Piper Companies
Piper Companies
is seeking a
Clinical Research Coordinator
for a trusted partner in clinical development located in
Raleigh, North Carolina (NC) . The
Clinical Research Coordinator
would ideally have hands-on
phlebotomy
experience in a
clinical site network environment . This position will sit
on-site
in
Raleigh, NC .
Responsibilities of the Clinical Research Coordinator : Support clinical trials by screening participants, confirming eligibility, and performing phlebotomy and specimen processing per protocol. Ensure data accuracy through timely entry and management of case report forms and study records. Mentor junior staff and uphold protocol compliance and quality standards. Maintain regulatory compliance and assist with study start-up, maintenance, and close-out activities. Adapt to dynamic workflows by managing multiple studies and supporting cross-functional research efforts. Qualifications for the Clinical Research Coordinator :
2-3 years of clinical research coordination experience with strong knowledge of clinical trial protocols and regulatory guidelines (GCP, CFR, HIPAA). Phlebotomy experience is required, along with prior experience as a Medical Assistant, LPN, or RN. Detail-oriented and highly confidential, with a strong commitment to patient privacy and data integrity. Preferred certifications include GCP and Advanced CRC, with demonstrated leadership and interpersonal skills. Compensation for the Clinical Research Coordinator:
Salary Range
: $55,000-$68,000/year Comprehensive Benefits
: Sick leave if required by law, medical, dental, vision, 401K
This job opens for applications on 07/30/2025. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords : Clinical Research, Clinical Research Coordinator, Clinical Operations Coordinator, Clinical Trial Coordinator, Clinical Project Coordinator, Clinical Trials, Research Coordinator, Participant Screening, Case Documentation, Data Integrity, Case Report Forms, Study Records, Staff Training, Protocol Compliance, Regulatory Compliance, GCP, CFR, HIPAA, Study Start-Up, Study Maintenance, Study Close-Out, Multi-Study Management, Cross-Functional Research, Phlebotomy, Medical Assistant, LPN, RN, Patient Privacy, Data Management, Advanced CRC, Leadership, Interpersonal Skills
#LI-GP2 #LI-ONSITE
is seeking a
Clinical Research Coordinator
for a trusted partner in clinical development located in
Raleigh, North Carolina (NC) . The
Clinical Research Coordinator
would ideally have hands-on
phlebotomy
experience in a
clinical site network environment . This position will sit
on-site
in
Raleigh, NC .
Responsibilities of the Clinical Research Coordinator : Support clinical trials by screening participants, confirming eligibility, and performing phlebotomy and specimen processing per protocol. Ensure data accuracy through timely entry and management of case report forms and study records. Mentor junior staff and uphold protocol compliance and quality standards. Maintain regulatory compliance and assist with study start-up, maintenance, and close-out activities. Adapt to dynamic workflows by managing multiple studies and supporting cross-functional research efforts. Qualifications for the Clinical Research Coordinator :
2-3 years of clinical research coordination experience with strong knowledge of clinical trial protocols and regulatory guidelines (GCP, CFR, HIPAA). Phlebotomy experience is required, along with prior experience as a Medical Assistant, LPN, or RN. Detail-oriented and highly confidential, with a strong commitment to patient privacy and data integrity. Preferred certifications include GCP and Advanced CRC, with demonstrated leadership and interpersonal skills. Compensation for the Clinical Research Coordinator:
Salary Range
: $55,000-$68,000/year Comprehensive Benefits
: Sick leave if required by law, medical, dental, vision, 401K
This job opens for applications on 07/30/2025. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords : Clinical Research, Clinical Research Coordinator, Clinical Operations Coordinator, Clinical Trial Coordinator, Clinical Project Coordinator, Clinical Trials, Research Coordinator, Participant Screening, Case Documentation, Data Integrity, Case Report Forms, Study Records, Staff Training, Protocol Compliance, Regulatory Compliance, GCP, CFR, HIPAA, Study Start-Up, Study Maintenance, Study Close-Out, Multi-Study Management, Cross-Functional Research, Phlebotomy, Medical Assistant, LPN, RN, Patient Privacy, Data Management, Advanced CRC, Leadership, Interpersonal Skills
#LI-GP2 #LI-ONSITE