Medical Writer

3 days ago


India Excelya Full time

Excelya is one of the leading CROs in Europe, founded in 2014 and headquartered in Paris. Our global team is composed of 900+ experts who understand the critical needs of clients and provide trial solutions across a broad spectrum of therapeutic areas.


We take an one-team approach to work: our shared success is the result of collaboration at every stage of a project, from regulatory affairs and clinical operations to quality assurance and strategic development.


Excelya's vision is to achieve new advances in the field of healthcare and expertise in research development. Our goal is to help our clients deliver life-changing therapies collaboratively, so we can transform tomorrow together and to become the clinical research leader in Europe.


For our team members, excelling with care means benefitting from a stimulating professional environment that encourages personal, intellectual, and operational participation so that together we can be the best in our field. We commit to giving each Excelyate the means to express their natural talents, develop their full potential and invest their unique selves in our unique projects.


To learn more about us, visit www.excelya.com.


Excelya is currently seeking a Medical Writer, experienced in redacting protocols compulsory (under EUCTR and US Final Rules). The position is full remote and can work from everywhere in India.


General Responsibilities/Tasks:

  • Lead and execute document redactions for compliance with global regulatory requirements, including EU, US, and Japan.
  • Collaborate with cross-functional teams to ensure timely delivery of redacted documents for regulatory and public disclosure purposes.
  • Review and implement best practices in document redaction to meet legal and ethical standards.
  • Provide training and mentorship to junior team members as needed.


Education and Experience

  • 2+ years of experience in document redactions within clinical research or related fields.
  • Familiarity with regulatory requirements for protocol redactions.
  • Experience with tools/software used in document redactions is preferred.
  • Background in medical writing or public disclosure activities.
  • Strong people management skills to guide and support team members effectively.


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