ob Description
Ensures data management activities and deliverables for area(s) of responsibility are completed in line with business requirements and company objectives.
Supervises assigned programs/TAs or/and direct reports who are responsible to lead and manage DM tasks outsourced to external vendors and ensure that milestones, deliverables, quality and timelines are met within budget and in accordance with regulatory requirements. Associate Director can have direct study responsibility.
The Associate Director level is expected to represent DM as key stakeholder on important company initiatives, audits/inspctions and support the development and implementation of the DM strategic vision and roadmap.
Qualifications
At least nine years of data management or relevant experience.
Bachelor's Degree or higher, or equivalent amount of combined educational and work experience is required. Exceptional candidates may be considered with less years depending on experience and education.
Significant experience in managing outsourced data management activities.
Significant experience with computerized clinical data management systems.
Proven success working in a virtual, global and multi-cultural environment.
Proven success in identifying creative solutions to complex study-related or technical issues.
Thorough understanding of the drug development process, clinical trial methodology, GCP regulations, and data management principles is required.
Strong understanding and experience with eCOA and ePRO systems and leading stuides with eCOA.
Strong and effective oral and written communication, project management, and interpersonal skills are required.
Professional accuracy, integrity, dedication and motivation and ability to influence and negotiate.
CCDM is preferred.
Knowledge of SAS and database programming, systems integration experience and understanding of CDASH and CDISC standards are preferred.
https://careers.teva/job/Netanya-1111/724323800/