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Senior Clinical Trial Statistician
3 weeks ago
Job Opportunity: Statistical Data Analyst
">Sponsor-dedicated:
Working fully embedded within a global pharmaceutical client, with the support of our team behind you, you'll be at the heart of innovation. As a Senior Statistical Programmer you will be dedicated to one of our clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership.
Position Overview:
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.
Our Values:
- We believe in applying scientific rigor to reveal the full promise inherent in data.
- We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.
- We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
- We prize innovation and seek intelligent solutions using leading-edge technology.
Responsibilities:
How you will contribute:
- Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming.
- Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs).
- Production and QC/validation programming.
- Generating complex ad-hoc reports utilizing raw data.
- Applying strong understanding/experience of Efficacy analysis.
- Creating and reviewing submission documents and eCRTs.
- Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries.
- Performing lead duties when called upon.
- Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
- Being adaptable and flexible when priorities change.
Qualifications:
Here we want our employees to succeed, and we enable this success through consistent training, development and support. To be successful in this position you will have:
- Bachelor's degree in one of the following fields Statistics, Computer Science, Mathematics, etc.
- At least 7 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or equivalent. At least 5 years of related experience with a master's degree or above.
- Study lead experience, preferably juggling multiple projects simultaneously preferred.
- Strong SAS data manipulation, analysis and reporting skills.
- Solid experience implementing the latest CDISC SDTM / ADaM standards.
- Strong QC/validation skills.
- Good ad-hoc reporting skills.
- Proficiency in Efficacy analysis.
- Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials' data.
- Submissions experience utilizing define.xml and other submission documents.
- Experience supporting immunology, respiratory or oncology studies would be a plus.
- Excellent analytical & troubleshooting skills.
- Ability to provide quality output and deliverables, in adherence with challenging timelines.
- Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.
Benefits:
Our values drive our practices and assure all employees are trained properly, therefore they have the knowledge to do their job very well which in turn allows us to deliver high-quality results to our clients. Our qualified personnel help ensure the growth and success of our organization by dedicating themselves to the pursuit of excellence through ongoing learning and professional development. As a result, there will be continuous opportunities for career advancement and networking across different departments and industries. All our employees have competitive salaries, excellent health insurance options, and flexible work arrangements so they can manage their work-life balance easily. These benefits make it possible for our employees to advance their careers without compromising their personal lives. By combining innovation and commitment to quality, we attract talented individuals who are passionate about making a difference in their communities and industries. We appreciate all hardworking people like you
