Job details
Salary $84,404 - $156,456 a year job type full-time contract
Qualifications
Bachelor`s (preferred)
Benefits pulled from the full job description
Health insurance life insurance paid time off vision insurance
Full job description
Job title: cdm programmer ii - sas (amer) – remote
Location: wilmington, nc (remote )
Client: pharmaceuticals/cro
Description:
· 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 otherhealth related field or equivalent experience that provides the skills and knowledge necessary toperform 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 oradministration capacityOc/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 types: full-time, contract
Pay: $84,404.00 - $156,456.00 per year
Benefits:
Health insurance
Life insurance
Paid time off
Vision insurance
Schedule:
8 hour shift
Monday to friday
Covid-19 considerations:
Required fully vaccinated candidate
Application question(s):
Do you have medidata rave and/or rave certification?
Education:
Bachelor`s (preferred)
Experience:
Clinical trials environment: 2 years (required)
Oracle: 1 year (required)
Medidata rave: 1 year (required)
Work location: remote
Hiring insights
Hiring 10+ candidates for this role
Urgently hiring
Job activity
Employer reviewed job 1 day ago
Posted 30+ days ago
