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Study coordinator • markham on
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Clinic Study Assistant
Pharma Medica Research Inc.Scarborough, ON, Canada- New!
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JL InternationalRichmond Hill, ON, Canada- Toronto, ON (from $ 52,487 to $ 161,540 year)
- Calgary, AB (from $ 87,516 to $ 116,753 year)
- St. John's, NL (from $ 57,641 to $ 116,565 year)
- Old toronto, ON (from $ 58,500 to $ 108,260 year)
- Kitchener, ON (from $ 69,949 to $ 74,880 year)
- Vancouver, BC (from $ 56,229 to $ 73,250 year)
- Edmonton, AB (from $ 62,582 to $ 72,892 year)
- Mississauga, ON (from $ 69,112 to $ 69,608 year)
- Kingston, ON (from $ 63,103 to $ 64,241 year)
- North York, ON (from $ 54,764 to $ 58,500 year)
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Clinic Study Assistant
Pharma Medica Research Inc.Scarborough, ON, Canada- Full-time
Job Description
Job Description
Pharma Medica Research Inc. is a full-service contract research organization in need of a Clinic Study Assistant to join our team in Scarborough! The Clinic Study Assistant assists with general clinical duties as required by Pharma Medica Research Inc. ( PMRI ). This position reports to the Manager, Group Leader / or designate.
Duties and Responsibilities
Responsibilities include but are not limited to :
- File and organize clinic files as per SOP.
- Monitor subject safety and compliance with study restrictions and study procedures.
- Direct subjects to designated stations for study procedures.
- Prepare the clinic to conduct clinical studies (i.e., tube labelling, bunk room preparation, set up bleeding stations, stock supplies, medical equipment etc.).
- Perform clinical procedures such as but not limited to : study check-in procedures, belongings search, mouth check, meal monitor, etc., according to the study protocol and / or SOP requirements.
- Process biological samples as required to conduct a clinical study.
- Perform general cleaning duties (i.e. decontaminate workstations, pack and remove biohazard bins to designated waste rooms, and equipment cleaning such as blood pressure machines, centrifuges and fridges).
- Properly complete documentation of clinical activities according to GCP, SOP guidelines, and / or regulatory requirements.
- Perform any tasks required by the Group Leader, MLA / Study Coordinator deemed necessary to conduct a clinical study.
- Other duties as required.
Qualifications :
Minimum level of academic or formalized training.
We Offer
Please note all applications must be eligible to work within Canada.
PMR I is an Equal Opportunity Employer; promoting accessibility and inclusivity at work and offering accommodation for applicants as required and requested.
We thank all applicants for their interest; however, only those selected to proceed in the interview process will be contacted.
If you meet the qualifications and are looking for an exciting place to work, apply today!