Clinical Research Coordinator

Overview

• The Clinical Research Coordinator oversees clinical trials, ensuring compliance with protocols and ethical standards.
• Collaborates with teams to manage research studies and participant interactions effectively.
• Responsible for data collection, analysis, and maintaining accurate research records.
• Supports logistics, ensuring equipment and supplies are available and functional.
• Works on-site full-time, traveling between designated locations.
• Provides oversight for 1-2 trials, monitoring participants’ health and adherence to protocols.
• Offers training opportunities for candidates with strong clinical research experience.
• Contributes to the success of oncology research studies.

Key Responsibilities & Duties

• Monitor and manage clinical trials, ensuring compliance with protocols and regulatory requirements.
• Collect and analyze research data, maintaining accurate and detailed records.
• Communicate with study participants, administering questionnaires and monitoring adherence to study rules.
• Collaborate with laboratories and regulatory bodies to ensure study compliance.
• Direct specimen collection, labeling, storage, and transport as per protocols.
• Ensure availability and functionality of necessary equipment and supplies.
• Recruit, interview, screen, enroll, and randomize study participants.
• Address protocol deviations and resolve queries related to electronic data capture systems.

Job Requirements

• Associate of Science degree in a health-related field; Bachelor's degree preferred.
• Minimum of 2 years of clinical research experience; oncology experience preferred.
• Proficiency in regulatory filing, study submission, and compliance monitoring.
• Strong skills in participant interaction, including informed consent and medical history collection.
• Experience in phlebotomy, vital signs monitoring, and ECG administration.
• Ability to manage stipend payments and administrative tasks effectively.
• Willingness to work on-site full-time and travel between designated locations.
• Strong organizational and communication skills to manage multiple trials simultaneously.