BDS

Looking for clinical Database Developer experience in eCRF build and edit checks build in Veeva studio; Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process. Providing support for the mapping and transformation of clinical data to CDISC SDTM standards. Work independently and accountable for study Data Management deliverables; Coordinate with Biostatistician, Clinical, Medical and local study team as applicable

Masters degree, diploma, life sciences, pharmacy, public health, healthcare or other related discipline with minimum 2 years of relevant clinical trial monitoring experience.

Characterization of Novel Anti-BCMA Antibody Drug Conjugate as an Immunotherapeutic Agent for Multiple Myeloma. M.Pharm, ME, M.Tech degree holders with relevant experience in the cancer research. First Class Post Graduate degree MSc in life sciences, Biochemistry, Biotechnology, Microbiology, Molecular Oncology, including the integrated PG degree with three years of experience

Provide technical support to the DteGHS, Ministry of Health & Family Welfare by implementing the priorities of the WHO-Global Patient Safety Action Plan 2020-2030 & National Patient Safety Implementation Framework. Facilitate in coordination with the Center of excellence to include Patient Safety activities in their State PIPs under the guidance of MoHFW.

Plan, operationalize, and coordinate the Health and Biomarker component of the LASI project in coordination with IIPS team. Manage the technical aspects of data validation, adherence to methodologies, and coordination with LASI head office staff. Monitoring and Evaluation Knowledge, Understanding of health monitoring and evaluation systems, including the definition and measurement of core health indicators.

First Class Post Graduate degree from a recognized University in subjects listed below OR Second Class Post Graduate with Ph.D. degree from a recognized University in subjects listed below Eligible subjects for educational qualification : MSc Nursing, Genetics, Medical Genetics, Immunology, Molecular biology, Biotechnology, Pharmacology

MBBS, BDS Or M.Pharma, MPT, M.sc Nursing, M.sc in life Sciences or Equivalent. Or Graduate in life Sciences BAMS, BHMS, B.sc Nursing, BPT or Equivalent from recognized University with three years of experience recognized Institution. 

As a Principal Medical Writer you will play a pivotal role in leading the Medical Writing efforts for Marketed Products and Lifecycle Management, both globally and at regional, local levels. You will represent the department as a subject-matter expert on clinical study teams, leading document-related meetings and reviewing study-related documents.