Our client, a global pharmaceutical company based in Cork, is seeking a Medical Writer to join their team.
As a medical writer, you will collaborate with cross-functional teams to facilitate the publication of scientific data and regulatory documents.
This contract role offers hybrid working arrangements.
Responsibilities
* Plan, write, edit, review, and coordinate the publication of scientific data through peer-reviewed journals and forums or regulatory documents.
* Facilitate trial development and product registration.
* Evaluate and ensure quality checks for accuracy, collate reviewer comments, adjust document content as required, and prepare final versions.
* Ensure final documents and supporting quality check documentation are stored in the appropriate document management system.
* Built relationships with vendors and alliance partners.
* Maintain and enhance knowledge of therapeutic areas, including disease states and compounds for assigned projects.
Requirements
* A PhD is preferred but candidates with a Bachelor's Degree will be considered.
* A graduate degree with a formal research component or in life sciences is required.
* Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience is essential.
* Experience in clinical trial processes or regulatory activities is preferred.
* Prior experience writing regulatory or clinical trial documents is also beneficial.
* Demonstrated mastery of written English with experience in medical, scientific, or technical writing fields (at least 1 year).
* Professional verbal skills in English are necessary.