Clinical Research Coordinator

Key Responsibilities

• Perform venipuncture and other approved specimen collections in accordance with study protocols and regulatory requirements.
• Ensure proper specimen labeling, handling, processing, storage, and transport.
• Follow all infection control, safety, and biohazard procedures at all times.
• Support clinical research studies through accurate documentation and strict protocol compliance.
• Aid in study logistics, including coordination of collection events and research workflows.
• Report deviations, issues, or adverse events promptly and accurately.
• Provide a calm, professional, and respectful experience for all study participants.
• Clearly explain procedures and address participant questions with confidence and empathy.
• Maintain strict confidentiality and uphold HIPAA and data privacy standards.
• Adhere to Alden Scientific SOPs and research protocols with a high level of precision.
• Maintain accurate records, chain-of-custody documentation, and study logs.
• Represent Alden Scientific professionally while traveling to and working at external sites.

Required Qualifications

• Phlebotomy experience or willingness to be trained in phlebotomy.
• Strong understanding of clinical research or laboratory best practices.
• Ability to follow detailed protocols and maintain meticulous documentation.
• Willingness and ability to travel as required.

Preferred Qualifications

• Prior experience in clinical research, clinical trials, or research sample collection.
• Experience with mobile or travel-based phlebotomy.
• Excellent communication and interpersonal skills.
• Comfortable working flexible or occasional non-standard hours as needed.