Hi,
-- We have an immediate need for RAVE Programmer/Study Builder. Please reply back with your resume if you are comfortable moving forward to shankar@sourceconsult.net or call 508-417-8385.
Location: Berkeley Heights, NJ
Duration: 6+ Months
Job Description:
Qualifications:
- Rave global library and edit check programming (including best practices, efficiencies and reusability).
- Develop, program, test and maintain global edit checks.
- Manages library studies and associated objects used for study configuration which have been approved through governance.
- Facilitates discussion for identification of objects which will be used for study configuration.
- Supports Disease Indication, Therapeutic and Franchise scientists from various therapeutic functions to proactively create new commonly used CRF's and edit checks which could be consumed by study.
- Helps Global Librarian to maintain various EDC libraries.
- Maintains consistency between Rave Libraries and MDR and/or other standards (if applicable).
- Interact with CPs to confirm understanding of Library for consistent study consumption.
- Liaison with the standard governance organization to maintain alignment with the business and proactively look for opportunities to build efficiencies.
- Manages risk mitigation, issue resolution and escalation related to Rave Global Libraries.
- Provide guidance for resolving Library capability concerns raised.
Qualifications:
- ***BASICALLY looking for a RAVE programmer.***
- Good communication skills-ability to work in a team environment with data managers, medical personnel, clinical monitors, statisticians, programmers.
- Strong adherence to timelines and comfortable with escalating deadlines if necessary.
- Must be comfortable with speaking up and applying their own experience of best practices.
- BS/BA degree or equivalent in a relevant scientific discipline with a minimum of five years' experience.
- Experience with one or more of Rave Modules: Coder, CSA, Patient Cloud, Safety Gateway, Site Payments, TSDV desired.
- Good communication skills; ability to work in a team environment with data managers, medical personnel, clinical monitors, statisticians, programmers, and medical writers.
- Knowledge of FDA/ICH guidelines and industry standard practices regarding programming.
- Medical or mathematics/computer science background a plus.
- Detailed knowledge and experience in case report form design, data validation.
- Knowledge of clinical trial design and basic statistics a plus.
- Experience in C# programming a plus.
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