What are the responsibilities and job description for the Sr. Clinical Data Manager position at Katalyst CRO?
Responsibilities
This position is responsible for data management activities, including developing data management plans, validating/testing databases, defining specifications to review data (manual, automatic (EDC edit checks), and SAS validations), and reviewing/tracking clinical trial data to ensure the completeness, accuracy, and consistency of the data collected during clinical trials
Study Specific Activities.
Coordinate and complete data management activities to meet project timelines and communicate status to clinical project managers.
Develop study specific data management plans and case report form (CRF) completion guidelines.
Review and approve documents associated with data collection: CRFs, edit checks, data handling conventions, and data entry instructions.
Review and finalize clinical study database validation plans, lead the database validation team, and ensure all documentation is completed prior to GO-LIVE.
Complete data verification process (i.e., issue data clarification forms (DCFs) for paper CRFs or issue queries for EDC).
Review completed DCFs and/or queries to ensure data discrepancies are resolved in the database.
Prepare electronic data transfer protocols and coordinate data transfers (imports and exports) with third party vendors and consultants and Project Biostatisticians.
Lead database cleaning and lock activities, coordinating data transfer reconciliation, serious adverse event reconciliation, and database audits with QA or data quality reviews with another Clinical Data Manager.
Ensure all study specific documentation is filed appropriately in the study-specific Trial Master File.
Manage and prioritize data management activities to meet project schedules.
Report on required data management metrics to ensure efficient review of data.
Develop data management resource forecasting and tracking model to assist with project planning and support.
Optimize database development and validation processes to improve departmental efficiency.
Train and mentor Clinical Data Associate(s) to develop clinical data review and other technical data management skills.
Requirements
Bachelor's degree in a scientific discipline, at least 3 years of clinical data management experience in the pharmaceutical/biotechnology industry.
More experience will be required for a senior level CDM candidate.
You must be highly detail-oriented while still maintaining work efficiency, be able to prioritize activities and multi-task across various projects that will be at different study stages.
We prefer you to have MedDRA and WHO Drug coding proficiency.
This position is responsible for data management activities, including developing data management plans, validating/testing databases, defining specifications to review data (manual, automatic (EDC edit checks), and SAS validations), and reviewing/tracking clinical trial data to ensure the completeness, accuracy, and consistency of the data collected during clinical trials
Study Specific Activities.
Coordinate and complete data management activities to meet project timelines and communicate status to clinical project managers.
Develop study specific data management plans and case report form (CRF) completion guidelines.
Review and approve documents associated with data collection: CRFs, edit checks, data handling conventions, and data entry instructions.
Review and finalize clinical study database validation plans, lead the database validation team, and ensure all documentation is completed prior to GO-LIVE.
Complete data verification process (i.e., issue data clarification forms (DCFs) for paper CRFs or issue queries for EDC).
Review completed DCFs and/or queries to ensure data discrepancies are resolved in the database.
Prepare electronic data transfer protocols and coordinate data transfers (imports and exports) with third party vendors and consultants and Project Biostatisticians.
Lead database cleaning and lock activities, coordinating data transfer reconciliation, serious adverse event reconciliation, and database audits with QA or data quality reviews with another Clinical Data Manager.
Ensure all study specific documentation is filed appropriately in the study-specific Trial Master File.
Manage and prioritize data management activities to meet project schedules.
Report on required data management metrics to ensure efficient review of data.
Develop data management resource forecasting and tracking model to assist with project planning and support.
Optimize database development and validation processes to improve departmental efficiency.
Train and mentor Clinical Data Associate(s) to develop clinical data review and other technical data management skills.
Requirements
Bachelor's degree in a scientific discipline, at least 3 years of clinical data management experience in the pharmaceutical/biotechnology industry.
More experience will be required for a senior level CDM candidate.
You must be highly detail-oriented while still maintaining work efficiency, be able to prioritize activities and multi-task across various projects that will be at different study stages.
We prefer you to have MedDRA and WHO Drug coding proficiency.
Clinical Data Specialist
Vanguard Clinical -
San Diego, CA
Sr. Data Product Manager
ResMed -
San Diego, CA
Sr. Clinical Project Manager
Therapeutics Inc. -
San Diego, CA
