Principal Clinical Data Manager

What we look for

• Bachelor’s degree in a related field & 7+ years of relevant experience; at least 5 years’ experience in clinical data management experience in a clinical research setting and 4 years of experience in leading project teams, required.
• Thorough knowledge of International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines as well as of medical terminology, clinical trials, and clinical research.
• Working knowledge of the relationship and regulatory obligation of the contract research organization (CRO) industry with pharmaceutical / biotech companies.
• Demonstrated ability to lead by example, and demonstrated skill for technical leadership of staff.
• Demonstrated ability to serve as a strong internal and external consultant, influence without authority, and guide project teams to mutually acceptable outcomes .
• Demonstrated ability to operate with the “big picture” in mind and serve as a thought partner to management as needed.
• Expert level skills in use of computer technology, including clinical trial databases and applications (e.g., IBM Clinical Development, Medidata RaveX), with a strong desire and ability to learn new applications.
• Detailed understanding of project planning and management methods.
• Excellent interpersonal, communication, and organizational skills with the ability to work independently and in a team environment.
• Ability to work in different projects with different priorities and act as team mentor, and provide data management expertise.
• Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.
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• Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.