Senior Medical Writer
Thermo Fisher Scientific
full-time
Posted on:
Location Type: Remote
Location: China
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Job Level
About the role
- Serve as primary author who writes and provides input on routine documents such as clinical study reports and study protocols, and summarizes data from clinical studies.
- May research, write or edit complex clinical and scientific and program level documents, including IBs, INDs, and MAAs.
- Review routine documents prepared by junior team members.
- Ensure compliance with quality processes and requirements for assigned documents.
- May assist in program management activities. Duties could include developing timelines, budgets, forecasts and contract modifications.
- Represent the department at project launch meetings, review meetings, and project team meetings.
Requirements
- Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years)
- Experience working in the pharmaceutical/CRO industry preferred
- Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical study reportsstudy protocolsclinical documentsscientific documentsIBsINDsMAAsprogram managementtimelinesbudgets
Soft skills
writingeditingcomplianceteam collaborationcommunication
Certifications
Bachelor's degreeAMWAEMWARAC