Lead Clinical Data Manager
Katalyst Healthcares & Life Sciences
Behavioral Health Market Context
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Job Description
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)
• Advanced analytical and technical skills to interrogate and mine high volumes of data from a variety of sources.
Requirements:
• 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.
• Analytical, problem-solving skills and ability to take ownership of decision-making.
• Strong commitment to quality.
• Excellent oral and written communication and presentation skills.
• Ability 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 System.
• 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)
• Advanced analytical and technical skills to interrogate and mine high volumes of data from a variety of sources.
Requirements:
• 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.
• Analytical, problem-solving skills and ability to take ownership of decision-making.
• Strong commitment to quality.
• Excellent oral and written communication and presentation skills.
• Ability 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 System.
Qualifications
- •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
- •Analytical, problem-solving skills and ability to take ownership of decision-making
- •Strong commitment to quality
- •Excellent oral and written communication and presentation skills
- •Ability 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 System
Benefits
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)
- •Advanced analytical and technical skills to interrogate and mine high volumes of data from a variety of sources
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