Study Management: Oversees daily clinical trial operations, ensuring protocols are followed.

Patient Care: Coordinates patient recruitment, consent, and follow-ups.

Data Collection: Accurately captures and records study data for analysis.

Regulatory Compliance: Ensures trials adhere to FDA, ICH, and GCP standards.

Data Collection: Gathers accurate clinical data from study participants.

Patient Interaction: Assists in recruiting, screening, and monitoring study subjects.

Protocol Adherence: Ensures all clinical procedures align with study protocols.

Sample Handling: Prepares and stores biological samples for analysis.

Study Oversight: Manages end-to-end clinical trial projects, ensuring timelines are met.

Stakeholder Communication: Serves as a liaison between sponsors, investigators, and research teams.

Budget Management: Oversees the trial budget, controlling costs and allocating resources.

Risk Management: Identifies potential challenges and implements mitigation strategies.

Patient Care: Provides specialized care to clinical trial participants, ensuring their safety and well-being.

Study Protocols: Administers treatments and collects data as per research protocols.

Adverse Events: Monitors and reports any unexpected reactions or complications.

Patient Education: Informs participants about study details, procedures, and potential risks.

Sample Collection: Draws blood, collects biopsies, and handles other clinical specimens.