Full-Time APP Sub-Investigator Role in Dallas, Texas at CS Wake Research

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.