Position: Senior Medical Writer
Role Overview:
As a Senior Medical Writer at Parexel, you will utilize your extensive scientific knowledge and writing skills to effectively communicate complex clinical research data to various stakeholders, including regulatory agencies, medical professionals, and the public. This role involves collaborating with cross-functional teams to develop a range of clinical research documents, such as informed consent forms, clinical study reports, pharmacovigilance documents, and more. You will also drive process improvements, provide technical mentoring, and support the Medical Writing Services management with client interactions and proposal development.
Key Responsibilities:
Document Management:
Clinical Study Report Narratives:
Signal Detection and Management:
General Responsibilities:
Qualifications:
Experience:
Education:
Skills:
Personal Traits:
Why Join Us?
At Parexel, we are committed to fostering a culture of inclusivity and collaboration. We provide continuous learning opportunities through mentoring, job shadowing, job rotation, and leadership roles. Your career development and advancement are guided by global standards and your personal development plan. Join us to make a meaningful impact on patients' lives and grow within a supportive and dynamic environment.
Ready to Apply?
If you have the skills and experience to excel in this role and are passionate about advancing clinical research, we encourage you to apply and become a key part of our team at Parexel.
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