Research Scientist Post for Biological Sciences Candidates @ Pfizer
This job expires in :
All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the bio pharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.
Job Title : Senior Clinical Programmer (Standards) – Research Scientist II
Reference : 4685568
Location : India – Chennai
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
Qualifications:
- 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
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