What are the responsibilities and job description for the Clinical Data Programmer I position at Invicro?
Clinical Data Programmer I – Remote
Overview:
The Clinical Data Programmer provides advanced data management support to internal study and scientific teams. This is a technical role involving both advanced software capabilities and a strong understanding of good clinical data management practices. This position supports deployed software applications in a regulated environment and their use within Invicro Data Management and across other research areas of the organization.
Essential Functions:
- Develop data collection forms to maximize efficiencies in data acquisition across multiple imaging modalities and therapeutic areas.
- Programming data cleaning/consistency checking programs to support internal applications for all therapeutic areas
- Programming and testing data export programs in accordance with specific client needs
- Design and develop custom calculations, error checks, and automated data validation routines.
- Build data conversion paths and develop efficient and appropriate sponsor deliverable file formats, including CDISC SDTM and ODM compliance requirements
- Assist with the development of data integrations for continuity across internal data platforms (sites, sponsors, Invicro locations)
- Provide coaching, support and mentoring to less experienced team members in data management practices and related technical issues
- Support DM personnel in the development of technical documentation
- Advise on the development of database quality standards including the oversight of standard eCRF library and version control processes.
- Other duties as assigned.
Qualifications:
- Bachelor’s Degree in mathematics, computer science or equivalent demonstrated technical and analytical experience.
- 1-2 years’ experience in data management
- Strong documentation and reporting capabilities.
- Detail oriented self-learner capable of training those in use of data analytics and data management practices.
- Possess strong written and verbal skills for effectively communicating with departmental staff and research centers.
- Experience implementing CDISC standards
- Understanding of GxP
- Understanding of 21 CFR Part 11
- Median level SAS programing experience
- Experience with EDC (e.g. Open Clinica, RAVE, Inform, TrialMaster, etc.)
- Entry level SQL proficiency
- Entry level Javascript proficiency
Invicro is an Equal Opportunity Employer. We maintain a drug-free work environment. All qualified applicants will receive consideration for employment without regard to actual or perceived race (and traits historically associated with race, including, but not limited to hair texture and protective hairstyles such as braids, locks, and twists), color, creed, religion, citizenship status, sex or gender (including pregnancy, childbirth and related medical conditions), parental status, sexual orientation, gender identity, gender expression (including transgender status), national origin, ancestry, age, marital status or protected veteran status and will not be discriminated against on the basis of physical or mental disability, protected medical condition as defined by applicable state or local law, genetic information, political affiliation or any other characteristic protected by applicable federal, state, or local laws and ordinances.
Invicro does not accept unsolicited resumes from individual recruiters, third party recruiting agencies, outside recruiters or firms without an executed contract in place. We are not responsible for any fees related to resumes that are unsolicited or are received by Invicro. Such resumes will be deemed the sole property of Invicro and will be processed accordingly.
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