DOCS provides global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical development industry.
Post : Clinical Statistical Programmer I
Job Description
• Solid work experience in a programming role supporting clinical trials in the pharmaceutical industry following standard operating procedures and working practices.
• Proven experience in supporting, or leading programming support for multiple clinical trials and submission activities (or equivalent).
• Proven experience in development of advanced MACROs (such as MACRO's to support analysis data set and TFL creation) with high programming efficiency; strong programming and problem-solving skills.
• 3+ years work experience in a programming role preferably supporting clinical trials/ or in the pharmaceutical industry following standard operating procedures and working practices.
• Advanced knowledge of experience with SAS and other relevant programming software.
• Experience in developing Safety datasets and TFLs in line with sponsor specifications. Should have worked on development/validation of all complex safety datasets such as ADLB, ADAE, ADEG, etc.
• Should possess complex dataset programming.
• OPTIONAL: CRT tasks – Define.xml , Data derivation document creation, etc or Pooling submission for safety, efficacy
Additional Information
Experience : 3+ years
Ref #: 16001
Location : Bangalore/ Chennai
Industry Type : Pharma/ Healthcare/ Clinical research
Employment type: Permanent - Full-Time
End Date : 5th January, 2020
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