- Prepare and finalize clinical documents such as, but not limited to, protocols/amendments, study reports, summary documents, regulatory responses, and briefing documents.
- Participate in cross-functional document planning and review meetings. Interact with peer and external writers, as well as colleagues from other departments. Able to lead document-level writing teams with supervision.
- Establish document timelines and strategies in accordance with internal processes, with mentorship from functional management and the clinical team, as needed.
- If a lead writer for a document: Be the primary point of contact and champion for medical writing activities. Responsible for planning and leading writing activities for assigned documents.
- Acquire, maintain and apply knowledge of the industry, company, and regulatory guidelines.
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Medical Writing Scientist - High Wycombe, United Kingdom - Johnson & Johnson
Description
Medical Writing Scientist
We are recruiting for a Medical Writing Scientist to join the Medical Writing team to support our Medical Affairs portfolio across therapeutic areas. The position may be located in the United Kingdom [this is a global role and is open to other locations]. Remote work options may be considered on a case-by-case basis, if approved by the company.
At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing, and preventing some of the most devastating diseases of our time. Janssen Research & Development discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, pulmonary hypertension, and cardiovascular and metabolic diseases.
Are you ready to join our team? Then please read further
Key Responsibilities:
Depending on the experience and level of the appointed position, your responsibilities will cover a range of activities including:
