Job Description
MedNova Clinical Analytics LLC is a dynamic and growing healthcare analytics and clinical research support company dedicated to serving pharmaceutical, biotechnology, and healthcare clients across the GCC and Europe. We are seeking a motivated and detail-oriented Statistical Programmer to join our innovative team. In this role, you will play a crucial part in supporting clinical trial programming, data analysis, and reporting activities, contributing directly to the success of our clients' research endeavors.
As a Statistical Programmer at MedNova, you will leverage your technical skills and understanding of clinical trial processes to develop and validate essential programming outputs. You will collaborate closely with a multidisciplinary team of biostatisticians, data managers, and project managers, ensuring the highest standards of data integrity and regulatory compliance. This is an excellent opportunity for a budding professional to gain extensive experience in a fast-paced, intellectually stimulating environment.
Requirements
Critical Requirements
- Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, Data Science, or a related quantitative field.
- 1-3 years of experience in statistical programming or clinical data analysis.
- Hands-on experience with SAS programming.
- Understanding of clinical trial data structures and processes.
- Familiarity with CDISC standards (SDTM and ADaM).
- Good analytical and problem-solving skills.
- Effective communication and interpersonal skills.
- Ability to work both independently and collaboratively within a team environment.
Important Requirements
- Experience with SDTM, ADaM, and Tables, Listings, and Figures (TLFs) development.
- Proficiency in performing dataset validation using tools like Pinnacle 21 Community.
- Experience reviewing study documents such as Protocols, Statistical Analysis Plans (SAPs), Case Report Forms (CRFs), and annotated CRFs.
- Experience in a Contract Research Organization (CRO) or pharmaceutical industry setting.
Nice to Have Requirements
- Exposure to Oncology or Ophthalmology clinical studies.
- Working knowledge of R, Python, SQL, or Power BI.
- Familiarity with regulatory and quality standards in clinical research.
About
MedNova Clinical Analytics LLC is a leading provider of advanced healthcare analytics and comprehensive clinical research support services. We partner with innovative pharmaceutical, biotechnology, and healthcare organizations to drive scientific discovery and improve patient outcomes. Our commitment to excellence, cutting-edge technology, and a collaborative work environment makes us a preferred partner for clients seeking to navigate the complexities of clinical research and data analysis.