Clinical Programmer in Berkeley Heights, NJ at Pyramid Consulting, Inc

Date Posted: 11/14/2019

Job Snapshot

Job Description

Immediate need for a talented Clinical Programmer with experience in the Pharmaceuticals Industry.
This is a 12+ Months Contract opportunity with long-term potential and is located in Berkeley Heights, NJ. Please review the job description below.
Job ID: 19-51670
  • Oversee and monitor CRO DB Build (in Medidata Rave) to ensure that Client standards are implemented in all studies.
  • Schedule and lead eCRF design meetings.
  • Routinely interface with cross-functional team members.
  • Proper management of project priorities and timelines required.
  • Review clinical programming activities and costs in contracts.
  • Develop, program, test and maintain clinical trial databases and data entry screens using Medidata Rave in accordance with Client standards.
  • Review validation/edit checks for in-house and outsourced studies.
  • Act as liaison with vendors and oversee CRO to establish external data transfer specifications
  • Retrieve data from CRO and external vendors.
  • Develop, program, test and maintain data review listings in Jreview and/or SAS for data review purposes.
  • Provide technical expertise and support to Data Management team.
  • Make data available to company personnel and regulatory agencies when required
  • Perform post processing of data extracts in accordance with Client standards to be delivered to Biostatistics (if in-house study)
  • Coach and advise junior programmers to identify problems and solutions.
Key Requirements and Technology Experience:
  • BS/BA degree or equivalent in a relevant scientific discipline with a minimum of five years experience.
  • Detailed knowledge and experience in case report form design, central laboratories, programming databases, query resolution, data validation.
  • Advanced knowledge of clinical database design is a MUST (Medidata Rave experience is most important.
  • Inform and Oracle Clinical or other systems are of lesser importance).
  • Good communication skills is a must
  • 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
  • Knowledge of SQL and SAS programming.
  • Knowledge of clinical trial design and basic statistics (a plus).
Our client is a leading Pharmaceuticals Industry and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.