Manager Clinical Data Management

About the Opportunity:
You will have the opportunity to work with cutting-edge RNA-based therapeutics research, collaborating on groundbreaking treatments for challenging diseases. Contribute to addressing genetic-based diseases and potentially make a significant impact on patients' lives by targeting disease-related proteins. Explore diverse therapeutic areas beyond liver diseases, fostering professional growth and development in a dynamic environment. Experience a collaborative work environment where science-driven innovators prioritize teamwork, providing opportunities for idea exchange and collective efforts to bring new therapies to patients. Work with our client at strategic locations across the U.S., facilitating collaboration with experts from various fields.

Responsibilities:
Lead data management for clinical trials from launch to closeout.
Coordinate with vendors and senior management.
Ensure compliance with regulations and quality standards.
Manage data collection, review, and reporting.
Develop and implement departmental policies and process improvements.
Requirements:
Bachelor's degree.
5+ years in pharmaceutical/biotech roles managing multiple trials.
Strong communication and interpersonal skills.
Knowledge of GCP, CDISC, FDA, and ICH guidelines.
Experience with EDC vendors and processes.

Preferred:
Master's degree.
Supervisory experience.
Proficiency in Medidata Rave or similar tools.
Familiarity with Spotfire or other programming tools.
Additional Information:
This is an onsite role.

A relocation package can be offered.
Pay Range (California): $110,000—$150,000 USD

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