Clinical Study Coordinator/Research Nurse

at  Clinical Research of Ontario

Scarborough, ON M1S 4T7, Canada -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate18 Apr, 2025Not Specified19 Jan, 20253 year(s) or aboveMedical Records,Data Systems,Clinical Research,LicensureNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

CLINICAL STUDY COORDINATOR/RESEARCH NURSE JOB DESCRIPTION

Job Title: Clinical Research Nurse
Employment Type: Part-time

QUALIFICATIONS:EDUCATION AND LICENSURE

  • Asses: Registered Nurse (RN) license (current and in good standing).
  • Required: Bachelor’s degree in a Science related field

EXPERIENCE

  • Previous experience as a Clinical Research Coordinator is a MUST
  • Research Nurse is an ASSET
  • At least 3-5 years of experience in clinical research or related healthcare roles is a MUST
  • Experience with investigational drug administration and clinical trial procedures is a MUST

KNOWLEDGE AND SKILLS

  • Familiarity with GCP, FDA, ICH, and other clinical research regulations.
  • Proficiency in electronic medical records (EMRs) and clinical research data systems.
  • Strong communication, organizational, and problem-solving skills.
  • Ability to manage multiple tasks and prioritize effectively.
    Job Type: Part-time
    Pay: From $45.00 per hour
    Expected hours: 15 – 30 per week

Benefits:

  • On-site parking

Schedule:

  • Monday to Friday

Education:

  • Bachelor’s Degree (required)

Work Location: In person
Expected start date: 2025-02-1

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities:

  • Perform clinical assessments and monitor the health of participants throughout the study.
  • Administer investigational products (e.g., medications, vaccines) according to study protocols.
  • Collect and process biological specimens, such as blood, urine, or saliva, for analysis.
  • Monitor participants for adverse events and report findings to the PI and study sponsors.


REQUIREMENT SUMMARY

Min:3.0Max:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

A science related field

Proficient

1

Scarborough, ON M1S 4T7, Canada