- Location
- Seoul, Republic of Korea, Korea, Republic of
- Type
- Full-time
- Department
- Healthcare
- Seniority
- Manager
- Experience
- 8+ years
- Source
- Workday
Description
Deliverables:
- Provide local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries.
- Operational oversight of assigned projects at the country level for end-to-end project management from start-up through to closeout activities.
- Ensure the local trial team is delivering high-quality data and trial documents/records that are compliant with the assigned clinical trial protocol, company Standard Operating Procedures (SOPs), International Conference on Harmonization for Good Clinical Practice (ICH-GCP), and regulatory requirements.
- Partner with the Clinical Program Leader (CPL), Global Clinical Trial Support, and Global Trial Leader to ensure overall study delivery at the country level.
Education and Experience Requirements:
- BA/BS degree in a health or science related field.
- This role acts as a local project manager in a dedicated team, focusing on Real World Evidence (late-phase research).
- Minimum 8 years of pharmaceutical or CRO industry experience in a global environment, including a minimum of 2 years as a Clinical Project Manager.
- Experience in Real World Evidence with PMS(RMP), Phase IV, and Observational studies is highly required.
- Excellent communication skills including good written and spoken English; and Flexible, accountable and comfortable in working in a global and regional environment.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
