Overview:
The Headlands Research - AMCR Institute is dedicated to attracting, nurturing, and retaining patients and staff in order to carry out outstanding metabolic research. Our volunteers, sponsors, partners, and staff enjoy working together in an environment of mutual respect that fosters personal growth and optimal health. We passionately believe that the participation of a few in clinical research studies can make a difference to the many that suffer from chronic metabolic conditions. We strive to be the best at what we do and at all times be meticulous in all our practices placing the care, safety, and confidentiality of our volunteers first. Excellence in clinical research, accelerating access to treatments that change lives.
Together with Headlands Research, we are building the best clinical trial company in the world. We’re an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant outreach and participation. Founded in 2018, Headlands Research is in high growth mode; we operate 15 clinical trial sites in the US and Canada and have rapid expansion plans.
The Role
AMCR is looking for a Physician Assistant (PA) or Nurse Practitioner (NP) to coordinate and plan research study-related activities. This person will be responsible for ensuring day-to-day adherence to protocol, regulatory standards, and established policies and practices to deliver high quality and timely study data.
Position Type: PRN/Per Diem/As-Needed
Location: Escondido, CA
Travel: 0%
Work Schedule: Varies; avg of ~12 hours per week
Clinic hours: Mondays through Fridays, 8:00am to 8:00pm
Responsibilities:
Provides patient consultations and education in an outpatient setting under the direction of the physician in charge of the clinical trial
Conducts study-related physical exams and follow-up visits
Reviews and adheres to assigned research study protocol
Works with the study-leading physician in evaluation and review of potential study participants’ eligibility
Maintains proper documentation
Ensures that all clinical activities are carried out in accordance with established research protocol 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
Qualifications:
Graduate of an accredited FNP or PA Masters program required
Current active and unencumbered license to practice as an NP or PA within the state of California required
Minimum of one full year of experience as a fully licensed NP or PA required
Previous experience within the clinical research industry, including a strong working knowledge of the ICH guidelines and FDA, IRB/IEC regulations preferred
Strong computer skills, including Microsoft Word, Excel, and PowerPoint, as well as expertise with multiple EMR/CTM systems
Excellent communication, interpersonal, and leadership skills, including problem solving, team building and coaching.
Ability to work independently and prioritize actively
Permanent