- Foster strong site relationships from start to finish of the trial
- Conduct monitoring activities in compliance with regulations and protocols
- Understand study protocols thoroughly
- Coordinate tasks with other sponsor roles
- Oversee site visits remotely and on-site to ensure data accuracy and subject safety
- Manage regulatory documentation and communicate with Investigators
- Resolve site performance issues and escalate when necessary
- Expect to travel approximately 65%-75% of the time
- Current driver's license preferred
- Bachelor's degree in science or biology
- Minimum 2 years of clinical research experience
- Fluent in Local Languages and English, with strong communication skills
- Good understanding of clinical research and regulations
- Hands-on knowledge of Good Documentation Practices
- Ability to manage complex issues and perform root cause analysis
- Effective time management and conflict resolution skills
- Capable of working independently and in multicultural environments
- Demonstrates commitment to customer focus
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Associate Clinical Research Associate - Washington, United States - Merck
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Description
Exciting Opportunity as an Associate Clinical Research Associate - Northeast Region (Remote)
Join our team as a crucial primary site contact and manager for a clinical research study. Develop strong relationships with sites throughout the trial, ensuring compliance with protocols and regulations.
Extent of Travel:
About the Company:
The company is dedicated to fostering diversity and inclusion in the workplace, welcoming individuals from all backgrounds. Embrace innovative ideas and work collaboratively in an inclusive environment.