Phlebotomist (Night Shift)

Pharma Medica Research Inc.•Scarborough, ON

1d•CA$18 - CA$18•Onsite

About The Position

Pharma Medica Research (PMRI) Inc. is a Contract Research Organization that strives for innovation and original solutions in a highly regulated and competitive industry. If your career goals align with innovation and original thinking you will be the perfect candidate to be part of an inclusive, adaptable, and forward-thinking organization. Our reputation for delivering high quality research is outstanding. At PMRI we are committed to making a difference in healthcare and people’s lives. Come join our team! We have an exciting opportunity for a part-time Phlebotomist (Night Shift) within our PMRI clinic located in Scarborough, Ontario. In this role, you will perform clinical procedures at Pharma Medica Research Inc. (PMRI). This position reports to the Group Leader, MLA.

Requirements

Post-secondary degree or equivalent.
Completion of recognized Phlebotomy/ECG program.
Availability to work night shift 10:00 pm to 6:00 am.
6 months to 1 year of recent venipuncture experience.
1 year of CRO experience or equivalent.
Good verbal and written English communication skills.
Good interpersonal skills.
Good organizational skills.
Good computer skills.
Ability to work both independently and as a team member.
Detail oriented and able to manage workload in a fast-paced environment.
Excellent in hands-on learning.
Ability to work multiple tasks simultaneously.

Nice To Haves

OSMT certification is an asset.
Current CPR certification is an asset.
Benchtop laboratory work experience is an asset.

Responsibilities

Perform clinical procedures such as but not limited to: study check in procedures, subject and belongings search, mouth check, blood sample collection, sample processing and storage, meal monitor, etc., according to the study protocol and/or SOP requirements.
Collect and process biological samples as required to conduct a clinical study.
Monitor subject safety and compliance with study restrictions and study procedures.
Perform general clinical duties to prepare for the clinical study (i.e. tube labelling, bunk room preparation, 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 regulatory requirements.
Perform any tasks (e.g. administrative work, tube labelling, sample bundling etc.) required by the Group Leader, MLA/Study Coordinator deemed necessary to conduct a clinical study.
Perform safety monitoring and adverse event documentation only if the training is complete.
Handle medical emergency situations with the study supervisor during the night.