BDS

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.

To establish a ready network of clinical trial units across the National Cancer Grid to promote multi-centric collaborative research in the field of drug and device development funded by Biotechnology Industry Assistance Council. MBBS, BDS, MSc Biostatistics , MSc Clinical Research, MSc Nursing, Any postgraduate degree in life sciences with PG Diploma or training in clinical research.

BDS, BAMS, BHMS, B.Pharm, BSc, Any Degree. Three years experience of working in a 500 Bedded Hospital. Master in Health, Hospital Administration, PG Diploma in Health Hospital Administration.

B. Pharma, D. Pharma, BHMS, BAMS, BUMS, BDS, B.Sc. Life science, M.Sc. Life Science, and Diploma in Clinical Research. Preference will be given to the candidates having relevant experience in Clinical Research.

As a Senior Specialist, Expert Medical writer , you will support the Medical Writing efforts for Marketed Products and Lifecycle Management, both globally and at regional/local levels. Independently prepares of clinical and regulatory documents such as Protocols, Clinical Study Reports, or Investigator Brochures.

Contribute to the development and implementation of new safety-related systems, processes, and procedures within the process. Support a performance-driven culture.