Principal Clinical data manager Jobs – Novartis – Hyderabad

Novartis looking for individuals with end to end experience in clinical data management. You will play a key role in providing leadership to various teams and developing cross-functional data cleaning strategies.

Novartis Hiring Notification for Principal Clinical Data manager Position at Hyderabad Location

key responsibilities:
Your responsibilities include, but are not limited to:

• Provides Data Management leadership for one or more assigned programs or indications.
• Demonstrates a business understanding of the compound profile to identify and assist in successful application of consistent data management processes and documentation across assigned programs, i:e ensuring consistency across data quality plans
• Develops an understanding of CDISC or other recognized industry standards and how these impact the programming team. Ensures consistency of program level standards
• Communicates and negotiates effectively with all other Program level team members. Primary point of contact for DM at the GPT level
• Maintains awareness of the status of start up, conduct and finalization activities for all trials within assigned program(s) Tracks and requests necessary resources. Demonstrates an effective application of knowledge across all DM scenarios. Is able to provide solutions to effectively meet timelines
• Manages effective escalation of issues in order to keep stakeholders appraised of DM activities and proposed resolutions
• Supervises and drives the overall DM timelines across assigned programs. Reviews the Data Management Metrics on the assigned Program. Coaches and mentors associates as required, ensures that DM associates on the program are aware of the risks, priorities, goals and impact of the work contribution.
• Develops risk management strategies to prevent data quality issues from derailing projects
• Represents Data Management at cross functional forums, meetings and provides timely feedback to partners. Understands Health Authority requirements and is able to prepare for and participate in Health Authority inspections and audits as required

Minimum requirements

• Experience : University or college degree in life science, computer science, pharmacy, nursing or equivalent relevant degree with Ideally 8 years’ experience in Drug Development with at least 5+ years’ in Clinical Data Management
• Strong leadership, collaboration and organizational skills with proven ability to successfully manage simultaneous trials and meet deadlines
• Excellent understanding of clinical trials methodology, GCP and medical terminology
• Must be able to anticipate challenges and risks and proactively suggest/implement solutions
• Ability to work under pressure demonstrating agility through effective and innovative team leadership
• Excellent interpersonal skills and proven ability to operate effectively in a global environment. Ability to influence and communicate across functions and to external stakeholders
• Understanding of project management concepts in order to aid delivery across a program