Senior Data Manager Job Description Template
Our company is looking for a Senior Data Manager to join our team.
Responsibilities:
- Develop processes and tools to monitor and analyze model performance and data accuracy;
- Utilize a variety of data visualization techniques to extrapolate data from PEO SOLDIER’s proprietary model;
- Develop custom data models and algorithms to apply to data sets;
- Define the software architecture of the growing data analytics capability;
- Coordinate with different functional teams to implement models and monitor outcomes;
- Develop Data Transfer Agreement(s) (DTAs) between external data vendors and/or core labs;
- Lead and Perform UAT of database and edit checks;
- Participate in the review of Clinical research documents (e.g., Protocols, Case Report Forms, Reports and Statistical analysis);
- Lead AE/SAE data reconciliation in Safety DB and/or other Data Management DB, including but not limited to, performing MedDRA and/or WHO coding;
- Coordinate and communicate with DB vendors on consistent basis to address Clinical team’s requests, project plans, and/or eCRF development activities;
- Has a good understanding of regulatory guidelines and issues (i.e., ICH GCP ), and understands the connection to DM deliverables;
- Leads the data review meetings with Medical, Clinical, Biostatistics and Programming in support of key reporting events or database lock plans;
- Identifies and implements process improvements in relation to data collection and processing;
- Uses metrics and key performance indicators (KPIs) to monitor vendor performance;
- Oversees multiple DM vendors and provides training as necessary.
Requirements:
- Excellent written and verbal communication skills;
- Programming and coding knowledge and experience with several languages: C, C++, Java, JavaScript, etc. a plus;
- Knowledge of advanced statistical techniques and concepts (regression, advanced statistical tests, etc.) and experience with applications;
- Knowledge and experience in statistical and data mining techniques;
- Strong problem-solving skills with an emphasis on product development;
- Applicants may be subject to a low-level government security investigation and must meet eligibility criteria for access to sensitive information;
- Participate in the review of Clinical research documents (e.g., Protocols, Case Report Forms, Reports and Statistical analysis);
- Lead AE/SAE data reconciliation in Safety DB and/or other Data Management DB, including but not limited to, performing MedDRA and/or WHO coding;
- Coordinate and communicate with DB vendors on consistent basis to address Clinical team’s requests, project plans, and/or eCRF development activities;
- Ability to multi-task and manage multiple priorities with minimum direction and supervision;
- Lead and Perform UAT of database and edit checks;
- Perform close-out audit, as specified, for closing of study trial in EDC or other clinical data management DBs;
- Five years of experience working with large datasets or databases. Experience should be in a professional working environment;
- Perform other activities as required;
- Develop Data Transfer Agreement(s) (DTAs) between external data vendors and/or core labs.