[ref. o84169102] Data Operations Manager
This position offers a long term contract employment opportunity.
Responsibilities:
We are seeking a self-motivated and skilled professional to provide support for our Digital Health Technology (DHT) wearable sensors and imaging components within clinical trials. This individual will play a crucial role in the set up, monitoring, and the data cleaning processes within our ongoing Biomeasures Endpoints and Study Technologies (BEST) projects.
Key Responsibilities:
- Act as principal contact for Operational and Vendor engagement.
- Contribute to overseeing and monitoring DHT-derived data.
- Collaborate closely with the data science team to track emerging data and verify the effectiveness of tools.
- Develop and implement operational plans to ensure complete data quality.
- Conduct data quality checks for ongoing projects.
- Collaborate with different stakeholders to adapt the project portfolio to changing needs.
- Contribute technical prowess to design and scale-up sensor systems.
- Ensure compliance with 21CFR part 11 guidelines in data collection, storage, and protection. • Recommend and implement improvements to existing data pipelines and workflows.
Qualifications:
- BA/BS degree in Health Informatics, Computer Science, Information Systems, or a similar field.
- At least three years of technical experience, including hands-on experience with Python, Unix/Linux environments, AWS or other cloud-based development, and EDC solutions e.g. REDCap, Encapsia, Oracle Clinical, Medidata Rave.
- Familiarity with pharmaceutical informatics standards like CDISC and MedDRA is preferred.
- Strong communication and collaboration skills and the ability to adapt to changing circumstances.
Preferred Experience:
- Masters degree in health informatics, computer science, information systems, or a similar scientific field.
- Previous involvement in Clinical Trials, processing large data sets from digital health technologies, and understanding of data structures, medical ontologies, interoperability standards, and data processing tools.
- Experience with SQL or NoSQL-based technologies.
Work Schedule: Monday to Friday, day shift.
Please note that a minimum of a BA/BS degree and three years of experience, including research or clinical trial experience is required. Familiarity with EDC solutions, pharmaceutical informatics standards like CDISC and MedDRA, and fulfillment of IRB/regulatory requirements is crucial for this role.