India

Clinical Trial Project Manager Associate leads the cross-functional study team in the development and execution of clinical trials and is accountable both regionally and globally to deliver trials with quality, on time, and within scope and budget. Leverage scientific and regulatory knowledge to prepare and/or provide technical consultation for clinical and regulatory documents, prepare for meetings with regulatory agencies

The purpose of the call is to support research and innovation projects that are highly relevant for scientific solution for biomanufacturing, biotechnology for improved agricultural productivity and climate resilience, RNA vaccines and biotherapeutics. The call seeks to fund applications for conducting research with a high societal relevance, both basic and applied, and innovation promoting the transition, nationally in India and Australia, as well as internationally. The priority areas of research for Round sixteen of the Indo

Sets up product development and registration objectives in aligment with RA Sub-Region Head, RA MOW Head New Product Planning, Regional Commercial team objectives and in close partnership with the local LT. Master in Life Sciences degree. PhD or Higher Degree or equivalent experience desirable

Maintain information flow at the interfaces to internal parties like packaging materials management, transport management, quality department, procurement, serialization and AW. Manage the end to end execution cycle of a Purchase Order.

Responsible for all commercial responsibilities sales targets & negotiation activities with non-clinical stakeholders. Shape & Create business strategies in line with local and regional strategies to grow Ethicon business in a given territory, with compliance and respecting profitability objectives.

Support Formulation R&D in arranging the materials for development, optimization, confirmatory and exhibit batches which are under development in Hyderabad surround locations. API samples, Impurities, Working standards support for Formulation development stage.

IIHMR University, Jaipur, is organizing the Pradanya 2025 : Global Health Management Research Conference GHMRC 2025 on February 14-15, 2025, at our campus in Jaipur, India.

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.

Author Safety Data Sheets for multiple geographies across the globe as per applicable hazard communication regulations. Derive hazard classifications for substances and mixtures using various classification regulations including but not limited to GHS, CLP, and OSHA Hazard Communication Standard.