Beschreibung
Job DescriptionThis position will take on project responsibilities for Medical Writing for the Clinical Trials process, covering but not limited to;
- Prepare all documentation required by internal requirements to an excellent standard, working in collaboration with other teams and stakeholders.
- Carry out all required research and data analysis necessary to create excellent and accurate Clinical documentation.
- Ensure that all documentation is accurate and compliant with internal and external regulations.
- Effectively project manage all writing related tasks.
- Build relationships with key stakeholders to assist with smooth transferal of data.
- 5+ years of professional experience as a Medical Writer for Clinical Trials.
- Systematic and precise approach to work within procedures, rules and regulations.
- Strong time and project management skills.
- Excellent communication skills in English, reading, writing and speaking.
- Post Graduate degree in a Medical related field.
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