Drive impactful clinical data management projects in a remote contract role. Collaborate with industry professionals to ensure regulatory compliance and data accuracy. Enhance your expertise in a dynamic, fast-paced environment.
Associate Director, Clinical Data Management
in Healthcare + Life Sciences ContractJob Detail
Job Description
Overview
- Lead clinical data management activities for multiple studies, ensuring accurate and complete data for analysis and regulatory submission.
- Oversee vendor partnerships and ensure compliance with performance metrics and timelines.
- Develop and maintain clinical trial databases adhering to industry standards and regulatory requirements.
- Coordinate data review and validation processes to ensure data consistency and accuracy.
- Support regulatory submissions by ensuring complete and accurate clinical trial documentation.
- Provide leadership and training to the data management team, fostering professional growth.
- Contribute to departmental SOP development and quality assurance processes.
- Collaborate with cross-functional teams to ensure high-quality data output and adherence to project timelines.
Key Responsibilities & Duties
- Act as the data management lead for clinical studies, overseeing database setup through closeout.
- Manage vendor partnerships and ensure adherence to performance metrics and deliverables.
- Review protocols and study documents to ensure accurate data capture and compliance.
- Coordinate data review processes and ensure audit-ready project documentation.
- Develop and track internal performance metrics for data management activities.
- Support clinical documentation preparation for regulatory submissions.
- Assist in departmental resource planning and performance evaluations.
- Ensure compliance with GCP, SOPs, and regulatory requirements in all data management activities.
Job Requirements
- Bachelor’s Degree in Science or related field required.
- Minimum 10 years of clinical data management experience in biotechnology or pharmaceutical industry.
- Advanced knowledge of data management processes, systems, and regulatory requirements.
- Proficiency in setting up clinical databases in Medidata Rave.
- Strong organizational skills to manage projects, timelines, and budgets effectively.
- Excellent written and verbal communication skills.
- Ability to travel domestically and internationally up to 20%.
- Self-motivated, adaptable, and resourceful in a fast-paced environment.
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