Associate Director Medical Writing
A company is looking for an Associate Director, Medical Writing to oversee medical writing activities for clinical development programs.
Key Responsibilities : Lead writing strategy and ensure timely delivery of high-quality regulatory documentsManage deliverables and preparation of documents for submission to regulatory agenciesRepresent Medical Writing on cross-functional teams and serve as lead writer for key regulatory submissionsRequired Qualifications : Advanced degree in a relevant scientific / clinical / regulatory field preferred;
Bachelor's degree requiredAt least 10 years of experience writing clinical / regulatory documents in the pharmaceutical or biotechnology industryExperience as lead writer for major US and / or international regulatory submissionsDemonstrated ability to manage writing activities and resources across projectsWorking knowledge of current global regulatory requirements and guidelines applicable to clinical research
Associate Medical Director Needed on the Central Coast of California
We help negotiate your salary and contract.We coordinate interviews and help with licenses.Specialized recruiters match your career preferences.Experienced support teams take care of every detail....
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