Programmer
2 weeks ago
Labcorp Drug Development
As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.
Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical and regulatory expertise.
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Development and implementation of solutions to global technical service issues and concerns regarding EDC tools like Medidata RAVE, Oracle InForm and SAS programming.
- Read, understand and program EDC objects/SAS programming as per the specification documents which meets client requirements and projects.
- Perform any post production changes to the EDC data base or enhancements to the SAS programs like SAS edit checks, listings, Reconciliation listings, Protocol Deviations, ACDR listings etc.
- Perform publish checks, complex structure dynamics, RSG, Balance mapping settings.
- Complete assigned work utilizing Medidata RAVE or Oracle InForm or SAS or other proprietary software according to Covance SOPs, Work Instructions ,and project specific guidelines in accordance with Good Clinical Practices
- Provide suggestions and solutions to the operational issues.
- Perform quality check and ensure the work is delivered with 100% quality.
- Prioritize personal workload to meet specified completion dates and perform work with supervision and direction from managers.
- Maintain study databases for assigned projects and SAS programming as assigned by managers.
- Perform all work with knowledge of regulations pertaining to computerized systems to projects to ensure compliance.
- Ensure quality of personal work
- Interact with project team members in related discipline e. g. Clinical Data Management, Clinical Operations and Data Management.
- Display a positive attitude at all times, promoting and contributing to good team spirit in a professional environment
- Continuously learn and improve communication and technical skills.
- Attention to detail is essential and all tasks must be carried out to the highest standard.
- Develop good problem solving skills and a willingness to learn and seek advice from senior Programming staff
- Acquire knowledge of other aspects of the work of Programmer/Analyst under the supervision of the senior Programming staff
- Carry out all activities according to Covance SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP).
Perform other duties as assigned by Manager.
**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
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