Medical Writer I/II
Parexel(4 months ago)
About this role
This role at Parexel supports the development of therapies by creating clinical documentation used in drug development and regulatory submissions. It operates within a global clinical development services environment, partnering with clients and cross-functional teams to deliver regulatory-ready clinical content.
Required Skills
- Clinical Writing
- Regulatory Writing
- Clinical Study Reports
- Informed Consent
- Safety Reports
- Quality Control
- Medical Editing
- Literature Review
- ICH-GCP
- FDA Guidelines
+8 more
Qualifications
- Bachelor's Degree in Life Sciences/Health Related Sciences
About Parexel
parexel.comFor over 35 years Parexel has been a trusted global CRO and biopharmaceutical services company. Learn more about how we can help.
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