Data Management Leader at United Brands Group
2 weeks ago
We are seeking a highly skilled Senior Principal Clinical Data Scientist to join our team at United Brands Group. This is an exciting opportunity for a motivated and experienced professional to lead our data management efforts in clinical trials.
About the RoleThe Senior Principal Clinical Data Scientist will be responsible for managing all data management deliverables at a consistently high standard, ensuring that data quality meets regulatory requirements and timelines are met. The successful candidate will provide leadership and coaching to junior team members, ensuring consistency across assigned programs.
Key Responsibilities- Data Management Leadership: Provide DM leadership across assigned trials and programs, ensuring strong DM representation across the CTT.
- Business Acumen: 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.
- Strategy Alignment: Ensure alignment with the TA level data strategy as defined by the TA Data Strategy Director, proficient in relevant CDISC or other recognized industry standards, and how these impact the programming team.
- Risk Management: Maintain awareness of the status of start-up, conduct, and finalization activities for all trials within assigned programs, track and request necessary resources, ensure key study risks & issues are shared in the Project Review Meeting led by Sr GHs/GHs.
- Timely Delivery: Supervise and drive the overall DM timelines across assigned programs, reviews the Data Management Metrics on the assigned Program.
- Development and Training: Coach and mentor associates as required, ensures that DM associates on the program are aware of the risks, priorities, goals, and impact of the work contribution.
- Subject Matter Expertise: Act as subject matter expert (SME) or, as assigned, lead process improvement/non-clinical project initiatives, ensure adherence to ICH GCP, DM standards, SOPs/WPS, and process guidelines.
To be considered for this role, you should have:
- A degree in life science, computer science, pharmacy, nursing, or equivalent relevant degree.
- At least 8 years' experience in Drug Development, with 5+ years in Clinical Data Management.
- Excellent verbal and written skills, strong leadership, collaboration, and organizational skills, 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.
- Ability to work under pressure, demonstrating agility through effective and innovative team leadership.
We offer a competitive salary range of $120,000 - $180,000 per annum, depending on experience, plus a comprehensive benefits package and opportunities for career growth and development.
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