Job Description

Key Responsibilities:

Laboratory Duties:

• Perform venipuncture, process, pack, and ship samples following IATA regulations.
• Review and file laboratory results, ensuring proper documentation.
• Monitor and order study lab kits and supplies as needed.
• Supply chain responsibility for lab.

Patient Recruitment and Screening:

• Proactively recruit study patients and conduct phone screenings according to protocols.
• Ensure patient consent forms are read, understood, and properly signed; provide patients with copies of consent forms.

Data Management:

• Collect clinical data including chart documentation, patient histories, medications, vital signs,
• ECGs, and protocol-required procedures.
• Utilize Electronic Data Capture systems and ensure accurate data entry in CTMS (clinical trail management system)

Study Support:

• Assist Clinical Research Coordinators in daily tasks, including organizing necessary documents and materials.
• Assist with daily administrative duties.

Regulatory Compliance:

• Comply with all HIPAA, CLIA, OSHA, FDA, and ICH regulations, as well as confidentiality agreements.

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