Qualifications & Skills
- Basic understanding of scientific and medical concepts
- Basic understanding of drug development
- Basic knowledge of GCP and ICH regulations98
- Ability to work as part of a cross-functional team
- Ability to identify and escalate problems and contribute to issue resolution
- Time management and organizational skills
- Strong communication skills with advanced oral and written English skills
- Advanced computer, database skills
- Independent, strong analytical, and problem-solving skills
- Able to work under pressure, with a strong sense of responsibility and accountability.
Requirements:
- M.D. with minimum 1 year of clinical work experience in a patient care setting or 2 years relevant pharmaceutical, drug development, and/or drug safety experience.
Education Requirement:
M.D./D.O. or equivalent degree in Medicine
English: Advance (C1 Level)
Work Experience:
Minimum 1 year of Experience in a patient care setting, or 2 years relevant pharmaceutical, drug development,
and/or drug safety experience.
- Please submit your CV in English
Required Skills:
Adaptability, Adverse Event Report, Clinical Trial Management, Data Integrity, Data Management, Detail-Oriented, Drug Safety Surveillance, Good Clinical Practice (GCP), Medical Device Management, Protocol Development, Regulatory Communications, Regulatory Compliance Audits, Regulatory Interpretation, Regulatory Reporting, Training and Development