Medical Screener

Pharma Medica Research Inc.

ON, ON

JOB DETAILS
LOCATION
ON, ON
POSTED
30+ days ago

Description

Pharma Medica Research is a full service contract research organization specialized in conducting early phase clinical trials in healthy volunteers, special and patient populations. Currently we are looking for a part-time Medical Screener to join our team our Scarborough team!

The Medical Screener ensures that potential subjects meet the protocol requirements to ensure a full panel is obtained for each study at Pharma Medica Research Inc. (PMRI). This position reports to the Supervisor, Screening.

Responsibilities:

  • Read, understand, and be familiar with study protocols.
  • Communicate clearly and effectively with prospective subjects and other screening staff.
  • Conduct initial interview with prospective subjects and record subjects' medical history.
  • Obtain Informed Consent from prospective subjects by providing clear explanation of informed consent and answering questions or concerns of potential participants.
  • Perform screening procedures such as but not limited to: blood sample collection, sample processing and storage, vital signs, ECGs, etc., according to the study protocol and/or SOP requirements.
  • Procure and/or process biological samples as required to conduct a clinical study.
  • Perform general clinical duties to prepare for the clinical study (i.e. tube labeling, set up bleeding stations, etc).
  • Perform general cleaning duties (i.e. decontaminate workstations and equipment such as centrifuges and fridges).
  • Properly complete documentation of clinical activities according to GCP, SOP guidelines, and/or FDA/TPD regulations.
  • Participate regularly in PMRI training programs including GCP, SOP training and PMRI in-house training modules test.
  • Achieve 80% or greater in all PMRI training evaluations including GCP, SOP tests and PMRI in-house training module test.
  • Follow Joint Health and Safety rules and regulations at all times
  • Perform any tasks required by the Screening Group Leader/Study Coordinator deemed necessary to conduct a clinical study.
  • Other duties as required.

Skills and Qualifications:

  • Three years community college or university degree.
  • Completion of recognized Phlebotomy/ECG program. Minimum amount of practical work experience
  • Must be familiar with medical terminology or nursing background.
  • 1 year working experience in a medical environment (clinic)
  • 1 year CRO experience or equivalent
  • Excellent verbal and written English communication skills.
  • Excellent interpersonal skills.
  • Ability to work both independently and as a team member.

If you meet the needs of this position, apply today!!