Senior Scientific Specialist

1 week ago

Kolkata, West Bengal, India beBeeScientific Full time US$ 90,000 - US$ 1,20,000
Job Summary

We are seeking a Scientific Expert to join our Business Development Operations team. This role will focus on developing high-quality proposals and contracts, aligning them with study protocols, and integrating scientific best practices.

Main Responsibilities
  • Manage the coordination and development of business proposals (request for proposal/request for information: RFP/RFI) and contracts for prospects and clients.
  • Draft, review and assist with change orders, and revisions to those documents in accordance with timelines required.
  • Optimize proposal design by identifying and clarifying opportunities and needs described in RFPs and associated documentation, specifically study protocol. Integrate experience, key differentiators, and other industry best practices into proposals and presentations.
  • Identify and communicate risks associated with proposals and contracts.
  • Meet proposal and change order deadlines by establishing target dates and identify priorities involved in information gathering, writing, review, and finalization.
  • Ensure the preparation of quality assumption tables (ATs) to align with study protocol.
  • Participate in or lead key internal and external meetings related to proposals and contracts as applicable.
  • Conduct verbal and/or written follow-up after the submission of proposals as needed. Communicate to the IE team the outcome of the negotiations/proposals focusing on conveying the expectations for each group, i.e., critical timeframes and scope of work.
  • Represent Imaging Endpoints in conferences and meetings with clients and prospective clients to present IE's capabilities, assist with proposal development, bid defenses, work order development, change order development and other business development activities as required.
Requirements
  • 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 a must.
  • Bachelor's degree in English, Journalism, Marketing, Communications, Business, Computer Science/MIS, Science, Law, or related area.
  • Knowledge and understanding of 21CFR Part 11, Good Clinical Practices (ICH E6 GCP), Good Documentation Practices (GDP).
About the Role

This is an excellent opportunity to showcase your expertise and contribute to the success of our team. If you have a strong background in scientific/medical writing, proposal development, or contract management, we encourage you to apply.

What We Offer

We offer a dynamic and supportive work environment, competitive compensation packages, and opportunities for professional growth and development.

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