On Site EMT - Biolife Plasma Services

Job Title: Clinical Research Associate

Responsibilities:

• Conduct site monitoring visits to ensure compliance with study protocols.
• Collaborate with cross-functional teams to support clinical trial activities.
• Review and verify data for accuracy and completeness.
• Assist in the preparation of study documentation and reports.
• Provide training and support to site staff on study procedures.

Qualifications:

• Bachelor’s degree in Life Sciences or related field.
• 2+ years of experience in clinical research.
• Strong knowledge of GCP and regulatory requirements.
• Excellent communication and organizational skills.
• Ability to travel as needed for site visits.