QCR Network
Clinical Research Coordinator at QCR Network Detroit, MI
QCR Network, Detroit, Michigan, United States, 48228
Overview
Clinical Research Coordinator job at QCR Network. Detroit, MI.
Clinical Research Coordinator
Location: Detroit, MI (On-Site)
Company: NRST–Detroit
Come Join a Growing Company!
Do you have what it takes to be a great Clinical Research Coordinator?
NRST–Detroit is seeking an experienced Clinical Research Coordinator (CRC) to join our expanding research team. This role offers the opportunity to work at a top-ranked research company and contribute to advancing medicine while working directly with patients and a multi-disciplinary team.
Please Note: This is not a remote position.
Position Highlights As a Clinical Research Coordinator, you will work under the guidance of the Principal Investigator to ensure clinical trials are conducted according to Good Clinical Practice, study protocols, and regulatory guidelines. You’ll play a critical role in managing day-to-day study activities, coordinating with study teams, and ensuring high-quality data collection.
Responsibilities
Study Management:Oversee daily trial operations, coordinate study visits, manage subject schedules, and maintain accurate documentation.
Participant Recruitment & Enrollment:Identify, screen, and consent eligible participants while ensuring ethical and accurate enrollment.
Data Collection & Management:Perform study assessments, collect and record data, and maintain confidentiality and integrity of all records.
Regulatory Compliance:Ensure adherence to IRB, FDA, and sponsor requirements; maintain regulatory documents and informed consent processes.
Study Coordination & Communication:Act as the main liaison between participants, investigators, sponsors, and vendors.
Adverse Event Monitoring:Track, document, and report adverse events promptly; ensure participant safety.
Quality Assurance:Perform source data verification, assist with audits, and support data validation efforts.
Clinical Tasks:Perform phlebotomy, obtain vitals, and assist with protocol-related clinical procedures.
Qualifications
Required:
Minimum 2 years of experience inclinical research
Background asMA, LPN, RN, CNA, or Medical Scribe
Strong interpersonal skills and ability to build positive relationships
Proficiency withMS Office Suite(Outlook, Word, Excel, PowerPoint, SharePoint)
Familiarity with clinical trial management systems and TMF filing practices
Knowledge of study drug background and trial requirements
High ethical standards, professionalism, and strong attention to detail
Phlebotomy experience
Prior experience with regulatory submissions and site audits
Strong organizational skills and ability to multitask in a fast-paced environment
Additional Requirements
Must be located in theDetroit, MI area(no relocation stipend provided)
Ability to travel occasionally for investigator meetings or audits
Passion for patient care and research advancement
Physical requirements include sitting for long periods, using a computer, lifting up to 15 lbs, and performing clinical procedures
Why Join Us? At NRST–Detroit, we are committed to conducting cutting-edge clinical trials that make a difference in patients’ lives. We value teamwork, professional growth, and high ethical standards. If you’re ready to bring your skills to a growing company and contribute to meaningful research, we’d love to hear from you!
How to Apply Send your resume and cover letter to mercedes.livingston@qcromaha.com with the subject line: Clinical Research Coordinator – Detroit.
#J-18808-Ljbffr
Position Highlights As a Clinical Research Coordinator, you will work under the guidance of the Principal Investigator to ensure clinical trials are conducted according to Good Clinical Practice, study protocols, and regulatory guidelines. You’ll play a critical role in managing day-to-day study activities, coordinating with study teams, and ensuring high-quality data collection.
Responsibilities
Study Management:Oversee daily trial operations, coordinate study visits, manage subject schedules, and maintain accurate documentation.
Participant Recruitment & Enrollment:Identify, screen, and consent eligible participants while ensuring ethical and accurate enrollment.
Data Collection & Management:Perform study assessments, collect and record data, and maintain confidentiality and integrity of all records.
Regulatory Compliance:Ensure adherence to IRB, FDA, and sponsor requirements; maintain regulatory documents and informed consent processes.
Study Coordination & Communication:Act as the main liaison between participants, investigators, sponsors, and vendors.
Adverse Event Monitoring:Track, document, and report adverse events promptly; ensure participant safety.
Quality Assurance:Perform source data verification, assist with audits, and support data validation efforts.
Clinical Tasks:Perform phlebotomy, obtain vitals, and assist with protocol-related clinical procedures.
Qualifications
Required:
Minimum 2 years of experience inclinical research
Background asMA, LPN, RN, CNA, or Medical Scribe
Strong interpersonal skills and ability to build positive relationships
Proficiency withMS Office Suite(Outlook, Word, Excel, PowerPoint, SharePoint)
Familiarity with clinical trial management systems and TMF filing practices
Knowledge of study drug background and trial requirements
High ethical standards, professionalism, and strong attention to detail
Phlebotomy experience
Prior experience with regulatory submissions and site audits
Strong organizational skills and ability to multitask in a fast-paced environment
Additional Requirements
Must be located in theDetroit, MI area(no relocation stipend provided)
Ability to travel occasionally for investigator meetings or audits
Passion for patient care and research advancement
Physical requirements include sitting for long periods, using a computer, lifting up to 15 lbs, and performing clinical procedures
Why Join Us? At NRST–Detroit, we are committed to conducting cutting-edge clinical trials that make a difference in patients’ lives. We value teamwork, professional growth, and high ethical standards. If you’re ready to bring your skills to a growing company and contribute to meaningful research, we’d love to hear from you!
How to Apply Send your resume and cover letter to mercedes.livingston@qcromaha.com with the subject line: Clinical Research Coordinator – Detroit.
#J-18808-Ljbffr