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Ccrp Jobs in Michigan (NOW HIRING)

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Ccrp information

See Michigan salary details

$19.2K

$47.8K

$70.2K

How much do ccrp jobs pay per year?

As of Aug 27, 2026, the average yearly pay for ccrp in Michigan is $47,810.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,400.00 and $54,500.00 per year, depending on experience, location, and employer.

What is a ccrp?

CCRP stands for Certified Clinical Research Professional. These professionals are credentialed by the Society of Clinical Research Associates (SOCRA) after meeting specific education and experience requirements and passing a certification exam. CCRPs play a vital role in clinical research by ensuring that studies are conducted ethically, safely, and in compliance with regulatory standards. Their responsibilities often include managing clinical trials, adhering to protocols, and maintaining high-quality data collection. Becoming a CCRP demonstrates expertise and commitment to excellence in the field of clinical research.

What are the key skills and qualifications needed to thrive as a clinical research professional (CCRP)?

To thrive as a Clinical Research Professional (CCRP), you need a solid understanding of clinical trial protocols, regulatory compliance, and data management, typically backed by a degree in life sciences and CCRP certification. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and regulatory submission platforms is essential. Attention to detail, ethical judgment, and strong organizational and communication skills distinguish top performers in this role. These competencies ensure clinical trials are conducted ethically, efficiently, and in accordance with regulatory standards.

What are some common challenges faced by clinical research coordinators (CCRCs) when managing multiple clinical trials simultaneously?

Clinical Research Coordinators often juggle several studies at once, which can present challenges such as balancing competing deadlines, ensuring compliance with various study protocols, and maintaining accurate documentation. Effective time management and strong organizational skills are crucial to prioritize tasks and prevent errors. Additionally, CCRCs frequently coordinate with investigators, sponsors, and regulatory bodies, so clear communication and adaptability are key to ensuring all trials run smoothly and meet regulatory requirements.

What is the difference between Ccrp vs Clinical Research Coordinator?

AspectCcrpClinical Research Coordinator
CertificationsRequires CCRP certificationMay or may not require CCRP, often has other certifications
Work EnvironmentResearch settings, clinical trialsHospitals, clinics, research sites
Job FocusMonitoring and managing clinical research protocolsParticipant recruitment, data collection, study coordination

The CCRP (Certified Clinical Research Professional) is a certification for professionals involved in clinical research, emphasizing monitoring and compliance. A Clinical Research Coordinator (CRC) is a role that may or may not hold CCRP certification but focuses on coordinating clinical trials and managing participant interactions. While both roles work within the clinical research industry, CCRPs often have specialized certification and focus on oversight, whereas CRCs handle day-to-day trial operations.

How do you become a certified research coordinator?

To become a certified research coordinator, individuals typically need a bachelor's degree in a health-related field and relevant experience in clinical research. They can pursue certification through organizations like the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SOCRA), which require passing an exam and maintaining ongoing education. Certification demonstrates knowledge of Good Clinical Practice (GCP) and regulatory requirements essential for the role.

What are the benefits of CCRP certification?

CCRP (Certified Clinical Research Professional) certification demonstrates a professional's knowledge and competence in clinical research, which can enhance job prospects, credibility, and earning potential. It also signifies adherence to industry standards and may be required or preferred by employers for roles involving clinical trial management and regulatory compliance.
Infographic showing various Ccrp job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $47,810 per year, or $23 per hour.

Research Abstract Analyst III- Full time- Central Abstractor Office- One Ford Place

Henry Ford Health System

Detroit, MI • On-site

Full-time

Posted 12 days ago


Henry Ford Health rating

6.9

Company rating: 6.9 out of 10

Based on 570 frontline employees who took The Breakroom Quiz

458th of 894 rated healthcare providers


Job description

GENERAL SUMMARY:
  • Coordinates data collection team workflow for specified data collection initiatives.
  • Monitors daily productivity in accordance with timeline.
  • Provides for quality assurance activities and coordinates auditing processes with PI.
  • Functions as the liaison between PI/Project Manager and data collection team.
  • Works autonomously using established procedures to interpret and abstract clinical data from the medical record for local, national and international research studies.
  • Abstracts clinical data to satisfy numerous HFHS/HAP compliance and quality initiatives: COE's, P4P, Utilization Review, System Registries, Risk Adjustment, NHSN Infection control, Hospital Acquired Conditions, CMS Core Measures, CMS HCC and Coding validation.
  • Provides coding validation, consulting, and education.

EDUCATION/EXPERIENCE REQUIRED:
  • Associate degree Health Information Management or related field, in addition to maintaining one of the following credentials: RHIT, RHIA, CTR, CCRP, RN.
  • Bachelor's degree required. Five (5) years progressive experience.
  • Must have a thorough knowledge of anatomy, physiology, pathophysiology, disease processes, medical terminology, pharmacology, and coding systems.
  • Working knowledge of Microsoft Office products - Excel, PowerPoint, Word, Access.
  • Familiar with REDCap and Epic.
  • Experience in accessing and utilizing web-based programs, for example, email, internet, vendor-based software as Midas, Quantros, CMS Pharmaceutical and Clinical Trial databases, etc.
  • CERTIFICATIONS/LICENSURES REQUIRED: One of the following credentials: RHIT, RHIA, CTR, CCRP, RN.

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About Henry Ford Health

Sourced by ZipRecruiter

Henry Ford Health provides a full continuum of services from Primary and Preventative care, to Complex and Cpecialty care, Health Insurance, a full suite of home health offerings, Virtual care, Pharmacy, Eye care and other Healthcare retail. It is one of the Nation’s leading Academic Medical Centers, recognized for Clinical excellence in Cancer care, Cardiology and Cardiovascular Surgery, Neurology and Neurosurgery, Orthopedics and Sports medicine, and Multi organ transplants. Consistently ranked among the top five NIH funded institutions in Michigan, Henry Ford Health engages in more than 2,000 research projects annually. Equally committed to educating the next generation of Health Professionals, Henry Ford Health trains more than 4,000 Medical students, Residents and fellows every year across 50+ accredited programs. With more than 33,000 valued team members, Henry Ford Health is also among Michigan’s largest and most Diverse employers, including nearly 6,000 physicians and researchers from the Henry Ford Medical Group, Henry Ford Physician Network and Jackson Health Network.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Detroit, MI, US

Year founded

1915