• Evaluating and tracking the eligibility of all patients seen in the clinic. • Recruits subjects to participate in the assigned study by using approved methodologies, such as, reaching to healthcare providers for referrals, visiting clinics, using approved advertisements. • Conducts the enrollment of study participants, including explaining research procedures, and obtaining informed consent of subject and registering patients to cohort studies and other protocols. • Schedules appointments of study participants; conducts reminder phone calls and/or sends mail-outs. • Performs biospecimen collection for study purposes, including but not limited to: blood (phlebotomy), saliva (cheek swabs), urine collection, breastmilk collection, and placental tissue. • Performs office-related duties such as answering phones, picking up and delivering mail, storing and distributing office supplies, handling faxes, scanning, filing, photocopying, collating materials, maintaining the update of policy manuals, etc. • Participates in staff meetings/initiatives including appropriate quality improvement and education activities, or if unable to attend non-mandatory activities, accepts responsibility to review meeting minutes and becomes knowledgeable of issues discussed. • Reviews and abstracts the medical records for patients, including review of all records for inclusion/exclusion criteria. • Accessing patient demographic and clinical information from the clinical systems. • Entering information into the appropriate EMR and eCRF systems and departmental systems in an accurate manner. • Supervises and trains student research assistants in EMR data abstraction and data entry. • Reviewing data for quality and completeness for each enrollee for completion and quality (QA). • Answers queries; performs data collection entry into database; maintains clear, concise, accurate and legible records. • Assists with the coordination of the collection, processing, organization, and storage of biological specimens in the systems • May assist in the preparation for IRB and regulatory submissions and maintenance of regulatory files • Maintaining on-going communications with research managers and PIs for data collection needs.