Principal Statistical Programmer

3 days ago

Remote, India Parexel Full time

As a member of Parexel’s Statistical Programming group, you will be heavily involved in leading trials to successful completion, working in close collaboration with sponsor teams, and Parexel teams in differing locations. Depending on your career goals, you will be provided the opportunity to be exposed to a variety of different sponsors, products and therapeutic areas, or choose to focus your career on working with a specific sponsor and gaining in depth knowledge of a specific therapeutic area and compound.

You will become a part of a team with an inherent breadth of knowledge and expertise in small, single center Investigator studies to multi-site, multi-national trials in Phases I to IV of clinical development, as well as observational studies. From initial planning meetings at the study design stage through to implementation and execution, our team of skilled statistical programmers will employ industry-accepted statistical tools and techniques, as well as innovative consulting, to provide the quality and efficiency of projects.

Parexel develops and delivers cost effective, high-quality training programs for those employees that are directly involved with sponsor functional partnerships to ensure that our statistical programmers can quickly step in to make significant contributions to the success of a study. In addition, you will receive the opportunity to shape your development through quarterly conversations with your manager. Explore opportunities within our core Clinical Development, Biotech, or Functional Service Provider (FSP) teams below.
- Full Time
- Travel: Minimal
- Glassdoor Reviews and Company Rating

**Success Profile**:
Check out the top traits we’re looking for and see if you have the right mix.
- Team player
- Tech-Savvy
- Communicator
- Proactive
- Detail-oriented
- Analytical

**Rewards**:

- **Global Impact**: We are one truly global team working together to propel each client´s journey ahead faster.
- **Balance**: We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
- **Development**: Opportunity to learn and grow through a performance and development goal-setting program.
- **Variety**: Opportunity to work on a wide range of therapeutic areas and medical devices.
- clinical project initiatives with a focus on programming and analysis reporting procedures.Education BA/BS/MS or international equivalent experience in statistics,(minimum/desirable): computer science, mathematics, life sciences or related fieldLanguages: Fluent English (oral and written).Experience/Professional requirement: 1. Advanced SAS experience and proven skills in the use of SAS within a Statistical Programming environment to develop and validate deliverables2. Advanced experience in contributing to statistical analysis plans and/or constructing technical programming specifications3. Good knowledge of industry standards including CDISC data structures as well as a solid understanding of the development and use of standard programs4. Good understanding of regulatory requirements relevant to Statistical Programming (e.g. GCP, study procedures).5. Good communications and negotiation skills, ability to work well with others globally6. Experience as Trial Programmer, including coordination of internal or external programmers on a given study/project7. Ideally 5+years of work experience in a programming role preferably supporting clinical trials/ or in pharmaceutical industry

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