Proposals Writer Ii

ICON plc

Multiple Locations
Craft clear, compelling, and client-ready proposals
Gathering and translating technical information
Balancing multiple ongoing projects
You will work at the intersection of clinical trial science, business communication, and project management to collaborate with teams of therapeutic and operational experts and executives

Job Summary

  • You will work at the intersection of clinical trial science, business communication, and project management to collaborate with teams of therapeutic and operational experts and executives.
  • As a Proposal Writer, you are a key member of the Proposals team, working with therapeutic and operational experts to develop the core strategy for trial success across all clinical phases of drug development.
  • ICON offers a comprehensive and competitive total reward package, including excellent base pay, variable pay, recognition programs, and best-in-class employee benefits tailored to support you and your family.

Matching Summary

You will work at the intersection of clinical trial science, business communication, and project management to collaborate with teams of therapeutic and operational experts and executives.

Skills & Requirements

Must-have

  • Craft clear, compelling, and client-ready proposals
  • Gathering and translating technical information
  • Balancing multiple ongoing projects
  • Attention to detail and meeting deadlines
  • Liaise with experts and facilitate communication

Nice-to-have

  • Interest in science and conveying complex concepts
  • Strategic thinker
  • Competitive, driven nature
  • Sharpen business acumen
  • Supportive team environment

Key Requirements

  • 2-3 years of professional writing experience
  • Undergraduate degree or international equivalent
  • Demonstrated writing skills
  • Applied analytical skills and strong organizational abilities
  • Strong editing skills
  • Ability to manage relationships with internal customers
  • Must be able to work under deadline pressure
  • Knowledge of CRO/pharmaceutical industry or science background preferred
  • Ability to coordinate multiple projects
  • Experience using computerized information systems and standard application software
  • Proficiency in a word processing environment required
  • Must read, write, and speak fluent English

Work Rights

Must be legally authorized to work in the UK or Ireland

Tailored Resume

Cover Letter