Work Location: Anne Arundel County, Maryland

Summary:

The Clinical Research Coordinator oversees the daily operations of clinical trials, focusing on oncology studies. This full-time, on-site position is responsible for ensuring protocol compliance, subject safety, and accurate documentation throughout the research process.

Responsibilities:

• Coordinate all aspects of clinical trial operations, including screening, enrolling, and following study participants.
• Ensure strict adherence to study protocols, informed consent processes, and regulatory requirements.
• Develop and implement effective subject recruitment strategies to meet enrollment goals.
• Prepare and maintain study charts, binders, supplies, and calibrate research equipment as needed.
• Verify participant eligibility and perform delegated protocol-specific tasks, including phlebotomy/blood draws.
• Document all study procedures, adverse events, and medication changes accurately and in a timely manner.
• Communicate with investigators and clinical staff regarding study drug administration and imaging procedures.
• Assist with monitoring visits, promptly report serious adverse events and protocol deviations, and resolve action items.

Qualifications:

• Minimum High School Diploma or GED required.
• At least 5 years of US-based clinical research coordinator experience (foreign experience not accepted).
• Oncology clinical research experience is required.
• Phlebotomy/blood draw skills strongly preferred.
• Certification from ACRP or SOCRA preferred.

Published Category: Clinical Operations & Development