Clinical Data Senior Database Programmer - REMOTE South San Francisco, California
Orbis Clinical is seeking a remote-based Senior Database Programmer for 12+ months.
Looking for an experienced Sr. Database Programmer who electronic data capture (EDC) database programming experience specifically in helping study team members optimize the use of Veeva CDMS to run successful clinical trials.
Job Description
- Work and consult with lead data managers, and study team members, as necessary, to review and understand clinical protocol requirements and all project specifications, applying industry and Veeva best practices
- Drive database development activities per implementation project plan by working with the lead data manager and study team members, as necessary
- Configure forms, rules, and other study items with Veeva CDMS during development
- Conduct user acceptance testing with the study team, including coordination of all feedback, resolution of issues, and acceptance of the study
- Support requirements gathering and specification creation process for all study integrations and go-live activities to ensure a smooth transition of the study to the study team
- Act as the study teams trusted advisor to ensure that the study trial design is configured to meet the team’s goals and offer full benefits of Veeva’s CDMS application while providing training and mentorship
- Communicate potential risks and contingency plans with the team’s requirements to ensure process compliance with all regulatory and procedural requirements
Requirements:
- 2+ years’ experience working with Veeva CDMS clinical software solutions in end-to-end data management related activities (database design, data collection, data analysis, query resolution and datasets)
- 5+ years’ experience in the life sciences industry and clinical trial processes (pharmaceutical, biotech, medical device companies, CRO’s, and academic & public health organizations) expertise in relation to design, documentation, and data collection
- Proven ability to work independently and collaboratively in a dynamic, fast-moving environment and meeting project timelines with quality results
- Excellent verbal and written communication, interpersonal, and presentation skills
- Working understanding of data management standards and guidelines (GCDMP, CDISC, SDTMIG, CDASH)
- Experience working with system integrators for IxRS, medical coding, local lab module and other clinical technologies
Orbis Clinical is looking for an experienced Sr. Clinical Database Programmer with electronic data capture (EDC) database programming experience specifically in helping study team members optimize the use of Veeva CDMS to run successful clinical trials. The role is remote-based for 12+ months.
What you’ll do:
- Work and consult with lead data managers, and study team members, as necessary, to review and understand clinical protocol requirements and all project specifications, applying industry and Veeva best practices
- Drive database development activities per implementation project plan by working with the lead data manager and study team members, as necessary
- Configure forms, rules, and other study items with Veeva CDMS during development
- Conduct user acceptance testing with the study team, including coordination of all feedback, resolution of issues, and acceptance of the study
- Support requirements gathering and specification creation process for all study integrations and go-live activities to ensure a smooth transition of the study to the study team
- Act as the study teams trusted advisor to ensure that the study trial design is configured to meet the team’s goals and offer full benefits of Veeva’s CDMS application while providing training and mentorship
- Communicate potential risks and contingency plans with the team’s requirements to ensure process compliance with all regulatory and procedural requirements
Requirements:
- 2+ years’ experience working with Veeva CDMS clinical software solutions in end-to-end data management related activities (database design, data collection, data analysis, query resolution and datasets)
- 5+ years’ experience in the life sciences industry and clinical trial processes (pharmaceutical, biotech, medical device companies, CRO’s, and academic & public health organizations) expertise in relation to design, documentation, and data collection
- Proven ability to work independently and collaboratively in a dynamic, fast-moving environment and meeting project timelines with quality results
- Excellent verbal and written communication, interpersonal, and presentation skills
- Working understanding of data management standards and guidelines (GCDMP, CDISC, SDTMIG, CDASH)
- Experience working with system integrators for IxRS, medical coding, local lab module and other clinical technologies
Compensation Details:
- Orbis Clinical provides a reasonable range of compensation for our positions. Actual compensation is influenced by a wide array of factors including, but not limited to, skill set, level of experience and specific office location.
- The Pay Range for this position is $95-$100 per hour, can vary depending on employment status.
- Orbis Clinical offers eligible employees health benefits (medical, dental, and vision), employer-paid basic life and AD&D insurance, and a partial employer match on a 401(k).
EEO and Reasonable Accommodation Statement:
Epic Staffing Group is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, genetic information, veteran status, or any other characteristic protected by law. We also consider qualified applicants with criminal histories, consistent with applicable law. If you need assistance or an accommodation during the application process, please contact us.
By applying for this position, you agree that any calls from Orbis Clinical and its subsidiaries may be monitored or recorded for training and quality assurance purposes.
