POSITION SUMMARY:

The Clinical Research Coordinator (CRC) will play a key role in supporting research activities within the Translational Research Laboratory and Bio-specimen Repository in the Section of Hematology & Medical Oncology. Responsibilities include obtaining informed consent for research studies and biobank enrollment, abstracting data from medical records, maintaining patient databases, and processing and managing bio-specimen samples.
The CRC will ensure all activities are conducted in accordance with institutional policies, IRB regulatory requirements, and ethical research standards. The role also involves assisting with literature reviews, preparing study data and reports, and contributing to manuscript development.

EDUCATION/EXPERIENCE:

• Bachelor’s degree required AND
• 0-2 years of experience
• Experience in clinical research, patient recruitment, or biospecimen handling preferred.

KNOWLEDGE AND SKILLS:

• Ability to work independently while effectively managing time and multiple priorities.
• Excellent communication, organizational, and problem-solving skills.
• Ability to work effectively with diverse patient populations.
• Proficiency in Microsoft Office; experience with research databases or electronic medical record (EMR) systems a plus.

JOB RESPONSIBILITIES:

• Recruit, screen, and obtain informed consent from patients for research studies and biobank participation.
• Process, label, store, and ship biospecimen samples according to study protocols and quality standards.
• Maintain accurate research records, databases, and regulatory documentation.
• Collaborate with clinical and research teams to coordinate study activities.
• Conduct literature searches and assist with data analysis, interpretation, and reporting.
• Ensure patient privacy and compliance with all regulatory and confidentiality guidelines.