Clinical Trials Data Specialist
5 days ago
Job Overview
Fortrea is seeking an experienced Clinical Trials Data Specialist to join our sponsor-dedicated Flexible Solutions business unit. As a key member of our global project team, you will be responsible for developing and validating SAS programs for data presentations and analyses.
The ideal candidate will have a strong background in statistical programming, with experience working on complex clinical trials (phases I-III) and ADaM datasets. You will also have a solid knowledge of CDISC standards and prior experience working on oncology data or vaccine trials.
About the Role
- Develop and validate SAS programs for data presentations and analyses
- Provide programming support to the global project team
- Collaborate with cross-functional teams to deliver high-quality results
- Maintain awareness of industry standards, global regulatory requirements, and internal guidelines
- Identify opportunities to improve efficiency, quality, and productivity of our clinical statistical programming business
In this role, you will work on complex projects, lead studies through various phases of the clinical development plan, and support submissions, regulatory questions, publications, and ad hoc requests.
Your Profile
- Degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc.
- Solid professional experience as a statistical programmer within a biotech, CRO, or pharmaceutical company
- Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs
- Proven professional experience with SDTMs, ADaM datasets (safety and efficacy), and TFLs
- Solid knowledge of CDISC standards
- Prior experience working on oncology data (safety and efficacy) and/or on vaccine trials
- Strong organizational skills, autonomous and collaborative work style, curious mind, and keen attention to detail
- Business fluency in English - both spoken and written - is a must
As a valued member of our team, you will enjoy a highly competitive compensation package, including local benefits, flexible working hours, thorough onboarding, and excellent training and career development opportunities.
Benefits
- Rewarding and meaningful work in an established, diverse, highly profitable, and respected global company
- Highly competitive compensation packages, including various local benefits
- Genuine work-life balance
- Flexibility in working hours
- A thorough onboarding with support from your personal mentor
- A permanent employment contract with Fortrea
- Excellent training and career development opportunities
- Strong support from your Line Manager and your team, as well as from more than 20,000 Fortrea colleagues worldwide
Salary
The estimated salary for this position is between $90,000 and $120,000 per year, depending on location and experience.
About Fortrea
Fortrea is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.
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