Immediate Need for RAVE Programmer/Study Builder in Berkeley Heights, NJ
0 views
Skip to first unread message
shankar prasad
unread,
Jul 7, 2020, 12:50:27 PM7/7/20
Reply to author
Sign in to reply to author
Forward
Sign in to forward
Delete
You do not have permission to delete messages in this group
Copy link
Report message
Show original message
Either email addresses are anonymous for this group or you need the view member email addresses permission to view the original message
to sha...@sourceconsult.net
Hi,
We have an immediate need for RAVE Programmer/Study Builder. Please reply back with your resume if you are comfortable moving forward to sha...@sourceconsult.net or call 508-417-8385.
Location: Berkeley Heights, NJ
Duration: 6+ Months
Job Description:
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.