Imaging Innovation Leader

7 days ago

Madurai, Tamil Nadu, India beBeeScientific Full time US$ 1,20,000 - US$ 1,50,000

Transforming Imaging for a Cure. At our company, we push the boundaries of imaging science, technology, and services to bring curative innovations to humanity. Our team is driven by a passion for our mission to tailor each clinical trial's imaging to maximize the potential to demonstrate efficacy.

We are seeking a Subject Matter Expert (SME) to join our Business Development Operations team. This role will focus on crafting high-quality proposals and contracts, aligning them with study protocols, and integrating best practices in scientific research. The SME will also represent us in client meetings and industry conferences, supporting business growth and fostering strong sponsor relationships.

Responsibilities
  • Manage the coordination and development of business proposals (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.
  • Identify and communicate risks associated with proposals and contracts.
  • Meet proposal and change order deadlines by establishing target dates and identifying 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.
  • Represent us in conferences and meetings with clients and prospective clients.
  • Present at conferences and other industry meetings.
  • Interact with, build relationships with, and support sponsors and vendors.
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).

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