Avery Partners
Job DescriptionJob Description
Job Title:
Clinical Research Nurse Coordinator
Like the look of this opportunity Make sure to apply fast, as a high volume of applications is expected Scroll down to read the complete job description. Reports To:
Director of Research Schedule:
Full-Time | Monday–Friday Position Overview: We are seeking an experienced Clinical Research Nurse Coordinator to support a growing clinical research program within a specialized outpatient setting. This role is ideal for a registered nurse with hands-on IV infusion experience and a strong background in clinical trials. The coordinator will play a key role across the full lifecycle of multiple studies, ensuring compliance with regulatory requirements while supporting participant safety and data integrity. This position involves working with both FDA-approved and investigational therapies and managing approximately 3–5 active research projects at a time. Key Responsibilities: Collaborate closely with the Principal Investigator to conduct clinical studies in accordance with FDA regulations, sponsor requirements, and Good Clinical Practice (GCP) guidelines
Ensure the safety, rights, and well-being of all research participants
Independently organize and manage research workflows and study documentation
Review protocols and prepare sites for study initiation
Screen and recruit eligible participants based on inclusion and exclusion criteria
Coordinate and conduct scheduled study visits per protocol
Lead and document the informed consent process, addressing participant questions under PI guidance
Maintain accurate and complete source documentation, regulatory binders, and study logs
Collect, abstract, and enter study data into case report forms (CRFs)
Identify, document, and report adverse events, serious adverse events, protocol deviations, and unanticipated problems in accordance with federal and IRB guidelines
Perform study-related clinical assessments such as vital signs, EKGs, lab draws, and IV infusions
Manage investigational product accountability, including receipt, storage, dispensing, and returns
Serve as the primary point of contact during sponsor interactions including site initiation, monitoring, audits, and close-out visits
Assist with training and mentoring research and clinic staff as needed
Complete additional duties as assigned to support research operations
Qualifications: Bachelor’s degree required
Minimum of 3 years of clinical research experience
Strong knowledge of GCP, human subject protection, and FDA clinical research regulations
Experience conducting infusion-based or interventional studies preferred
Certifications (Required or Preferred): RN, CPR
GCP certification
IATA and other research-related certifications preferred
Certified Clinical Research Coordinator (CCRC) strongly preferred
Company DescriptionAvery Partners collaborates with businesses all over the US to help streamline their hiring processes. xsgimln Company DescriptionAvery Partners collaborates with businesses all over the US to help streamline their hiring processes.
Job Title:
Clinical Research Nurse Coordinator
Like the look of this opportunity Make sure to apply fast, as a high volume of applications is expected Scroll down to read the complete job description. Reports To:
Director of Research Schedule:
Full-Time | Monday–Friday Position Overview: We are seeking an experienced Clinical Research Nurse Coordinator to support a growing clinical research program within a specialized outpatient setting. This role is ideal for a registered nurse with hands-on IV infusion experience and a strong background in clinical trials. The coordinator will play a key role across the full lifecycle of multiple studies, ensuring compliance with regulatory requirements while supporting participant safety and data integrity. This position involves working with both FDA-approved and investigational therapies and managing approximately 3–5 active research projects at a time. Key Responsibilities: Collaborate closely with the Principal Investigator to conduct clinical studies in accordance with FDA regulations, sponsor requirements, and Good Clinical Practice (GCP) guidelines
Ensure the safety, rights, and well-being of all research participants
Independently organize and manage research workflows and study documentation
Review protocols and prepare sites for study initiation
Screen and recruit eligible participants based on inclusion and exclusion criteria
Coordinate and conduct scheduled study visits per protocol
Lead and document the informed consent process, addressing participant questions under PI guidance
Maintain accurate and complete source documentation, regulatory binders, and study logs
Collect, abstract, and enter study data into case report forms (CRFs)
Identify, document, and report adverse events, serious adverse events, protocol deviations, and unanticipated problems in accordance with federal and IRB guidelines
Perform study-related clinical assessments such as vital signs, EKGs, lab draws, and IV infusions
Manage investigational product accountability, including receipt, storage, dispensing, and returns
Serve as the primary point of contact during sponsor interactions including site initiation, monitoring, audits, and close-out visits
Assist with training and mentoring research and clinic staff as needed
Complete additional duties as assigned to support research operations
Qualifications: Bachelor’s degree required
Minimum of 3 years of clinical research experience
Strong knowledge of GCP, human subject protection, and FDA clinical research regulations
Experience conducting infusion-based or interventional studies preferred
Certifications (Required or Preferred): RN, CPR
GCP certification
IATA and other research-related certifications preferred
Certified Clinical Research Coordinator (CCRC) strongly preferred
Company DescriptionAvery Partners collaborates with businesses all over the US to help streamline their hiring processes. xsgimln Company DescriptionAvery Partners collaborates with businesses all over the US to help streamline their hiring processes.