About the role
- Authoring and quality assurance of project activities
- Executing project specific activities with high quality and in defined timelines
- Marking/QC/Review and/or editing of regulatory submission documents
- Performing quality control checks of documents
- Completing internal and client-specific training
- Mentoring and training of team members
Requirements
- 4-8 years’ experience in medical writing
- Well versed with regulatory requirements
- Quality review and client communication skills
- Experience in preparing clinical disclosure documents
- Understanding of clinical trial disclosure fundamentals
- Good understanding of clinical development processes
- Clear written and verbal communication skills
- Proficient in MS Word, PowerPoint, and Excel
- Career development and progression
- Supportive and engaged line management
- Technical and therapeutic area training
- Peer recognition and total rewards program
- Total Self culture providing an inclusive environment
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
medical writingregulatory requirementsquality reviewclinical disclosure documentsclinical trial disclosure fundamentalsclinical development processes
Soft skills
client communication skillsclear written communicationclear verbal communicationmentoringtraining