Core Responsibilities

Act as the primary point of contact for the sponsor at the investigative site. Conduct site assessments, training, routine monitoring, and site closure activities in compliance with protocols and regulations. Collect local insights and utilize engagement tools to report and track progress. Ensure data quality and timely submission from study sites, and manage investigator payments as per contractual obligations.

Requirements

Bachelor's degree in health-related fields (e.g., Medicine, Biological Sciences, Pharmacy, Nursing) preferred. Minimum of 3 years of clinical experience, with 2 years in independent monitoring of clinical research studies. Familiarity with risk-based monitoring approaches and knowledge of applicable therapeutic area indications.

Additional Information

Experience Level

Senior

Employment Type

permanent

Work Mode

Remote