate operational aspects of clinical research projects across assigned study sites, including military treatment facilities.

  • Support the development, maintenance, and review of regulatory documents such as ICFs, protocol amendments, and IRB submissions.

  • Assist in participant screening, eligibility verification, recruitment tracking, and scheduling in alignment with protocol requirements.

Job description

Company Overview

Azimuth Research Group (Azimuth) is a global research organization that leverages point of care data to address challenging questions for clients in the pharmaceutical and biotechnology industry, as well as academia. Our vision is to remake the biopharmaceutical and overall research industry by embedding continuous, adaptive research into healthcare delivery ecosystems. We accelerate the discovery and development of therapies with intelligent precision–ultimately improving patient outcomes globally.

Work Location

Hampton Roads Area (Portsmouth, VA)

Job Title

Clinical Research Coordinator (CRC)

Job Status

Full-time Employment

Job Summary

The CRC is responsible for day-to-day clinical trial coordination activities including site communication, participant screening support, data collection oversight, regulatory documentation, and protocol compliance. This role requires working knowledge of the DoD Military Health System, including familiarity with MHS GENESIS (Cerner), military medical operations, clinical workflows within military treatment facilities (MTFs), and DoD clinical research governance. The CRC ensures operational excellence in studies involving active-duty service members, veterans, and beneficiaries while maintaining the highest standards of data integrity and participant safety.

Clinical Operations

Reports to: Clinical Operations Study Manager

Education

Bachelor’s degree, preferably with a focus in science, public health, healthcare administration, or related field required.

Licensure

N/A

Clinical Experience

N/A

Research Experience

At least 5 years of clinical research experience required, preferably within the DoD, VA, or other US government clinical research settings.

Research Certification

SOCRA/ACRP certification preferred

DOD Site Requirements
  • Ability to obtain and maintain a security clearance per US government requirements.
  • Up to date immunizations.
Core Skills & Experience
  • Strong understanding of clinical research operations, GCP, and human subjects research principles.
  • Ability to perform study procedures with high accuracy and attention to protocol detail.
  • Ability to support multiple studies, priorities and deadlines in a fast-paced research environment.
  • Strong communication skills, professionalism, and ability to collaborate with interdisciplinary teams.
  • Proficiency with Microsoft Office, EDC systems, and remote collaboration tools.
  • Experience within DoD, VA, or other US government healthcare environments is highly desirable.
  • Working knowledge of the Department of Defense Military Health System, including clinical workflows and research oversight processes.
  • Experience with EHR systems such as MHS GENESIS (Cerner) preferred.
Job Responsibilities
  • Coordinate operational aspects of clinical research projects across assigned study sites, including military treatment facilities.
  • Support the development, maintenance, and review of regulatory documents (e.g., ICFs, protocol amendments, IRB submissions).
  • Assist in participant screening, eligibility verification, recruitment tracking, and scheduling in alignment with protocol requirements.
  • Serve as a point of contact for site personnel, investigators, and DoD clinical research offices.
  • Ensure all study activities meet GCP, FDA, ICH, and DoD Human Research Protection Program (HRPP) requirements.
  • Support data abstraction from MHS systems and ensure accurate, timely entry into EDC and study databases.
  • Monitor protocol adherence and elevate deviations or safety concerns appropriately.
  • Prepare for site visits, audits, and monitoring activities; support follow-up and documentation.
  • Collaborate with cross-functional stakeholders, including biostatistics, data science, and clinical operations teams.
  • Maintain complete study records, logs, and documentation in compliance with Azimuth SOPs and DoD regulatory frameworks.
  • Schedule flexibility to support calls related to patients that may occur early in the morning or late in the evening as well as potentially on the weekends.
  • Contribute to process improvement and quality initiatives across Azimuth’s research operations.
  • Ability to perform protocol procedures as needed (e.g. phlebotomy, ECGs, biological specimen collection).
  • Attend study and staff meetings as required.
  • Assist with regulatory submissions as needed.
Extent of Travel

Up to 25%, including travel to military treatment facilities and partner sites.

Management or Individual Contributor

Individual Contributor

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