We are seeking a highly skilled Medical Writer Consultant to join our team at ICON plc, a world-leading healthcare intelligence and clinical research organization.
Job Description:
* Conducts technical project management, including scope of work development, contract initiation, and project milestones, timelines, deliverables, and budgets
* Supports project lead/director on other projects as needed
* Identifies risks with completing specific deliverables and effectively executes strategies to minimize them
* Maintains understanding of project requirements and identifies scope creep as it happens
* Communicates efficiently and effectively across the ICON project team
* Establishes and maintains regular meetings with clients, including drafting agendas, managing calendars, summarizing notes, and tracking agreed actions
As a Medical Writer Consultant, you will have excellent communication and interpersonal skills, with the ability to effectively collaborate with multidisciplinary teams and stakeholders. You will have experience working in Market Access in the pharmaceutical industry (pharma company or consultancy) and possess direct HTA/HE experience and understanding. A Bachelor's degree or equivalent is required.
Key Responsibilities:
* Assists in document and information revisions and updates for different types of evidence dossiers
* Develops approach to assigned piece(s) of the client project
* Conducts appropriate searches of literature or guidance documents with limited direction of senior staff
* Assesses project relevant data, identifies issues, and prepares gap assessments
Behaviours:
* Proactively and independently expands knowledge base and remains current on developments, trends, and best practices for subject matter expertise
* Efficiently manages own workload with respect to project scope, timelines, and quality
* Maintains strong understanding of the pharma/biotech/medical device industry landscape as it relates to technically relevant trends and challenges
Medical Writers can specialize in areas such as regulatory affairs, pharmacovigilance, or medical communications.