BDS

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.

Sepsis- related mortality in neonates in India, A multi-disciplinary, multi-institutional research program for context -specific solutions; As an academic Clinical Research Unit, to undertake & provide end -to- end clinical study support for investigators and SMEs in study planning, set up, conduct. project management, monitoring, data management, safety reporting, analysis and report writing

Contributes, with appropriate oversight, to all relevant aspects of global clinical trial activities to deliver study outcomes within schedule, budget, quality, compliance and performance standards. May lead specific aspects of global clinical trial. High quality contributions to study documents e.g. protocol, ICF, clinical sections of CTA -Clearly demonstrates Novartis Values and Behaviors i.e. Innovation, Quality, Collaboration, Performance, Courage and Integrity.