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Crc Global Jobs (NOW HIRING)

CRC Group

Tax Senior Manager

Charlotte, NC · On-site

The Tax Senior Manager will report to the Head of Global Tax and work closely with various ... At CRC Group, we're committed to supporting every aspect of teammates' well-being - physical ...

Amgen Inc. (IR)

$144 - $195/hr

First Line Launch Strategy and Readiness Support global launch strategy and readiness workstreams across anticipated first line NSCLC and CRC indications. Help shape strategies that address the ...

New

CRC Group

Equity Administration Manager

Charlotte, NC · On-site

$110 - $140/hr

CRC - Charlotte, NC 600 S. Tryon St.time type: Full timeposted on: Posted Yesterdayjob requisition ... Ability to interpret and apply SEC, IRS, and global compliance guidelines.* Excellent communication ...

CRC Group

Tax Senior Manager

Charlotte, NC · On-site

$140 - $195/hr

The Tax Senior Manager will report to the Head of Global Tax and work closely with various ... CRC Group is a Drug Free Workplace.*** #J-18808-Ljbffr

CRC Group

$140 - $195/hr

The Tax Senior Manager will report to the Head of Global Tax and work closely with various ... CRC Group is a Drug Free Workplace.*** #J-18808-Ljbffr

Revolution Medicines

Director, Global Marketing

The Directors of Global Marketing will support the pancreatic, lung, and/or CRC cancer teams and will help shape and enable Revolution Medicines' global go-to-market and launch plans across key ...

Revolution Medicines

Director, Global Marketing

The Directors of Global Marketing will support the pancreatic, lung, and/or CRC cancer teams and will help shape and enable Revolution Medicines' global go-to-market and launch plans across key ...

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Crc Global information

What is a CRC Global?

A CRC Global typically refers to a Clinical Research Coordinator (CRC) who works on global or international clinical trials. This role involves managing and overseeing clinical studies across multiple countries, ensuring compliance with international regulations, and coordinating with diverse research teams. CRC Globals are responsible for patient recruitment, data collection, and maintaining study documentation while navigating the challenges of cross-cultural communication and varying regulatory requirements. Their work is essential for the success of global pharmaceutical and medical research projects.

What are some common challenges faced by professionals working at CRC Global, and how can new employees prepare for them?

At CRC Global, professionals often operate in fast-paced, collaborative environments where they must manage multiple projects and clients simultaneously. New employees may find it challenging to quickly adapt to evolving client needs and maintain effective communication across cross-functional teams. To succeed, it's helpful to develop strong organizational skills, stay proactive in seeking feedback, and be open to learning from experienced colleagues. Embracing the company's culture of teamwork and continuous improvement can also help new hires navigate these challenges successfully.

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, you need a solid background in clinical research, medical terminology, and regulatory compliance, often supported by a degree in a health-related field and certifications like CCRC or CCRP. Familiarity with electronic data capture systems, clinical trial management software, and Good Clinical Practice (GCP) guidelines is essential. Excellent organizational skills, attention to detail, and strong interpersonal communication help you manage studies and interact with participants and research teams. These competencies ensure that clinical trials are conducted ethically, accurately, and efficiently, safeguarding participant safety and research integrity.

What is the difference between Crc Global vs Crc Technician?

AspectCrc GlobalCrc Technician
CertificationsTypically requires industry-specific certifications, such as CRC certification or related credentialsRequires similar certifications, often including CRC certification and technical training
Work EnvironmentOften involves project management, client interaction, and overseeing multiple sitesPrimarily hands-on technical work at specific sites or facilities
Employer & Industry UsageUsed by companies providing comprehensive CRC services, including consulting and project managementCommonly employed by service providers performing technical CRC tasks

The main difference is that Crc Global typically refers to a broader, managerial, or consulting role overseeing CRC projects, while Crc Technician focuses on technical, hands-on tasks. Both roles require similar certifications, but their responsibilities and work environments differ significantly.

What cities are hiring for Crc Global jobs?

Cities with the most Crc Global job openings:

What states have the most Crc Global jobs?

States with the most job openings for Crc Global jobs include:

What job categories do people searching Crc Global jobs look for?

The top searched job categories for Crc Global jobs are:

Crc Global jobs near you
Infographic showing various Crc Global job openings in the United States as of August 2026, with employment types broken down into 84% Full Time, 11% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 4% Hybrid, and 9% 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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