Clinical Trial Documentation Life Sciences | 6 to 9 years | Gurugram

Job Description

  • Should have work experience in Clinical Trial Documentation in Consulting firms Life Sciences organizations 
  • Client consulting, Individual pursuits proposals content creation and presentation 
  • Coordination with global teams to develop solutions offers and supporting them in their local pursuits project deliveries Client project management
  • End to end management and oversight of records in Trial Master File TMF paper or electronic 
  • Supporting preparation of documentation required for regulatory inspections and audits and subsequent responses from the findings 
  • Process establishment and on going improvement 
  • Subject matter expert for trial related documentation requirements across geographies United States European Union Britain India Australia etc 
  • Coordination with and supporting all concerned departments of client and parent organization as applicable with respect to the required regulatory purpose Background
  • End to end technical and functional process 
  • Strategy and tracking  
  • Design optimization and implementation of business processes

Primary Skills

  • Clinical Trial Documentation Life Sciences

Secondary Skills

  • Ability to structure analyze and present complex ideas to business leaders and clients 
  • Strong skills in stakeholder management communication and resolving conflict 



Posted on:

September 2, 2021

Experience level:


Contract type: