What are the responsibilities and job description for the Clinical Research Nurse Practitioner Sub Investigator PRN position at M3USA?
The SubInvestigator provides oversight in medical and clinical issues as requested or required. The SubInvestigator works with the Principal Investigator (PI) to evaluate clinical trials and ensure that all studyrelated procedures are completed in accordance with Good Clinical Practices (GCP). The SubInvestigator performs critical trialrelated procedures and makes important trialrelated decisions when delegated by the PI to do so. SubInvestigator is engaged in the informed consent process and has a significant role in the conduct of research. This position is primarily responsible for the accurate completion of visit procedures and collection of information from study participants according to protocols and for protecting the health safety and welfare of research participants.
Essential Duties and Responsibilities :
Including but not limited to the following :
- Provides participant consultations and education in an in or outpatient setting under the direction of the PI in charge of the clinical trial.
- Conducts studyrelated physical exams and followup visits.
- Reviews and adheres to assigned research study protocols.
- Works with the studyleading PI in evaluation and review of potential study participant eligibility.
- Maintains proper documentation in accordance with GCP.
- Ensures that all clinical activities are carried out in accordance with established research protocols and standards in compliance with all applicable laws regulations policies and procedural requirements.
- Collaborates with multidisciplinary team members.
- Reviews lab results imaging reports and other studyspecific reports.
- Reviews and verifies participant medical history collected by the Wake Research Staff / Clinicians.
- Communicates with the participant as well as the participants partner / informant / caregiver.
- Attend and successfully complete all training programs in a timely manner
- Attend participate in and complete ongoing conference calls webinars required meetings and other professional development opportunities.
- Complete provided rater training Good Clinical Practice (GCP) training and any Sponsor required trainings.
- Conduct participant interviews following specific study protocols FDA GCP ICH and HIPAA Privacy guidelines.
- Maintains knowledge and education of all applicable rules regulations policies laws and guidelines respective to their field and role.
- Support site operations for community outreach and recruiting efforts.
Qualifications : Requirements :
Additional Information :
About M3 :
M3 USA is at the forefront of healthcare innovation offering digital solutions across healthcare life sciences pharmaceuticals and more. Since our inception in 2000 weve seen remarkable growth fueled by our mission to utilize the internet for a healthier world and more efficient healthcare systems.
Our success is anchored in our trusted digital platforms that engage physician communities globally facilitating impactful medical education precise job placement and insightful market research. M3 USA prides itself on a dynamic and innovative work environment where every team member contributes to global health advancements.
Joining M3 USA means being part of a dedicated team striving to make a significant difference in healthcare. We provide a unique opportunity for you to be at the cutting edge of healthcare innovation shaping the future in a meaningful career. Embrace the chance to drive change with M3 USA.
Compensation for this role is $70.00 / hr to $85.00 / hr.
All your information will be kept confidential according to EEO guidelines.
LIOnsite
LIJD1
Remote Work : Employment Type :
Contract
Salary : $70 - $85
