BAMS

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.

Professionals having proven competency and success in their area of specialization, with at least 10 years of post- qualification experience and should possess minimum M.Sc, B.Tech, BE, MCA, MPH, B.Pharma, BAMS, BSMS, MD in AYUSH Or equivalent qualifications in relevant subject. 

Develop study protocols, standard operating procedures, and other essential documents in line with regulatory guidelines. Oversee the implementation of study activities, ensuring adherence to timelines, quality standards, and Good Clinical Practice guidelines. 

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.

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. 

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.

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