Associate/Sr. Associate

87566 | Experienced

Digital Services

Role Description

•Any Life Science graduate with minimum 3 months experience in Clinical document management /Clinical data management/Clinical research Coordination. 
•Exposure to Medical coding / QA – QC in clinical research / Regulatory affairs/ Regulatory publishing / PV is needed. 
•Should have knowledge of ICH GCP principles and Clinical drug development process. 
•Experience working on eTMF (Electronic Trial Master File ) tool is preferred. 
•Must be comfortable working in rotational shifts. 
•Interns in clinical research and clinical data management with 3 months of exposure too can apply
 

Qualifications

  • Any Life science Graduate (B Pharm, M Pharm, BSC with Biology, Zoology, Botany, Biotechnology, Bioinformatics specialization) or any other medical graduate

Desired Skills and Competencies

  • Minimum 3 months experience in Clinical document management /Clinical data management/Clinical research Coordinatio