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First seen by our source: 2 hours ago

Clinical Assistant Intern

@ Cliantha Research Limited

Mississauga, Ontario

Apply now
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Overview

Cliantha Research Limited is offering a three-month unpaid clinical assistant internship supporting clinical research studies. The role involves taking vital signs, processing samples, performing in-house screening tests and monitoring study subjects during confinement.

Responsibilities:

  • Take vital signs and body measurements from study subjects
  • Process blood and urine samples per protocol
  • Run in-house screening diagnostics
  • Monitor subjects during confinement periods
  • Prepare study materials and clinic supplies

Requirements summary:

  • Willingness to take part in training sessions
  • Safe working practices
  • Ability to follow protocols and SOPs

Tools & skills

Source and dates

Source type not verified · apify-linkedin

Employer posting date
Not provided
First seen by our source
2026-11-15
Source record updated
2026-11-15

These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.

Job details

SeniorityEntry level
DepartmentAllied health
Travelair: none · ground: none
Work settingHospital or clinic, Laboratory
PositionSitting and standing
Physical demandsphysical low · computer low

Summary and details written by AI from the posting; the employer’s posting is the authority.

Cliantha Research Limited

FieldValue
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Job description

Please note that this is a three month unpaid internship

Job Description / Roles and Responsibilities for Job Title:

· Obtaining Vital signs (blood pressure, temperature, pulse oximetry, respiration rate)

· Processing of blood and urine samples as per protocol requirements

· Perform in-house screening diagnostics such as Drug Screen panels, pregnancy tests, cotinine tests, alcohol breathalyzer tests, etc.

· Obtaining subject’s height, weight, elbow breadth, frame size and body mass index

· Study related tasks such as meals (distribution, collection and monitoring), subject assembly, check in procedures, property room, etc.

· Monitor subjects during in-house confinement periods for protocol and SOP requirement such as physical restrictions, water restrictions, meals, fluid intake/output, etc.

· Preparation of study related materials, such as labelling of study tubes, preparation of clipboards, ensuring clinic is prepared with supplies required.

· Performing Archiving and Data Entry as required

· Participate in training sessions.

· Work in a safe manner that does not endanger yourself or your co-workers.

· Execute other duties as may be required by their manager and other members of Management team as training and experience allow.

· Any Additional responsibility given by Head of the Department / Management

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