Emmanuel Woods

Support nurse case managers by coordinating healthcare documentation, communication, and care management activities.

Maintain accurate electronic files, medical records, and confidential healthcare documentation while ensuring HIPAA compliance.

Coordinate communication between providers, clients, vendors, and internal teams to support timely care coordination.

Review medical documentation and assist with healthcare data collection, reporting, and quality initiatives.

Prepare correspondence and reports while maintaining accuracy, organization, and attention to detail.

Utilize healthcare systems and Microsoft Office tools to manage workflows and multiple priorities.

Coordinated clinical research activities including participant scheduling, study visits, data collection, and protocol-related tasks.

Supported informed consent processes, participant communication, and research visit coordination within a specialty care environment.

Maintained source documentation, study records, and research files while supporting compliance with research standards.
Utilized Epic EMR for chart review, clinical documentation, and accurate research data collection.

Collaborated with physicians, healthcare providers, and research teams to support study execution.
Performed data entry, quality checks, and documentation review to maintain research data accuracy.

• Performed venipuncture and specimen collection while ensuring patient safety and specimen integrity.
• Managed specimen identification, labeling, processing, and documentation according to laboratory standards.
• Supported daily operations by coordinating workflow and assisting team members.
• Trained staff on collection procedures, safety practices, and organizational standards.
• Collaborated with nurses, providers, and laboratory personnel to support patient care.
• Maintained HIPAA compliance and infection control standards in a clinical environment

Supported clinical research laboratory operations through specimen processing, documentation, and protocol-specific procedures.

Followed SOPs, GCP principles, and quality standards while supporting clinical trial activities.

Maintained specimen integrity through accurate labeling, tracking, processing, and shipment procedures.

Assisted with laboratory documentation, quality control processes, and research sample management.

Collaborated with research coordinators and laboratory teams to support study timelines.

Maintained a safe, organized, and compliant laboratory environment.