The Phlebotomist (or Certified Medical Assistant) will be responsible for assisting the clinical research staff in conducting clinical research trials.
DUTIES & RESPONSIBILITIES
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Assisting in the collection and recording of patient data per Sponsor requirements via the respective EDC system.
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Timely and accurately assist in collection, management, and shipment of subjects' samples, and/or specimens
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This includes completing the above-mentioned training prior to any study-related procedures being conducted on that said protocol should the RA be added to a protocol post-study start.
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Maintaining clear, concise, accurate, and legible records.
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Being prepared for and available at all required company meetings and monitoring visits for their assigned protocols at their respective site(s).
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Utilizing the most recent version of the Protocol, Informed Consent, and Investigator Brochures at their respective site(s).
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Conducting patient visits.
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Assisting in reporting Adverse and Serious Adverse Events to the appropriate authorities per Sponsor.
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Assisting in addressing and resolving issues from internal/external audits and monitoring letters for all assigned protocols at their respective site(s) in a timely manner.
KNOWLEDGE & EXPERIENCE
Education:
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High school diploma or equivalent required
Experience:
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Prior experience in clinical research is not required but preferred
Credentials:
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Phlebotomist certificate preferred
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Medical Assistant Certification preferred
Knowledge & Skills:
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Knowledge of medical terminology required
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Must be detail-oriented and demonstrate attention to detail
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Excellent customer service skills
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Excellent computer skills
