As a Clinical Operations Specialist, you will be responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures, and Work Instructions.

Key responsibilities include:

• Assisting Clinical Monitoring staff with site management activities, including serving as a Sponsor representative for sites on assigned studies
• Creating and maintaining Trial Master File (TMF) and project files
• Preparing and maintaining site manuals, reference tools, and other documents
• Maintaining and updating clinical tracking information in databases
• Tracking incoming and outgoing clinical and regulatory documents
• Coordinating the ordering, packaging, shipping, and tracking of site supplies and materials
• Assisting with coordination of team meetings and preparing meeting minutes

Requirements:

• High School diploma or equivalent
• Good communication and interpersonal skills
• Ability to embrace new technologies
• Minimal travel up to 25% may be required

Syneos Health offers a range of benefits, including career development and progression, supportive line management, technical and therapeutic area training, and total rewards programs.

The company is committed to its Total Self culture, which encourages employees to be themselves and provides a supportive and inclusive work environment.

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