JOB TITLE: Director, Regulatory Affairs
BENEFITS: Competitive annual salary
Ensure the team collaborate and work closely with key functional groups eg. Marketing, Sales and Quality Assurance to drive company-wide or cross-departmental initiatives.
Provide quality and timeliness of regulatory and medical input into cross-functional teams.
Manage regulatory & medical affairs budget.
Strong people management skills experience is a MUST, with at least 5 years experience managing a team.
Covered a regional market for more than 3 years. Asia region will be a huge advantage.
Develop procedures and processes to ensure organisational health and operational excellence.
Sound business acumen and market access knowledge.
10-15 years experience will be critical for the role.
Post-graduate degree in Life Sciences, Masters in Drug Development.
Familiar with clinical, regulatory, registration, reimbursement and compliance issues in Asia.
Strong organisation skills and ability to handle multi-projects.
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the global Life Sciences industry. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Sales & Marketing, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance, Supply Chain & Logistics and Bioinformatics.
If you would like to discuss this vacancy further, please call Sheila Heng, EA Registration No.: R1105454, on +65 3163 8900, or email firstname.lastname@example.org. If this role is not suitable, Sheila is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
EA Licence No.: 15S7766