Clinical Data Manager Avid Radiopharmaceuticals
Department: Clinical Operations
Job Title: Clinical Data Manager
Reports To: Senior Director, Clinical Operations
Avid Radiopharmaceuticals, Inc. (Avid RP), a wholly owned subsidiary of Eli Lilly and Company, is a molecular imaging company developing novel PET imaging agents with the potential to aid in diagnosis, treatment selection and therapeutic monitoring of serious diseases. For more information, visit www.avidrp.com.
The Clinical Data Manager is responsible for providing Clinical data management support to Clinical Operations team and/or study project, Clinical Data Management team and Biostatistics team.
Oversees data management work performed by third parties,
Participates in the review of Clinical research documents (eg. Protocols, Case Report Forms, Reports and Statistical analysis).
Develops Data Management Plan (DMP), maintains DMP throughout lifecycle of study project and ensures DMP is followed according to study design and requirements.
Develops Case Report Form (CRF), electronic and/or paper.
Develops database (DB) clinical trial data specifications, including eCRF design, user requirements, edit rules/checks, query logic and data validations.
Leads EDC database (DB) specification process.
Develops Data Transfer Agreement(s) (DTAs) between external data vendors and/or core labs.
Reconcile electronic data transfers from vendor to Sponsor.
Develop 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 report.
Maintenance/tracking of EDC user management and other Clinical databases across allocated Clinical trials, including but not limited to, compiling master user lists and activating/deactivating user accounts.
Perform training on study trial for EDC and create user guides.
Ensure clinical data within EDC is in quality to lock/unlock and freeze/unfreeze as appropriate for statistical review, interim review, and or final database lock- included but not limited to: data reconciliation and/or coding.
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 audit.
Coordinate the archiving of study databases and related documents.
Perform close-out audit, as specified, for closing of study trial in EDC or other clinical data management DBs.
Assist in reconciling AE/SAE data in Safety DB and/or other Data
Management DB, including but not limited to, performing MedDRA and/or WHO coding.
Assist and provide input into study and project level data analysis plan.
Coordinate and communicate with DB vendors on consistent basis to address Clinical teams requests, project plans, and/or eCRF development activites.
Collaborate with IT and implementation team(s) to address Clinical application requests and/or changes to Clinical database systems.
Participates in the preparation and presentation of data, when applicable.
Ensures data system compliance by following the established guidelines of national and international regulatory authorities.
Bachelor?s degree in a science related field.
At least five (5) years data management and/or related work experience in a medical device or pharmaceutical industry/company.
Working knowledge of Good Clinical Practices, Clinical research, Clinical trial process and related regulatory requirements and terminology.
Working knowledge of Clinical database applications.
Excellent verbal and written skills, good organizational, interpersonal, and team skills.
Applicable knowledge working with other clinical databases such as Oracle Clinical, SAS, other.
Experience with working on Phase I- IV study trials within the medical device and/or pharmaceutical industry.
AE Coding, if applicable.
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