Medical Content Writer - - Pfizer - 5 to 10
- Pfizer
- 5 - 10 years
- Remote
- 1 month ago
- Email to a friend
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Job Description
- Your strong documentation skills will be an asset for the team
- You will help us draft manuscripts on clinical studies and scientific reports for submission to regulatory agencies or in-company use
- You will also help with summaries, monographs, comprehensive reviews, scientific exhibits and projects requiring skill in medical communication
- Your planning skills will help in preparing forecasts for resource requirements, and providing areas of improvement for products, processes or services
- Through your comprehensive knowledge of principles, concepts and theories of the discipline, you will also work towards advancing new concepts and methodologies
- You will be able to take a leadership role to facilitate agreements between different teams
- It is your problem solving ability that will make Pfizer ready to achieve new milestones and help patients across the globe.
- Provide guidance, lead/co-lead projects, manage own time to meet objectives, plan resource requirements for projects across the division.
- Drive document strategies and messages in a collaborative way with relevant project team subject matter experts.
- Ensure documents are generated in accordance with agreed internal processes and standards, are submission ready, and are appropriately stored in agreed document management system.
- Verify accuracy of document content using source documents including clinical regulatory documents and data tables, figures, and listings.
- Ensure that medical writing deliverables conform to International Conference on Harmonization and other relevant regulatory guidelines.
- Lead a team of internal or external authors if multiple or complex documents are required for a particular project.
- Understand relationships and dependencies between documents and analyses produced for regulators.
- Independently perform Quality Control (QC) review and manage QC projects in accordance with agreed upon timelines.
- Contribute to the training of colleagues on quality standards and processes.
- Develop and sustain constructive relationships within other Pfizer lines including country organizations.
- Record findings and identify appropriate corrections to address findings.
- Bachelors Degree
- Demonstrated experience in document QC and/or medical writing in the pharmaceutical or biotech industry
- Experience in interacting with cross functional study team members
- Solid understanding of medical terminology and clinical trials
- Excellent interpersonal and communication skills
- Ability to plan, organize, prioritize, and execute multiple tasks within assigned objectives
- Proficiency with computer applications (MS Office)
- Masters degree
- Experience with software commonly used to present and analyze data
Job Classification
Industry: Pharmaceutical & Life SciencesFunctional Area: Pharmaceutical & Life Sciences
Role Category: Other Hospital Staff
Role: Pharmacist
Employement Type: Full time
Contact Details:
Company: PfizerLocation(s): Remote
Keyskills: QC Quality standards Pharma Clinical trials Healthcare Manager Quality Control MS Office Medical writing Document management system
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