Remote - Senior Clinical Data Analyst - Medical Device
Remote - Senior Clinical Data Analyst - Medical Device
Beacon Hill
United States
See who Beacon Hill has hired for this role
A highly reputable medical device corporation is currently hiring a Senior Clinical Data Analyst to work remotely in the United States.
Job Description:
- Designs clinical trial specific subject Case Report Forms for use in e-clinical EDC systems.
- Develops study specific annotated CRFs, database documentation, edit check specifications, data handling conventions and data entry instructions.
- Designs and validates clinical databases including designing logic checks, UAT etc.
- Knowledge of MedDRA and WHODrug Coding.
- Programs SAS edit checks and SAS macros for data cleaning.
- Processes clinical data including receipt, entry, verification and filing of information.
- Generates data queries based on validation checks or errors or omissions identified during data entry to resolve identified problems.
- Performs quality control audits to ensure accuracy, completeness, and proper use of clinical data system.
- Responsible for filing and maintaining CRFs, subject diaries, and other subject-specific documentation (e.g., Marketing questionnaires) collected during clinical studies.
- Responsible for filing and maintaining digital data collected during clinical studies.
- Summarizes basic elements for clinical databases periodically.
- Communicates with end users to define or implement clinical data management requirement for the clinical study such as data release, delivery schedules, and testing protocols.
- Provides training and technical support to clinical site personnel on EDC for specific studies.
- Maintains more than 3 study databases and data management activities concurrently.
- Ability to multi-task while still being detail oriented.
- Develops project-specific data management plans that address areas such as data reporting, transfer, database lock and work flow.
- Monitors work quality to ensure compliance with standard operating procedures.
Required Skills:
- Bachelor’s degree in a technical discipline, and a minimum of 5 plus years related experience or Master’s degree and 2 plus years equivalent industry experience or a PhD and 1 plus years of experience.
- Develops study specific CRF
- Programs SAS edit checks and SAS macros OR Strong EDC building experience
- Designs and validates clinical databases
-
Seniority level
Associate -
Employment type
Contract -
Job function
Quality Assurance, Research, and Finance -
Industries
Data Infrastructure and Analytics, Business Consulting and Services, and Biotechnology Research
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