Covance

Programmer Analyst

Job Location(s) IN-Bangalore
Job Number
2021-65162
Job Category
Clinical Data Management
Position Type
Full-Time
Telecommute
Yes

Job Overview

- Performs independent programming activities on multiple projects concurrently with less or no support from Senior Programmers. Development and implementation of solutions to global technical service issues and concerns regarding EDC tools like Medidata RAVE or Oracle InForm or SAS programming
- Read understand requirement documents/Specifications, database design/SAS programming, Reports design and conduct quality control processes including database review to meet client requirements.
- Program ad-hoc/scheduled reports using SAS/Cognos/Business Objects – XI /R and other tools for data cleaning and reporting
- Perform any post production changes, publish checks, complex structure dynamics, Rave Safety Gateway, Balance (RTSM) mapping setting to the EDC database or enhancements to the SAS programs like SAS edit checks, listings, Protocol Deviations, etc
- Complete assigned work utilizing EDC tools or SAS or other proprietary software according to Labcorp Drug Development SOPs, Work Instructions and Instructions, project and project specific guidelines in accordance with Good Clinical Practices
- Train and mentor the team on EDC tools or SAS as required and have them ready to perform independent enough on day to day activities.
- Perform quality check and ensure the work is delivered with 100% quality and with knowledge of regulations pertaining to computerized systems to ensure compliance
- Continuously learn and improve communication, technical and problem-solving skills.
- Interact with project team members in related discipline and provide solutions to the operational issues.
- Able to work independently on multiple sponsors and take initiative to accept new challenges in Clinical Programming Applications
- Reconcile database build, project files, reports, listings and other documents related to programming for accuracy, completeness of Data Management processes
- Work in a timely manner in accordance with all the activities specified in the agreed study budget, under the supervision of Sr. Programmers.
- Perform other duties as assigned by Manager

Education/Qualifications

BE - Comp.Science, Information Technology, MCA with relevant Clinical SAS experience. Good to have SAS certification but not mandatory.

Experience

 
- 3 - 6 years of relevant work experience to include data management and database support: SAS programming.
- Good problem solving skills and a proactive approach
- Good oral and written communication skills
- Good knowledge of clinical trial process and data management, biometrics, and systems applications to support operations preferred
- Ability to work in a team environment
- Ability to work effectively under minimal supervision
- Ability to prioritize work and Self-motivation
- Good time management skills and the ability to work to tight deadlines whilst maintain the highest standards of quality work
- A cooperative and team-oriented approach

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