Worldwide Clinical Trials in Alicante is seeking a Medical Writer to manage and lead the writing team on Phase I-IV study documents, including protocols, informed consent forms, and clinical trial reports. The ideal candidate will have a university degree in life sciences, at least 4 years of experience in medical writing, and excellent English skills. Responsibilities include document management in compliance with regulatory requirements and serving as publishing point-of-contact for necessary documents.
This role offers a dynamic environment, opportunities for ongoing training, and a commitment to diversity and inclusion.
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