Department: Regulatory

Schedule: Full Time

Location Note: This position may be located remotely or in Durham, North Carolina.


Chimerix Inc. is seeking a Clinical Research Scientist/Medical Writer to write or coordinate the preparation of, all clinical, regulatory, and scientific documents intended to support clinical and regulatory deliverables for Chimerix Inc. drug development project teams. The scope of the role includes authoring, review, managing document timelines and workflow, and quality assurance check of documents and coordination of external medical writers.


At Chimerix Inc., you will have opportunities to learn, develop, contribute, and be challenged... all while making a difference in the lives of our patients.


Chimerix Inc. is an Equal Opportunity/Affirmative Action Employer - EOE Minorities / Females / Protected Veterans / Individuals with Disabilities.


Chimerix Inc. is a vaccinated work environment where all employees are expected to be vaccinated against COVID-19 and provide proof of vaccination.  We will provide any accommodations as required by law.


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