Job Details

Responsibilities:

• Lead the data quality evaluation by investigating all clinical and operational data, evaluating trends, deviations, using visual analytics tools and ad hoc reports.
• Manage high complex studies and support specific activities of studies managed by other data managers or consultants
• Provide technical tutoring and supervise data managers and/or contractors assigned to clinical studies by conducting regular reviews of activity status
• In-depth knowledge of Clinical Data Interchange Standards Consortium (CDISC) relating to data standards including Study Data Tabulation Model (SDTM) and Case Report Tabulation Data Definition Specification (Define.xml)
• Manage and guide providers, setting requirements, preparing or reviewing Request for Proposals and monitoring performance.
• Regularly monitor data management costs of the assigned studies ensuring respect of budget.
• Define and proactively manage risks with potential impact on study systems setup, study conduction, or reliability of study results
• Ensure all data collection systems for assigned projects are setup, tested and fit for purpose according to expectations and timelines
• Define the strategy and lead the preparation of data package for regulatory submission
• Represent data management for auditing and regulatory inspection
• EHR data, data collected directly from patients, omics data, other secondary data)
• dvanced analytical and technical skills to interrogate and mine high volumes of data from a variety of sources.

• Minimum 8+ years of experience in Clinical Data Management in CROs or Pharmaceutical Industry
• Solid knowledge of drug development processes
• Strong data management expertise
• Excellent knowledge of Good Clinical Data practices, GCP and regulatory requirements
• Experience with clinical databases, electronic data capture (EDC) systems, wearables, and sensors to collect data directly from patients
• Excellent knowledge of Risk-Based approach
• Knowledge of Real-World data sources and processes to collect/manage different types of sources.
• Basic knowledge of Artificial Intelligence (AI)
• Project Management skills
• Excellence in planning and priorities setting
• nalytical, problem-solving skills and ability to take ownership of decision-making
• Strong commitment to quality
• Excellent oral and written communication and presentation skills
• bility to collaborate and work in a team-based environment
• Courage, resilience, and ability to adjust to a rapidly changing environment
• Experience with Medidata platform
• Familiarity with other platforms for secondary data
• Proficiency in SAS Systems.