Early Dev Global Study Data Leader

• Location: Gent, Belgium

About the job

Global Study Data Leader is responsible for leading the end-to-end data management activities and associated quality deliverables for clinical trials including study set-up, conduct, and close-out, complying with GCP and applicable regulatory guidance. Provide comprehensive data management expertise and support to team members. Coordinate cross functional teams globally to ensure the flawless conduct of a clinical trial. Ensure activities are completed according to agreed standards and timelines and serves as the Data Management representative in the study team.

Main responsibilities:

• Contributes to the implementation of department initiatives and objectives as well as cross-functional working groups. Implements and oversees processes and coordinates activities in conjunction with the internal team and Clinical Data Delivery Leader continually evaluates processes and applications for improvements.
• Oversee vendor activities to identify risks and ensure that activities are completed according to the SOW, regulations, and with expected quality. Implement quality control strategies and remediations as necessary.
• Ensure that all external data loading and integration activities (Incl. eCOA, IRT, central labs) are well established and that data is loaded as per study timelines (including transfer specifications and reconciliations).
• Ensure data quality by conducting and/or overseeing data management activities including validation, data review, and safety data reconciliation.
• Ensures an efficient implementation and follow-up of DM activities for outsourced trials.
• Develop and drive the retro planning for important deliverables such as Interim Analysis, DMC, partial, and final database locks.  Ensure clear and prompt updates and escalations to study teams and management. 
• Ensure Data base lock readiness by leading the team through the DM lock recommendations and rational, including implementation of Data Point Lock Strategy.
• Drive inspection readiness by ensuring ongoing TMF completion for all DM related documents (including documents coming from third parties if applicable).

About you

Education:

Bachelor’s degree or above, preferably in a life science or health related field or/and 8-10 years of Clinical Data Management in the pharmaceutical industry or equivalent can substitute a formal degree.

Experience:

• 5+ years of experience in Clinical Data Management in the pharmaceutical industry (or equivalent) is required.  2+ years of project management experience in Data Management is required. 
• Clinical Data Management System experience (CDMS) and understanding of
  database/programming concepts.
• Understanding of industry standards, terminologies, (e.g., CDISC SDTM, MedDRA, etc.)  current regulatory guidelines, and GCP practices regarding Data Management
• Vendor management
• Solid knowledge of the clinical trial development process
• Understanding of risk-based methodologies and regulations
• Experience using Data Visualization tools, e.g Spotfire, J-Review, Cluepoints preferred

Core knowledge, competencies & skills:

• Strong Data Management expertise i.e., understanding of Data Management scope and objectives.

• Solid knowledge of the clinical trial development process and understanding of relevant and current regulatory guidelines, Good Clinical Practice (GCP), industry standards, and practices regarding Data Management.
• Solid Clinical Data Management System experience (CDMS & EDC) and understanding of database development/programming concepts.
• Strong collaboration and interpersonal behaviors; manage activities effectively with study team and other DM functions. Establish rapport and collaborates inside and outside the company. Demonstrate flexibility through effective negotiations.
• Strong communication skills; Ensure clear, concise, consistent, and timely communication including risks identification, and escalation.  

Why choose us?

• Bring the miracles of science to life alongside a supportive, future-focused team.
• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
• Drive implementation science, powerful crowdsourcing and open innovation, discovering the ways to bring science to live faster, contributing to a patient first mindset
• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave

PursueProgress. Discover Extraordinary.

Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!