Clinical Research Nurse II

The Clinical Research Coordinator II Nurse (CRC II RN) will be responsible for coordinating advanced clinical research projects proficiently with supervision, to collect, process, store and ship research specimens proficiently. Capable of independent chart review and data entry. May meet with clinical monitor to support data verification. May independently resolve data queries for review and approval of principal investigator. Functions independently, and is able to identify situations where additional support is necessary.

The Clinical Research Coordinator II Nurse (CRC II RN) will be responsible for coordinating advanced clinical research projects proficiently with supervision, to collect, process, store and ship research specimens proficiently. Capable of independent chart review and data entry.  May meet with clinical monitor to support data verification.  May independently resolve data queries for review and approval of principal investigator.   Functions independently, and is able to identify situations where additional support is necessary.  Independently able to access regulations governing the protection of human subjects- IRB, FDA, OHRP, GCP/ICH and HIPAA guidelines and apply regulations in practice. The CRC II RN will assure that the integrity and quality of the clinical research trial data is maintained in accordance with all Meharry Medical College, IRB, and PCIR policies and standard operating procedures.  Responds to inquiries on specific tasks of study projects, ensures support of compliance with protocols and overall objectives, and performs study-related procedures of clinical research under the supervision of the Associate Director and Medical Director.  

Daily Operations

• Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and nurses.
• Maintain required records of study activity including case report forms, consenting research subjects, or regulatory forms.
• Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiogram
• Direct the requisition, collection, labeling, storage, or shipment of specimens.
• Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices. Schedules subjects for appointments and procedures as required by study protocols

                                                                                                                                                    

Required Skills

• Must possess a proficient working knowledge of advanced clinical research support practice.
• Must be proficient with personal computer.
• Ability to utilize keen judgment in evaluating information.
• Ability to numerically and accurately enter and calculate test results in an electronic database.
• Ability to work in a stressful environment.
• Must be team oriented

Required Education and Experience

• Graduated from an accredited discipline specific program and licensed as a registered nurse in the state of Tennessee.  60 months experience in a patient care setting required (clinical research experience preferred).