CDM Programmer II, SAS (REMOTE) - a global LifeSciences leader!

Published date Posted on Indeed on Oct 11, 2021 (5 d ago)

REMOTE Opportunity:
The CVs that are shared predominately have candidates with SDTM/Statistical programming experience, but it would be helpful if we can get candidates with experience in Clinical SAS programming.
Listings: Needs to work on the Clinical Listings programming.
Listings: Working on Recon listings by importing of the clinical SAS datasets into the SAS Environment
Data Imports: which includes importing of the 3rd party vendor data and data transfers.
Data Imports: Creation of the data Import Agreements for 3rd party Vendor data

Database position working with clinical trials data systems under general supervision. Provides technical
leadership for some or all of the following activities: Designs and implements global library and study
specific setup for clinical trials applications; develops and validates data checks; provides first-line enduser
support/problem solving; provides support for application validation activities.

  • Serves as Technical Lead on Study specific database design / build activities adhering to the timelines established by the project team and indicated by the contract.
  • Reviews designs for compliance/feasibility within the database system and consistency with any current standards and/or sponsor specification and meets with study teams on a regular basis during initial study setup to ensure effective communication and accuracy in design
  • Develops and validates data checks and performs core setup and supports processes for various peripheral systems
  • Coordinates the activities of other Database Programmers that might assist in building studies to ensure all jobs are carried out and timelines are met.
  • Updates annotations and production databases where required based on protocol amendments or other changes to trial designs within timelines as agreed with project team
  • Provides basic technical support / consultancy and end-user support
  • Works with IT in troubleshooting, reporting and resolving system issues

Minimum Required Education and Experience:
Bachelor's degree in computer science, statistics, biostatistics, mathematics, biology or other
health related field or equivalent experience that provides the skills and knowledge necessary to
perform the job.
Minimum of 2 years experience in a clinical trials environment or similar field
Minimum of 1 years experience with Oracle or similar applications in a programming or
administration capacity. OC/RDC experience preferred.
Minimum of 1 year experience with Medidata Rave and/or Rave certification
Required Knowledge, Skills and Abilities:

Good organizational skills with the ability to adapt and adjust to changing priorities and to
manage multiple assignments with challenging/conflicting deadlines.
Good computer skills
Knowledge of relational database systems (RDBMS) and structure

Experience in Oracle and with Oracle tools or similar, with working knowledge of SQL and/or
PLSQL
Strong attention to detail and problem solving skills
Good written and verbal communication skills
Demonstrated experience in identification and resolution of technical problems in a professional
environment
Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data
Ability to attain, maintain and apply a working knowledge of GCPs and applicable SOPs
Demonstrated positive attitude, enthusiasm toward work, and the ability to work well with
others.

Job Type: Full-time

Benefits:

  • Dental insurance
  • Health insurance
  • Paid time off
  • Vision insurance

Schedule:

  • Monday to Friday

Experience:

  • SQL: 1 year (Preferred)
  • Informatica: 1 year (Preferred)
  • Data warehouse: 1 year (Preferred)

Work Location:

  • Fully Remote

Work Location: Remote


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