Source Document Writer

• Palm Research Center Full-Time | Monday-Friday, 7:30am-4pm About the Role Join our clinical research team as a Source Document Writer, responsible for creating and maintaining accurate, complete, and timely source documentation within our real-time Clinical Trial Management System (CTMS).

You'll play a key role in supporting clinical trial operations, working closely with Principal Investigators, Clinical Research Coordinators, and Regulatory staff to ensure study records meet GCP and protocol requirements. What You'll Do

• Document clinical visits, procedures, assessments, medications, adverse events, and lab results per protocol
• Enter and maintain accurate records in real time within the CTMS
• Review documentation for completeness and resolve discrepancies with the research team
• Support audit and inspection readiness (sponsor, monitor, and regulatory)
• Follow

ICH-GCP, FDA

regulations, and company SOPs

• Collaborate with investigators and coordinators to ensure documentation accuracy What We're Looking For
• 1-3+ years of experience in clinical research, clinical/medical documentation, or a related healthcare field
• Strong medical terminology knowledge and written communication skills
• Exceptional attention to detail and accuracy
• Ability to manage multiple studies and deadlines
• Comfort learning new software systems Preferred
• Bachelor's degree in clinical research, healthcare, nursing, or life sciences
• CRC experience; familiarity with eSource, EDC, CTMS, or EMR/EHR platforms
• Knowledge of

FDA/ICH-GCP

guidelines

Pay:

$21.00

• $24.

00 per hour Expected hours: 40.0 per week

Benefits:

401(k) Health insurance Health savings account Life insurance Paid time off Vision insurance

Work Location:

In person