Unfortunately, this job posting is expired.
Don't worry, we can still help! Below, please find related information to help you with your job search.
Some similar recruitments
Clinical Scientist Jobs
Recruited by Kelly 9 months ago Address Philadelphia, PA, United States
Dms Clinical Coordinator Jobs
Recruited by Hi-Quality Recruits 9 months ago Address Reading, PA, United States
Clinical Coordinator - Psychotherapy
Recruited by St. Luke's University Health Network 9 months ago Address Allentown, PA, United States
Clinical Data Coordinator, Oncology
Recruited by ConcertAI 10 months ago Address Greater Philadelphia, United States
Data Scientist Jobs
Recruited by Croptix 1 year ago Address State College, PA, United States
Jr. Data Scientist Jobs
Recruited by Comcast 1 year ago Address , Philadelphia, 19103, Pa $74,853 - $175,437 a year
Data Scientist Jobs
Recruited by Cadent 1 year ago Address , Philadelphia, 19102, Pa

Clinical Data Coordinator Jobs

Company

Medix™

Address Pennsylvania, United States
Employment type FULL_TIME
Salary
Category Hospitals and Health Care
Expires 2023-09-22
Posted at 8 months ago
Job Description

FULLY REMOTE | CLINICAL DATA COORDINATOR | EAST COAST | APPLY TODAY


Job Summary

Under the direction of the Clinical Research Manager, the research associate will work with physicians, nurses and allied health professionals to facilitate clinical research trials and independently execute job functions related to protocol management.


Duties and Responsibilities

  • Assists the research team with the screening process and ensures that subject’s records, archival tissue, radiology tests, lab work results, etc. are obtained prior to subject entry into a study.
  • Assists with monitoring visits and coordinate data collection including data locks.
  • Assists in the consent process for patients on minimal risk/non-therapeutic trials.
  • Responsible for lab kit inventory, preparation and tissue requests.
  • Responsible for prompt and accurate data entry for protocols, including Serious Adverse Events.
  • Performs query resolution.
  • Performs study specified electrocardiograms.
  • Works with research team in managing the visits of active and follow up subjects on research protocols.
  • Attends study related biopsies and transports tissue samples for processing.
  • Assists in the coordination of initiation, site evaluation, monitoring visits, and audits required by the sponsor.
  • Maintains patient tracking spreadsheets to ensure data entry requirements are met.
  • Demonstrates industry accepted good documentation and clinical practices during the conduct of research to collect quality data, in compliance with institutional, and statutory guidelines.
  • Processes study specific data collection documents into case report forms.