POSITION OPEN ONLY FOR THE PHILIPPINES 100% REMOTE POSITION Position : Clinical Research Associate Working Hours: US Working hours Salary Range: $1.500 - $1.700 Usd Based on experience About the Company The company specializes in providing cloud-based telemedicine solutions.

Offering a comprehensive platform designed to streamline and enhance the delivery of virtual healthcare services.

The services typically include features such as secure video consultations, appointment scheduling, patient management, and electronic health record integration.

The company aims to improve access to healthcare by enabling medical professionals to connect with patients remotely thus supporting efficient and effective healthcare delivery.

Duties and responsibilities: Trial Coordination : Coordinate/Schedule meetings related to clinical trial activities and draft meetings agendas, materials, and minutes as required.

Data Management Support : Assist in data management activities, including data cleaning and query resolution to ensure accurate and timely collection of clinical trial data.

Assist in updating study databases and maintaining accurate records of trial- related activities.

Site Management : Support investigative site activities by monitoring and managing correspondence in the study mailboxes to address or escalate site-related issues throughout the trial lifecycle Quality Assurance : Participate in quality assurance activities, including internal audits and inspections to ensure compliance with regulatory requirements and adherence to quality standards.

Documentation Management : Assist with maintaining accurate and up-to-date trial documentation, including trial master files, study files and regulatory authorities Regulatory compliance : Ensure study compliance with good clinical practice guidelines, standard operating procedures, and regulatory requirements throughout the conduct of clinical trials.

Requirements: Bachelor's degree in a relevant/similar scientific discipline At least 2 years of experience in clinical research field Clinical Research Associate Training or similar is a plus Experience using electronic data capture (EDC) systems, TMF or ISF maintenance experience is a plus.