Experienced Regulatory Submissions Coordinator
M
MedpaceClinical research
Remote ... in South AfricaFull-TimeJunior
Salary not disclosed
Apply NowOpens the employer's application page
Job Details
- Languages
- Very good knowledge of English.
- Experience
- At least one year of experience
- Required Skills
- Microsoft Office
Requirements
- Hold a bachelor's degree, preferably in life sciences.
- Have at least one year of experience.
- Demonstrate excellent organization and communication skills.
- Have knowledge of Microsoft Office.
- Have hands-on experience preparing, reviewing, and submitting regulatory documentation.
- Have very good knowledge of English.
Responsibilities
- Prepare, review, and file clinical trial applications to domestic and international regulatory agencies.
- Communicate with research sites in South Africa.
- Ensure submissions comply with applicable regulations and guidance documents.
- Advise sponsors on changing regulations and compliance requirements.
- Track submissions and ensure timely filing of documents.
- Provide support for feasibility.
View Full Description & ApplyYou'll be redirected to the employer's site
