Principal Medical Writer
We’re looking for an experienced Principal Medical Writer to join our team at PPD-Pharmaceutical Product Development. In this role, you’ll be responsible for taking complex medical and scientific information and preparing high-quality regulatory document deliverables. You’ll need to have excellent technical writing skills, as well as the ability to effectively collaborate with other internal and external stakeholders. If you’re looking for a challenging and rewarding opportunity to put your medical writing and scientific knowledge to the test, this role could be the perfect fit for you.To be successful in this role, you must have a PhD, PharmD, or equivalent degree in a related scientific field, and at least 5 years of experience in medical writing. You should also have a strong understanding of regulatory submission processes, including the preparation of documents for regulatory submissions. We’re looking for someone with excellent attention to detail, excellent communication skills, and the ability to work independently with minimal supervision. If you think you have the right skills and experience for this role, we’d love to hear from you!
Responsibilities:
Prepare high-quality regulatory documents for submission based on complex medical and scientific information.
Collaborate effectively with internal and external stakeholders.
Utilize technical writing skills to ensure accuracy and quality of documents.
Maintain a strong understanding of regulatory submission processes.
Exercise excellent attention to detail and communication skills.
Work independently with minimal supervision.
PPD-Pharmaceutical Product Development is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
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Responsibilities:
Prepare high-quality regulatory documents for submission based on complex medical and scientific information.
Collaborate effectively with internal and external stakeholders.
Utilize technical writing skills to ensure accuracy and quality of documents.
Maintain a strong understanding of regulatory submission processes.
Exercise excellent attention to detail and communication skills.
Work independently with minimal supervision.
PPD-Pharmaceutical Product Development is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Apply tot his job
Apply To this Job