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The Regulatory Coordinator prepares, organizes, and implements regulatory research documents, maintains regulatory compliance, and coordinates investigator training for clinical trials.

Coordinate all aspects of clinical trials ensuring adherence to ICH and GCP guidelines. Responsibilities include patient interaction, data management, and compliance monitoring.

As a Front Desk Receptionist, you will greet and assist patients and clients, answer calls, manage office tasks, and maintain a welcoming environment.

The Clinical Rater performs evaluations and assessments on study participants, confirming diagnoses and assessing various cognitive and functional statuses while ensuring data integrity and adherence to guidelines.

The Clinical Research RN is responsible for conducting nursing care, overseeing daily clinical study activities, and ensuring compliance with research protocols and documentation standards.

Ensure adherence to study protocols and quality assurance programs in clinical trials, supporting participant safety and data quality.

The Clinical Research RN I oversees daily clinical study activities, serving as a liaison between the site and Sponsor, ensuring accurate documentation and ethical conduct throughout the research process.

Prepare and manage regulatory documents for clinical research, ensuring compliance with FDA guidelines and training staff accordingly.

Coordinate all aspects of clinical trials, ensuring adherence to regulations and protocols, manage patient involvement, and assist with data analysis and reporting.

This role involves performing diagnostic testing and supporting laboratory activities, including sample collection, documentation, and ensuring compliance with protocols and regulations.