Opportunity for Senior Clinical Programmer at Pfizer

Pfizer is the world's premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support. At Pfizer, colleagues in more than 90 countries work every day to help people stay happier and healthier longer and to reduce the human and economic burden of disease worldwide.

Post : Senior Clinical Programmer (Standards) - Research Scientist II

Job Description
ROLE SUMMARY:
• A highly productive, independent programming lead ensuring excellence in the delivery of clinical and data management ad hoc listings
• Ensures excellence in the programming of analysis ready datasets, tables, listings, and figures for which they are responsible
• Ensures adherence to high quality programming standards in their daily work

Responsibilities:
• Accountable for the quality and timely delivery of enterprise, study and asset level deliverables of standard and ad hoc clinical listings
• Experience extracting data from EDC systems (i.e., OC/RDC, InForm, or Rave)
• Experience with JReview and SpotFire is required
• Works with clinicians, statisticians, data managers, programming resources and other colleagues as appropriate to ensure clear specifications for programmed deliverables are in place
• Exhibits routine and occasionally complex problem solving skills, seeking direction when appropriate
• Works with statisticians and programming leads to ensure clear specifications for their programmed deliverables are in place.
• May contribute to department level initiatives

Candidate Profile
• Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field
• At least 3 years of hands-on clinical programming experience working with SAS, JReview and Spotfire within a pharmaceutical, biotech, CRO, or Regulatory Agency
• Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial data
• Good understanding of ICH and regulatory guidelines
• Working knowledge of clinical data and relevant data standards
• Strong written and oral communication skills, and project management skills
• Proven ability to operate with limited oversight
• Proven ability to manage delivery under tight timelines

Additional Information
Qualification : Bachelor or Master (preferred) Degree
Experience : 3 years
Location : Chennai
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 30th September, 2018