Phlebotomists Group Leader

at  Pharma Medica Research Inc

Pharma Medica Research is a full service contract research organization specialized in conducting early phase clinical trials in healthy volunteers, special and patient populations. We are always looking for top talent to join our growing team! We’re currently looking for a Group Leader to join our phlebotomists team!
The Group Leader, MLA supervises and/or perform all aspects of the study procedures and ensure proper documentation of clinical activities are in compliance with Pharma Medica Research Inc (PMRI) SOP, GCP guidelines, FDA/TPP regulations. This position reports to Manager, Group Leaders and/or designate.

QUALIFICATIONS:

• B.Sc. degree or equivalent
• OSMT certification
• Minimum amount of practical work experience:
• 2-5 years CRO experience or equivalent.
• Previous MLA Group Leader designation.
• Excellent verbal and written English communication skills.
• Excellent interpersonal skills.
• Ability to work both independently and as a team member.
• Excellent organizational skills.
  If you’re interested in this exciting position, apply today

• Ensure management is kept up-to-date regarding all clinic activities.
• Assist in hiring new Medical Laboratory Assistants (MLAs).
• Responsible for training of new MLAs.
• Responsible to update training of MLAs on new and revised clinic procedures.
• Ensure training records for MLAs are updated.
• Responsible for delegation of clinic duties to all MLAs.
• Assist the study coordinators in updating all MLAs regarding the status of the study.
• Ensure general clinical duties are performed in preparation for clinical study (i.e. tube labeling, bunk room preparation, set up bleeding stations, etc).
• Prepare clinic assignment for each study.
• Supervise and/or perform all aspects of the study procedures and ensure proper documentation of clinical activities are in compliance with SOP, GCP guidelines, FDA/TPP regulations.
• Ensure general cleaning duties are performed (i.e. decontaminate workstations and equipment such as centrifuges).
• Ensure sufficient supplies are present in the clinic for upcoming studies.
• Assist in reviewing study documentation.
• Assist with responses to QA/QC findings and subject follow-up.
• Assist in performance evaluation of MLA’s. Participate regularly in all necessary PMRI training programs including SOP, GCP training, and PMRI in-house training modules.
• Ensure Joint Health and Safety rules and regulations are adhered to at all times.
• Other duties as required