What are the responsibilities and job description for the Sub-Investigator / Nurse Practitioner position at Joulé?
Job Title : Nurse Practitioner / Sub-Investigator
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Memphis, TN
Full time, direct hire with client company
Growing Clinical Research Team needs a NP / Sub Investigator to Join the team! Please apply if you’d like to be a part of their groundbreaking research.
Provide leadership to and management of all non-MD clinical personnel congruent with the philosophy and mission. Promote good clinical practices in the conduct of clinical investigations by possessing an in-depth knowledge of federal regulations and guidelines for the enrollment and maintenance of subjects in clinical trials, and by collecting, recording and maintaining source and sponsor documentation.
Primary Responsibilities :
1. Clinical Leadership
2. Staff Management
3. Visit Volume
4. Project Management
5. Education & Training
6. Patient Satisfaction
7. Physician Relations
8. Trial Recruitment
Specific Responsibilities : Ongoing communication with Lead CRC and Principal Investigators to maintain a professional, productive and fun team-oriented culture
Set and maintain the tone for the clinical goals we want to achieve, both internally and with our sponsors
Interface with sponsors as appropriate for the successful management of all clinical trials
Training and development of staff emphasizing both diagnostic and trial conduct acumen including quality, efficiency, and sponsor relations
Serve as Sub I on all trials
Assist with all community related sales, networking, conferences and other activities to ensure the offices’ integration in the medical community and to obtain patient / subject referrals into studies
Assist Administrative Director with managing the HR aspects of the entire office
Manage clinical flow so the day runs smoothly and staff remain caught up
Manage triage productivity with the assistance of the Administrative Director
Keep workload for clinical team manageable and evenly distributed; assess, on an ongoing basis, individual needs that fit the goals and objectives of the team
Ongoing problem solving of all clinic functions including patient scheduling, patient management, laboratory services, etc.
Assist Principal Investigators with identifying trends for patient screen fails, drops, retention, placebo response, etc. and work on improving deficiencies with clinical team
Under the direction of the PI’s, with the assistance of the Administrative Director, lead the initial trial feasibility process to ensure protocols are properly selected and managed for both patients and sponsors
Work with the Regulatory / QA staff to ensure timely implementation of protocols and procedures and maintenance of high quality and integrity
Ensure flow of communication, including telephone conferences, between patients, study staff, referral sources, sponsor and / or CROs, monitors, auditors and any marketing groups hired by the sponsors
Thorough adaptation to any assigned studies through reading protocols, attending investigator meetings and start-up meetings, and orienting with other Principal Investigators.
Perform clinical tasks, as required per protocol, including physicals, psych evals, review AE’s and ECG’s, psychometric and non-psychometric testing, vital signs, height and weight, ECG, phlebotomy, specimen packaging, etc.
Dispense and maintain, as required, accurate records of study medication.
Physical / Mental Abilities and Position Requirements : Learn and support the mission and goals of the program
Proficiency in utilizing various rating scales, and maintenance of inter-rater reliability with other clinicians
Ability to communicate professionally and courteously
