Job title: Medical Writer II
Company: Parexel
Job description: Why Work at Parexel
There are pivotal moments in every career: Sharing new treatments. Improving processes. Delivering life-saving advances. The people who succeed are the ones who make the journey go further and faster every time. What if you had a partner to support you as you reach the next level in your professional path? A partner who believes a collaborative environment is key to achieving your goals? A partner who is dedicated to your health and wellness so you can help make a difference in the lives of millions worldwide?
That’s Parexel. We’re a diverse team of professionals focused on one goal: getting treatments into the hands of those who need them most. Working together, the results we bring to our clients and the opportunities we bring to our team get better with every step.
How can we help you on your journey? Find your path, and learn more on , , , , and .
Qualifications
- Demonstrated understanding of clinical research, the drug development process, and industry
guidelines and regulations, e.g., ICH-GCP.
- Extensive clinical/scientific writing skills.
- Scientific background essential; writing experience includes multiple clinical study reports.
- Advanced word processing skills, including MS Office (expertise in Word); software and systems
knowledge or ability to learn and adapt to various IT systems: document management systems,
collaborative authoring (e.g., SharePoint), and file conversion and databases (Excel).
- Fluent in written and spoken English with appropriate attention to phraseology, grammar, and
punctuation.
- If required to perform translation work and quality control of documents written in non-English
language, proficiency in relevant language is a prerequisite.
Education:
- Bachelor’s degree in Life Sciences/Health Related Sciences or equivalent.
Job Description
e Medical Writer II will research, create, edit, and
coordinate the production of clinical documents associated with submissions to regulatory authorities,
including but not limited to: study protocols, model informed consents, interim and final clinical study reports,
and safety update reports. The Medical Writer II will also be responsible for the production of clinical study
documentation associated with clinical trials that may not be included in a regulatory submission. The
Medical Writer II may serve as the primary client contact.
Job Family
Medical Writing
Expected salary:
Location: India
Job date: Sun, 20 Feb 2022 06:17:38 GMT
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