Join our team of experts in regulatory and ethics submissions of clinical studies. You will focus on facilitating the start of research projects of novel medicinal products while taking a step further in your professional career.
Officebased in Bangkok
Your role:
- Prepare clinical trial submission dossiers for Regulatory and Ethics Authorities including Import and Export license applications
- Communicate with regulatory authorities ethics committees project teams and vendors on regulatoryrelated matters
- Review translations of essential documents subject to clinical trial submission
- Track the regulatory project documentation flow
- Review documents to greenlight IP release to sites
- Manage safety reporting to authorities
- Deliver regulatory training to project teams
- Assist with feasibility research and business development requests
Qualifications :
- College/University degree or an equivalent combination of education training and experience
- At least 3 to 5 years of prior experience with clinical trial submissions in Thailand
- Full working proficiency in English and Thai
- Proficiency in MS Office applications
- Detailoriented
- Ability to learn plan and work in a dynamic team environment
- Communication collaboration and problemsolving skills
Additional Information :
We offer:
- Excellent flexible working conditions
- Extensive training and supportive team
- Competitive salary and benefits package
Take your career to a whole new level. Join a company committed to prioritizing its employees and dedicated to investing in their ongoing professional growth and success.
Remote Work :
No
Employment Type :
Fulltime