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Responsibilities:
- Collaborate with stakeholders to define data elements and develop CRFs.
- Liaise with database vendors and perform UAT for database builds.
- Draft and maintain Data Management Plans and ensure data quality.
Requirements:
- Bachelor's degree in a scientific discipline with 5+ years in medical device studies.
- Knowledge of GCP, ICH, GDPR, and FDA/EU regulations.
- Strong expertise in clinical database development and validation.
Benefits:
- Annual salary range of $105,000-$130,000.
- Comprehensive benefits including medical, dental, vision, and 401(k).
- Remote work with occasional travel and paid time off.
Partner Company
They develop innovative medical technology and manage clinical data for medical device studies. They operate in a fast-paced, collaborative environment with a focus on quality and regulatory compliance.