Regional Medical Advisor

Role & Responsibilities
Plan, coordinate and oversee Phase III & IV human clinical trials
Support implementation of clinical protocols and completion of final study reports
Recruit clinical investigators and negotiate study design and budgets
Coordinate investigator site initiations and multi-center studies
Monitor protocol adherence and determine study completion
Coordinate regulatory submissions and reporting to health authorities
Participate in adverse event reporting and safety monitoring activities
Collect, analyze and manage clinical research data
Act as liaison with partner organizations under licensing or collaboration agreements
Support clinical research planning and execution activities

Qualification
Associate Degree (or higher) in Life Sciences, Pharmacy, Nursing, Clinical Research or related discipline

Experience
Minimum 1 year of experience in Clinical Research / Medical Affairs / Clinical Trials

Skills
Clinical trial coordination
Protocol compliance & monitoring
Regulatory documentation and reporting
Safety reporting knowledge
Data collection & documentation
Stakeholder coordination
Basic project management skills

About the Company
A leading global healthcare organization engaged in advanced clinical research, medical affairs and post-marketing clinical development to support safe and effective therapeutic innovations.