Clinical Research Intern

IconRaleigh, NC
128d

About The Position

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. This role is with Accellacare, part of ICON's clinical research network, where you'll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.

Responsibilities

  • Promoting the mission of Accellacare to function as an Integrated Site Network providing unparalleled service to our clinical trial partners.
  • Actively striving to meet and exceed action items as discussed quarterly with direct supervisor.
  • Actively recruiting and selling our service to suitable patient participants and sponsor representatives.
  • Assisting Clinical Research Coordinators as they perform tasks required to coordinate and complete a study according to the protocol.
  • Assisting Clinical Research Coordinators with patient visits, documentation, CRF completion, data queries and monitor visits.
  • Performing clinical requirements of study protocols, i.e., lab work (phlebotomy and processing), blood pressure, electrocardiograms, pulmonary function testing, urine/serum pregnancy testing, strep throat screening, or any procedure necessary for the protocol as ordered by the investigator or coordinator.
  • Assisting in the laboratory or with other laboratory duties such as performing quality assurance review, restocking of supplies and processing of specimens.
  • Performing consult visits as needed.
  • Helping maintain accuracy with the patient database, including data entry and updating existing patient files.
  • Assisting the Clinical Research Coordinator or other staff members with creating and copying patient files for study closeout procedures.
  • Typing memos, letters, phone screeners, progress notes and various documents.
  • Filing labs and correspondence.
  • Performing various errands to pick up dry ice, supplies, samples, physician signatures and storage boxes, etc.
  • Assisting Clinical Research Coordinators or other staff members as determined by the needs and priorities of the research organization, and as time and abilities permit.
  • Assisting with answering the telephones, making appointment reminder calls and initial phone screening.

Benefits

  • Various annual leave entitlements.
  • A range of health insurance offerings to suit you and your family's needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being.
  • Life assurance.
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
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