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Clinical Research Coordinator with a Medical Background

13 hours ago


Cambridge ON NR V, Canada Cardiology Office Full time

Cambridge Cardiac Care Centre seeks full time IN CLINIC Clinical Research Coordinator with strong Cardiology experience with a medical background research based experience. Our Centre has over 30 yrs of experience in Clinical Research. The candidate must have the ability to multi-task, problem solve, prioritize, demonstrate proficiency in computer skills, self-directed, independent work. Demonstrated excellence in communication, organization, & collaboration.

Job Entails:

Conducting Phase IIb, III, and Phase IV trials according to study protocol

  • Conduct clinical research studies in compliance with the study protocol, Good Clinical Practice (GCP), and CHCT Research SOPs.
  • Screening patients for inclusion and exclusion criteria
  • Conduct Patient visits as per protocol, assess Adverse events
  • Data collection & Entering data into electronic case report forms
  • Collecting vital signs, performing ECGs
  • Proficiently perform phlebotomy to collect patient samples, handle biological sample processing
  • Lab specimen preparation, processing, and shipment
  • Manage adverse and serious adverse events, timely reporting
  • Participate in monitoring visits, investigator meetings, site initiation visits, closeout visits, and audits
  • Travel to attend research and investigator meetings as required
  • Answer health related questions under the supervision of a cardiologist

Requirements:

  • Only applicants currently residing in Canada, able to work FULL TIME, in Ontario will be considered
  • Good Clinical Practice (GCP) Certification required
  • Medical Degree working in hospitals or Clinic setting for 2-3 yrs
  • Certifications from SOCRA (Society of Clinical Research Associates) or ACRP (Association of Clinical Research Professionals) are highly preferred.
  • Clinical research experience x 2 yrs
  • Phlebotomy certification is required.
  • Maintain regulatory documentation and study-specific logs
  • Ability to think critically, solve situations based on protocols and algorithms
  • Excellent communication skills - verbal and and written for interaction with patients, sponsors, and research team
  • Work independently & with Research team
  • CPR/First AID, WHIMS, IATA, Division 5 Training (required)
  • Excellent computer skills: Competency in clinical trial management systems (CTMS) and MS Office Suite (Word, Excel, PowerPoint).
  • Valid Canadian Passport - Ability to travel to the US and Canada for investigator meetings

Hours: In Clinic - Monday to Fri 8:30-5pm (rarely Saturdays or beyond business hours if required by study protocol), Full Time, Permanent

Competitive Wages

Benefits:

  • Dental care
  • Extended health care

Application question(s):

  • Outline your clinical trial experience
  • Describe your experience with patient history taking
  • Provide examples of your organizational skills

Job Type: Full-time

Pay: $35.00-$40.00 per hour

Benefits:

  • Dental care
  • Extended health care
  • On-site parking

Ability to commute/relocate:

  • Cambridge, ON N1R 6V6: reliably commute or plan to relocate before starting work (preferred)

Application question(s):

  • Are you able to work in Clinic, Full time hours?

Education:

  • Doctoral Degree (preferred)

Experience:

  • Clinical Research : 2 years (required)

Work Location: In person