Parexel yangi dori vositalarini ishlab chiqish jarayonida biofarmatsevtika kompaniyalariga xizmat ko‘rsatuvchi global klinik tadqiqot tashkilotidir. Uning faoliyati I–IV bosqich klinik sinovlari, portfel va tadqiqotlarni boshqarish, tartibga solish strategiyasi, bozorga chiqish hamda hayotiy siklni rejalashtirishni qamrab oladi. 21 000 dan ortiq mutaxassisga ega Parexel klinik, tartibga solish va terapevtik tajribani bemorlar haqidagi tushunchalar hamda innovatsion sinov dizaynlari bilan birlashtiradi. Kompaniya onkologiya, neyrofanlar va kam uchraydigan kasalliklar kabi yo‘nalishlarda tadqiqotlarni qo‘llab-quvvatlaydi hamda klinik ishlab chiqish jarayonini samaraliroq va bemorga yo‘naltirilgan qilishga e’tibor qaratadi.
Clinical Data Analyst II at Parexel – Hyderabad Hybrid
Support Parexel clinical trials through data review, cleaning, reconciliation, and query management. The role also covers database locks, UAT, and Veeva Vault documentation.
Tavsif
- Support clinical trial data review, cleaning, query management, and vendor data reconciliation
- Review clinical data listings
- Investigate and resolve data discrepancies
- Complete CRF freeze and database lock activities
- Coordinate with internal and external stakeholders
- Conduct UAT for listings, screens, and edit checks
- Maintain study documentation in Veeva Vault/eTMF
- Review and reconcile local laboratory and other external data
Talablar
- At least four years of Clinical Data Management experience in a CRO, pharmaceutical, or biotechnology setting
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or a related scientific field
- Hands-on experience with EDC systems, preferably Medidata RAVE and Oracle Clinical
- Experience with data review, query management, vendor reconciliation, and database lock activities
- Working knowledge of clinical research regulations, GCP guidelines, and clinical trial processes
- Veeva Vault and eTMF documentation experience is preferred
- Experience using clinical data review tools
- Knowledge of ICH-GCP, regulatory guidelines, and 21 CFR Part 11
- Experience with Clinical Data Workbench
- Strong written and verbal communication abilities