Associate Director, Data Management

Company Info

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job 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.

Function

Sub Function

Reports To

Director, Data Management, Data Management SCD (ISR)

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Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.