Full-Time APP Sub-Investigator Role in Dallas, Texas

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: 

• Master’s 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 participant’s 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.

M3 Wake Research, Inc., one of the largest independent clinical research site services companies in North America with more than 18 owned and managed research sites across seven states in the US and continues to grow.