Contract Virtual Clinical Coordinator

This is a fully remote position, open to applicants in District of Columbia, +1 more state.

📋 Description

• Perform remote clinical activities following study protocols, SOPs, and GCP guidelines.

• Identify, recruit, and enroll qualified patients for clinical trials through virtual means.

• Gather, maintain, and securely manage clinical research data.

• Inform potential participants and oversee informed consent via virtual interactions.

• Assist participants and send reminders to enhance study adherence.

• Carry out follow-up activities related to clinical trials.

• Monitor participants, promptly report adverse events, and ensure adherence to IRB-approved protocols.

• Provide support for the research participant call center.

• Uphold professionalism in all participant interactions.

• Aid in managing study equipment, including tracking, functionality, and documentation.

• Relay updates and offer assistance to MCRA clinical affairs staff and clients under the guidance of senior staff.

• Undertake additional tasks and projects as assigned.

⛳️ Requirements

• A Bachelor’s degree is required, preferably in a life sciences or healthcare-related discipline.

• At least three years of experience as a Clinical Coordinator or in a similar clinical research position.

• Exceptional attention to detail.

• Outstanding verbal and written communication abilities.

• Familiarity with study-specific software applications and equipment.

• Understanding of Standard Operating Procedures (SOPs), Manual of Procedures, and Good Clinical Practice (GCP).

• Availability to work weekday hours from 1:00 PM to 9:00 PM PST.

• Capability to work on Saturday and/or Sunday from 10:00 AM to 6:00 PM PST.

🏝️ Benefits

• Opportunities for incentive plans, bonuses, and/or other forms of compensation.

• Health, welfare, and/or additional benefits.