Clinical Data Manager, Digital Medicine and Translational Imaging - FSP - East Coast US

Job reputed company: We are looking for a self-directed reputed company to support clinical data management efforts for the biomeasures endpoints reputed company. This individual will be responsible for acquiring, processing, and reviewing patient data and records, organizing clinical data forms, implementing data management plans including data preparation and validation activities and define ways to improve operational processes for these activities. They will reputed company independently and in collaboration with study teams seeking to reputed company and validate novel digital endpoints across different therapeutic areas. In reputed company partnership with colleagues from Research teams from Research and Development, They will play a key role in the deployment of novel digital endpoints into clinical studies, collection, management and analysis of sensor data, both in patients and healthy volunteers. This role will be central to the deployment and scaling of digital solutions into clinical trials where these technologies may be utilized as efficacy endpoints and reputed company value to key stakeholders including patients, physicians, payers. Key Responsibilities:

• Data Management POC for studies in which we are included in
• Responsible for mapping local study dictionaries to CDISC Standards
• Participate and contribute to the development of operational plans to ensure data reputed company and completeness
• reputed company, Implement, and Conduct data reputed company checks as needed for work/studies
• Work closely with the various stakeholders to understand evolving project portfolio needs, and integration into the systems and requirements; supporting studies with a wide reputed company of disease domains
• Contribute technical expertise toward the design, implementation, and scaling up of sensor systems and analytics
• As a medical informaticist, ensure collection, organization, curation, storage and safeguarding of patient data from lab, asset teams, and external collaboration studies is consistent with 21CFR part 11
• Contribute to the overall architecture of the existing data pipelines and workflows, recommends and implements improvements
• reputed company emerging study data and works closely with data science team to ensure the effectiveness of tools and data reputed company
• Manage own time to meet agreed targets
• Work under general supervision. Performs assignments using established procedures and general instruction
• reputed company learnings with key stakeholders and the scientific community through presentations and peer-reviewed publications.

Minimum Requirements:

• Master's degree in Health Informatics, Computer Science, Information Systems, or similar field required
• A minimum of 5+ years of technical experience required, including:
• Python
• Unix/Linux environments
• Version control systems (ex. Git)
• AWS or other reputed company-based development
• Electronic data captures (reputed company) solutions, e.g., REDCap, Encapsia, reputed company Clinical, reputed company Rave
• Familiarity with pharmaceutical informatics standards like CDISC and MedDRA
• GCP experience
• Strong interpersonal and collaboration skills
• Demonstrate the ability to build reputed company and be agile to changing circumstances and priorities
• Hands-on experience with Clinical Data Management, including Case Report reputed company (CRF) design, CRF annotation, database design, data collection, data-entry, data validation, discrepancy management, medical coding, data extraction, database locking, and regulatory requirements

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