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Company

Headlands Research

Address Escondido, CA, United States
Employment type FULL_TIME
Salary
Category Research Services
Expires 2023-09-22
Posted at 8 months ago
Job Description
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 Research Assistant to organize the collection of data, documentation, and record-keeping activities pertaining to clinical research studies. This person will promote Good Clinical Practices in the conduct of clinical investigations by possessing an in-depth knowledge of FDA regulations and human subject protection, thus, ensuring compliance with protocol and regulatory requirements.


Position Type Full-Time


Pay Range $18-$20/hr


Location Escondido, CA


Travel 0%


Work Schedule Mondays through Fridays, 700am to 400pm
  • Or reasonable combination of the above
  • Weekly temperature report printing and filing
  • Attends study teleconferences and/or meetings
  • Assists with all study-related tasks from start to finish for
  • Files in regulatory binder
  • Monitors temperature monitoring system for temperature acceptability ranges
  • Performs laboratory equipment maintenance
  • BLS or CPR required
  • Completes data entry, CRF’s, electronic data
  • High complexity/demand 1 enrolling study and 1 ongoing study
  • Performs delegated duties vital signs, study questionnaires, ECG’s
  • Low to medium complexity/demand 1 enrolling study and 2 ongoing studies
  • Coordinates shipment of biological samples
  • Has working knowledge of laboratory equipment including centrifuges, scales, hematocrits, A1c, and YSIs
  • Addresses electronic data capture (EDC) queries under guidance of the study coordinator
  • Collects, processes, and assists in the compilation and verification of research data, sample, and/or specimens, following strict protocol and detailed instructions.
  • Becomes familiar with study protocols
  • Collects and processes blood samples and other biological samples
  • Prepares source documents and study binder for subject visits
  • Schedules/confirms subject appointments
  • Medical Assistant certification preferred
  • Basic computer skills, including Microsoft Office suite (including MS Project, Excel, and PowerPoint)
  • Excellent communication, interpersonal skills, including problem solving