Associate/Sr. Associate

88130 | 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 Coordination