Not provided by employer
Description
Job summary
The clinical data manager performs functions related to data and information managementThis includes the management, coordination and documentation of data collection methods, change control, data security, and data retention within the project(s) task.
Responsibilities
Act as the project manager for stand-alone or multi-data management software application development project(s), effectively manage the activities of computer system development and validation life cycle and vendors in a manner that ensures all timeframes and targets are met with the highest quality to the company and sponsor’s satisfaction, and that costs are kept under control.
Provide clinical data management support to clinical operations team and/or study project, clinical data management team and biostatistics team
Participates in the review of clinical research documents (e.gProtocols, case report forms, reports and statistical analysis) provide leadership and guidance to data coordinators
Develop case report form (crf/ecrf), electronic and/or paper
Develops data transfer agreement(s) (dtas) between external data vendors and/or core labs.
Reconcile electronic data transfers from vendor to sponsor
Manage and update project timelines
Develop presentations and present at investigator meetings
Provide support and act as the data management point person to the sponsor, cros, vendors, clinical sites, and scorers
Creation, completion, organization, and tracking of all data management documentation
Assist in defining and/or create data listings, summary table validation, data specifications and/or process data transfers in preparation for statistical review and/or data management auditLead edc database (db) specification processDevelop test scripts and execution logs for user acceptance testing (uat).
Coordination of uat of ecrf build and validation documents, included but not limited to: edit check document, issue logs, uat summary reportPerform data review, query generation/resolution and data updates
Assist in defining and/or create data listings, summary table validation, data specifications and/or process data transfers in preparation for statistical review and/or data management auditTrain data coordinators on data qc procedures and edit checks for each study
Provide training and guidance to the srData coordinator and data coordinator (e.gData entry, oversight of data transfers, etc.) when needed/assigned
Collaborate with it and implementation team(s) to address clinical application requests and/or changes to clinical database systemsAssist in reconciling ae/sae data in safety db and/or clinical database
Coordinate the integration and reconciliation process that will be applied to external electronic data loads
Track study progress and issue periodic status reports as needed
Communicate with all operational departments regarding project status/issues
Follow and ensure compliance with good clinical practices (gcps)
Adhere to corporate policies and procedures
Other duties as assigned
Requirements
The position requires at least a bachelor’s degree with minimum of 5 years of experience in clinical data management in clinical trials.
In lieu of a bachelor’s degree a minimum of 6 years industry experience is required
At least 2 years of working experience on medidata rave platform, build edc in medidata rave or equivalent edc platform is preferred.
Experience of all data management processes from study start-up to study close-out
Knowledge of medical terminology, pharmacology, anatomy, and physiology.
Experience with at least one clinical data management system (cdms) including direct experience and/or understanding with database design, set-up and user acceptance testing; edit check development and/or programming and validation; management of data entry and queries; and study change control.
Data and computer system information management experience, medical terminology, relational database knowledge, programming experience (any language), and experience overseeing projects required.
Good communication, organization, and documentation skills are expected.
Good clinical practices training.
Hiring insights
Job activity
Posted 8 days ago
