Full-Time APP Sub-Investigator Role in Dallas, Texas
1 month ago
Are you a Nurse Practitioner or Physician Assistant Seeking a Full-Time position in the Dallas area?
M3 Wake Research has an opening for a Sub-Investigator at our Dallas clinic.
Requirements:
- Masters Degree required
- Licensed Advanced Practice Registered Nurse (APRN) successful completion of an accredited through the Commission on Collegiate Nursing Education (CCNE) or the Accreditation Commission for Education in Nursing, Inc. (ACEN) OR
- Physician Assistant (PA-C) successful completion of an accredited Physician Assistant Program recognized by the Accreditation Review Commission on Education for the Physician Assistant (ARC-PA) or its predecessors
- Current license to practice in the state of hire
- No history of license suspension or debarment in any state or by the FDA
- Must have BLS and ACLS certifications; PALS required if pediatric experience needed at site
- Trained in phlebotomy, additional pediatric experience preferred
- Experience in bedside procedures is preferred
- 2 years of clinical practice experience is required
- 2 years of clinical research experience as a sub-investigator is preferred
Duties and Responsibilities:
- Provides participant consultations and education in an in- or out-patient setting under the direction of the PI in charge of the clinical trial.
- Conducts study-related physical exams and follow-up visits.
- Reviews and adheres to assigned research study protocols.
- Works with the study-leading 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 study-specific 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.
If you would be interested in hearing more please contact Scott Plackemeier at spWakeResearch@meddoc.net
M3 Wake Research has a 39 year history of building meaningful relationships with sponsors and CROs, and most importantly, providing excellent care for its patients. There are 26 research sites throughout the USA, offering a dedicated and wholly-owned site network with a centralized, single point of contact for site identification, study implementation and trial management, recruitment and retention, advertising, contracting, and quality control.
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