Clinical Research Associate I Professional

2 weeks ago


Townsville, Queensland, Australia Syneos Health, Inc. Full time
Job Overview

Syneos Health, Inc. is seeking a highly skilled Clinical Research Associate I Professional to join our team. As a key member of our clinical operations department, you will be responsible for ensuring the integrity and quality of clinical trials conducted at investigator sites.

Your primary responsibilities will include site qualification, site initiation, interim monitoring, site management, and close-out visits. You will ensure regulatory compliance and adherence to Good Clinical Practice (GCP) guidelines. Additionally, you will verify the process of obtaining informed consent, assess factors that might affect subject safety and clinical data integrity, and conduct source document reviews.

You will also utilize available hardware and software to support the effective conduct of clinical study data review and capture. Your expertise in GCP/local regulations and organizational procedures will ensure that investigational products are appropriately managed and stored. You will document activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents.

A successful candidate will have excellent communication, presentation, and interpersonal skills, with the ability to manage required travel of up to 75%. You will work collaboratively with project site personnel, including acting as a primary liaison, ensuring all assigned sites and project-specific site team members are trained and compliant with applicable requirements.

We offer a dynamic and inclusive work environment where you can grow and advance your career. Our company culture values diversity, equity, and inclusion, and we strive to provide opportunities for professional development and recognition.



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