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Senior Clinical Data Scientist
Sandoz
posted 1mon ago
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Flexible timing
Key skills for the job
Job Description
Senior Clinical Data Scientist is responsible of using advanced data management tools and techniques, provide professional and lean execution of Data Management products and milestones with respect to cost, quality and timelines for all assigned trials within Clinical Data Acquisition and Management. Ensure consistently high-quality data available for analysis and reporting.
Key Responsibilities: -
- Provides DM leadership across assigned trial(s) Acts as the Trial Data Scientist where needed ensuring strong DM representation across the CTT.
- Demonstrates a business understanding of the compound(s) profile and data strategy to identify and assist in successful application of data management processes and documentation across assigned trials.
- Ensures 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.
- Provides accelerated feedback to assure well written, stable protocols and amendments. Recognize and resolve protocol issues.
- Performs DM activities for study start up including preparing the architecture and performing user acceptance testing (UAT).Manage local lab data flow and set up for the Clinical Database as applicable. Performs DM hands on activities during the course of the study, with a strong emphasis on quality, integrity and on-time delivery.
- Disseminates study level information to the Clinical Trial Team (CTT) and Program Clinical Data Scientist (PCDS). Supports and assists Junior staff for assigned trials
- Ensures Third party and other necessary reconciliation activities are performed for the study in a timely manner. Provides effective input into DM initiatives and innovations for quality, efficiency and continuous improvement in scientific and operational excellence
- Tracks and reports status and progress for assigned trials, indications or programs. Ensures adherence to ICH GCP, DM standards, SOPs/WPS and process guidelines.
Essential Requirements:-
- Timing and quality of database locks affecting submissions to regulatory authorities.
- University or college degree in life science, computer science, pharmacy, nursing or equivalent relevant degree.
- 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 stakeholder
- Proven ability to interrogate and view data though various programming/GUI techniques
- Excellent problem-solving skills, verbal and written skills
- Ideally 5 years experience in Drug Development with at least 4 years in Clinical Data Management.
Employment Type: Full Time, Permanent
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Flexible timing
Monday to Friday
No travel
Day Shift
Sandoz Benefits
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