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Senior Medical Writer
1 month ago
Job Overview:
The Senior Medical Writer at Caidya is responsible for preparing and delivering clinical and regulatory documents for a wide range of therapeutic areas. This role involves working independently to perform tasks such as writing, editing, formatting, compiling, and reviewing assigned documents.
Key Responsibilities:
- Develop and maintain high-quality clinical and regulatory documents, including clinical study reports, protocols, and amendments.
- Collaborate with cross-functional teams to ensure timely delivery of documents and meet project deadlines.
- Manage and maintain project timelines, ensuring that all tasks are completed on schedule.
- Provide support to other medical writers and quality reviewers to ensure delivery of documents according to timelines and within budget and to acceptable quality standards.
- Participate in client meetings and other project-related meetings and teleconferences as needed.
Requirements:
- Education: A university degree in the field of Life Sciences, Medicine, or a related field; a graduate or postgraduate degree is highly preferred.
- Experience: At least 5 years of relevant medical and regulatory writing experience in the pharmaceutical industry, with a proven track record of preparing clinical and regulatory documents with minimal supervision.
- Skills: Strong written and verbal communication skills in English, proficiency in medical terminology, and the ability to manage large and complex medical and regulatory writing projects.
Working at Caidya:
Caidya is a dynamic and innovative company that values its employees and provides opportunities for growth and development. We are committed to delivering high-quality products and services to our clients and are looking for talented individuals to join our team.
