Highly Skilled Scientific Expert

1 day ago

Agra, Uttar Pradesh, India beBeeScientificSme Full time US$ 90,000 - US$ 1,20,000

Job Title: Scientific SME

About this role

We are seeking a highly skilled Scientific Subject Matter Expert to play a key role in developing high-quality proposals and contracts that align with study protocols and integrate scientific best practices.

This is a fantastic opportunity for an experienced professional to utilize their expertise in scientific principles, writing skills, and communication abilities to represent our organization in client meetings and industry conferences, supporting business growth and strong sponsor relationships.

Key Responsibilities
  • Develop proposals and contracts that meet the highest standards of quality and integrity.
  • Collaborate with cross-functional teams to identify opportunities and needs described in RFPs and associated documentation.
  • Communicate effectively with clients and stakeholders to ensure seamless execution of projects.
  • Manage proposal development, alignment with study protocols, and integration of scientific best practices.
  • Draft, review, and assist with change orders, revisions to proposals and contracts.
  • Optimize proposal design by identifying opportunities and needs described in RFPs and associated documentation.
  • Communicate risks associated with proposals and contracts.
  • Meet deadlines by establishing target dates and prioritizing information gathering, writing, review, and finalization.
  • Prepare quality assumption tables to align with study protocol.
  • Participate in internal and external meetings related to proposals and contracts.
  • Represent our organization at conferences and meetings with clients and prospective clients.
  • Interact with, build relationships with, and support sponsors and vendors.
Requirements
  • Bachelor's degree in English, Journalism, Marketing, Communications, Business, Computer Science/MIS, Science, Law, or related area.
  • 2+ years in scientific/medical writing, proposal development, or contract management.
  • 2+ years of experience in the pharmaceutical or a regulated industry.
  • 2+ years of iCRO experience is a must.
  • Knowledge and understanding of 21CFR Part 11, Good Clinical Practices (ICH E6 GCP), Good Documentation Practices (GDP).
Physical Requirements

The employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms and talk and hear. The employee is frequently required to sit. Specific vision abilities required by this job include close vision, color vision, ability to adjust focus.

Travel

About 5 – 10 % travel (domestic and/or international)

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