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Clinical Programmer - SAS, Rave in Berkeley Heights, NJ at APEX Systems

Date Posted: 4/15/2019

Job Snapshot

Job Description

Job #:  960355

Responsibilities: 

  • Review computer validation/edit checks for in-house and outsourced studies 
  • Develop, program, test and maintain computer validation/edit checks SAS 
  • Develop, program, test and maintain data review listings in Rave, Jreview and/or SAS for data review purposes 
  • Perform external data loads, i.e., labs, ECGs, etc., as needed. Act as liaison with vendors to establish transfer specifications and Celgene standards 
  • Validate peer programming 
  • Participate in and lead team meetings when appropriate 
  • Act as primary CRO contact, when necessary, to ensure that Celgene standards are implemented in all studies 
  • Provide technical expertise and support to Data Management team 
  • Make data, including interim data, available to company personnel and regulatory agencies when required 
  • Perform post processing of data extracts in accordance with Celgene standards to be delivered to Biostatistics 
  • Routinely interface with cross-functional team members 
  • Influences other functions and represents as DBO technical expertise 
  • Internal team leader who decides best course of action 
  • Coach and advise junior programmers to identify problems and solutions 
  • Manage outside CROs and consultants: 
  • Review clinical programming activities and costs in contracts 
  • Interact with CROs in the design and development of databases that are compatible with company needs 
  • Monitor progress of clinical programming activities in CROs 
  • Participate in regular team meetings and provide input when appropriate 
  • Participate in the development of clinical programming SOPs and the development/optimization of clinical programming processes from study start up to database lock. 
  • Routine interface with cross-functional team members in creating an appropriate database, data quality assurance, and support of data cleaning activities 
  • Managing project priorities and timelines 

Qualifications: 

  • BS/BA degree or equivalent in a relevant scientific discipline with 5+ years experience 
  • Advanced knowledge of clinical database design is a must (Rave).
  • Participation in at least one NDA is preferred 
  • 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, central laboratories, programming databases, query resolution, data validation 
  • Knowledge of SAS programming desired
  • Computer skills: detailed knowledge of clinical database design (Rave), proficiency with SAS data sets and conversion procedures, knowledge of MS Office program suite 
  • Knowledge of clinical trial design and basic statistics a plus

***For immediate consideration, please email your updated resume to woodbridgels@apexlifesciences.com with 'Clinical Programmer' in the subject line.

 

 

 

 

 

 

 

 

EEO Employer

Apex is an Equal Employment Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law. Apex will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation in using our website for a search or application, please contact our Employee Services Department at 844-463-6178