Parita Sutariya Email and Phone Number

Phlebotomy & ECG Skills: Developing competence in blood collection and ECG procedures.Comprehensive Health Assessments: Conducting thorough basic and advanced evaluations.Mastering ICH GCP principles: Ensuring ethical and scientific standards in clinical trials.Coordinating Clinical Trials: Learning how to effectively plan and manage clinical trials.Monitoring Clinical Trials: Ensuring data integrity and adherence to regulatory standards.

• Ensures consent process is performed and documented in compliance with FDA, GCP, IRB, HIPAA, SOPs regulations and policies.• Extract data from source documents, complete case report forms, resolve sponsor queries.• Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.• Demonstrated ability to work independently with minimal supervision as well as cooperatively in a team environment.

• Implement quality control process throughout the conduct of the trial.• Coordinates the provision of support services to investigators and researchers.• Ensures the smooth and efficient day-to-day operation of research and data collection activities.• Monitors the progress of research activities; develops and maintains records of research activities, and prepares periodic reports, as required by investigators.

• Assists research personnel with multiple research projects• Pre-screens for eligible subjects for assigned studies based on written, broad eligibility criteria•Obtains consent from patients who will participate in non-interventional registry and observational studies, as well as some select, minimal risk device studies• Documents the informed consent process• Reviews eligibility criteria with the Principal Investigator and Clinical Research Coordinators/Nurses