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Phlebotomist

Location:	Mississauga, Ontario, Canada
Job Type:	Part-time
Posted:	9th Jul 2009
Closing Date:	17th Jul 2009
Posted By:	Allied Research International
Details:
Phlebotomist Cetero Research is a leading provider of early clinical, bioanalytical and specialty Phase II-IV research services to the bioanalytical, generic and pharma industries. We achieve this with personal attention to detail and consistently applying leadership, management, scientific and ethical rigor to everything we do. By creating a culture that fosters innovation, we continue to establish the benchmark for customer service, timeliness and quality in the CRO industry. We are presently recruiting for many new roles in both Canada and the USA. We are a team-based, client-focused group of professionals seeking to conduct the best quality research and we are looking for the best and the brightest to join our teams. POSITION SUMMARY: The incumbent in this role is responsible for the conduct of procedures required of study subjects for Phase I & Bioequivalence studies or Phase II-IV studies which include obtaining samples via venipuncture, processing of samples and other assigned tasks when required. GENERAL RESPONSIBILITIES: •Participate in the selection of subject’s for clinical trials and conduct procedure on study. Duties may include but are not limited to: •Procurement of blood samples •Obtaining ECGs •Obtaining vital signs •Performing a subject interview •Processing of blood and urine samples as per protocol requirements •Documenting and packaging of study samples for shipment to the appropriate clinical diagnostic laboratory or analytical laboratory •Obtaining subject’s Height, Weight, Elbow Breadth and Frame size •Performing urine and saliva screening for restricted substances •Study related tasks (such as Meals, Assembly, Check In procedures, Property Room, or as needed.) •Provide administrative support as required, including but not limited to copying, numbering, binding and archival of project and supporting documentation •Monitor subjects during in-house confinement periods for protocol and SOP requirement (posture, meals, activity restrictions etc.) •Work with the Quality Assurance group in the development/revision and implementation of Standard Operating Procedures as required •Ensure compliance with appropriate ARI SOP’s, GCP and ICH guidelines •Participate in training sessions •Work in a safe manner that does not endanger yourself or co-workers •Execute other duties as may be required by the Supervisor, Phase 1 & Bioequivalence Operations, study management staff, Director, Phase 1 and Bioequivalence Operations, Screening Coordinators or Phase II-IV staff, as training and experience allow. WORKING CONDITIONS AND ENVIRONMENT: •This role will require the flexibility to work a variety of shifts based on study design, including: day, evening and weekend •This role involves repetitive tasks such as: photocopying, archiving, transcription, binding, faxing •Requires working in a clinical office work setting and having direct contact with patients •Requires exposure to blood and body fluids while performing clinical procedures QUALIFICATIONS •2 year Medical Technology Diploma, or equivalent •2 - 4 years of recent phlebotomy and ECG experience •0 – 1 years of experience in a basic laboratory setting •Very organized, detail-oriented and able to multi-task •Requires tact and discretion in dealing with and handling confidential information •Strong patient interaction skills, proven experience in dealing with patients in a calm and friendly manner

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