Prin Clin Data Scientist (Data Mgr)

Novartis • East Hanover, NJ

306d • $114,000 - $211,000 • Onsite

About The Position

Love clinical data management? Bring that passion to Novartis! This key Principal Clinical Data Scientist will be responsible and accountable for managing all Data Management deliverables at a consistently high standard with respect to cost, quality, and timelines for all assigned indications within one or more Global Clinical Program(s)/Project(s).

Requirements

• Bachelor's degree in life science, computer science, pharmacy, nursing or closely related discipline.
• 5 years' experience in Drug Development with at least 3+ years' in Clinical Data Management.
• Demonstrated 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.
• Proven ability to interrogate and view data through various programming/GUI techniques.
• 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.

Nice To Haves

• Experience supporting Neuroscience or CRM.

Responsibilities

• Provide DM leadership across assigned trial(s) and Program(s) ensuring strong DM representation across the CTT.
• Acts as an ambassador for CDAM across the organization, showcasing business value and benefits.
• Demonstrate a business understanding of the compound profile and data strategy to identify and assist in successful application of consistent data management processes and documentation across assigned programs.
• Ensure alignment with the TA level data strategy as defined by the TA Data Strategy Director.
• Competent in relevant CDISC or other recognized industry standards and how these impact the programming team.
• Maintain awareness of the status of start-up, conduct and finalization activities for all trials within assigned program(s).
• Tracks and requests necessary resources.
• Ensures the key study risks & issues are shared in the Project Review Meeting led by Sr GHs/GHs.
• Provide accelerated feedback to assure well written, stable protocols and amendments.
• Recognize and resolve protocol issues that may impact database.

Benefits

• 401(k) eligibility
• various paid time off benefits, such as vacation, sick time, and parental leave

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Industry: Chemical Manufacturing
• Education Level: Bachelor's degree