Responsibilities:
- Prepare technical documents to support both domestic and international regulatory submissions.
- Incorporates text graphs charts tables and statistical analysis. Proofreads circulates edits assembles inspects and duplicates product submissions. 5 years exp.
- Innovative writing with extensive knowledge and understanding of clinical research.
- Able to succinctly summarize complex scientific publications and translate science to a lay audience.
- Excellent verbal and written communication skills in addition to good interpersonal skills (i.e. build relationships with crossfunctional colleagues.
- Proficient in the use of Office 365 software such as PPT Word Excel etc.
- Proficient in the use of graphics software including Adobe Illustrator for Medical Writer II.
- Preferred for Medical Writer III but not required.
- Accurate in work efficient and contributes to process improvement.
Requirements:
- PhD in Sciences or Technology PharmD or MD for Medical Writer III with 5 years of experience in medical or scientific writing.
- Have evidence of publications in peerreviewed journals as first author and/or has written AMCP dossiers.
- Writers with prior experience in AMCP Format and AMCP Dossiers. Certification in oncology.
- Individual contributor with cross functional collaboration.
Additional Information :
All your information will be kept confidential according to EEO guidelines.
Remote Work :
No
Employment Type :
Contract