Are you a highly organized and detail-oriented individual with a passion for healthcare and technology? Do you thrive in a fast-paced and dynamic work environment? IQVIA is seeking a Site Activation Specialist to join our team and help drive the success of clinical trials. As a Site Activation Specialist, you will play a crucial role in ensuring the timely and efficient activation of study sites, with a focus on meeting regulatory and compliance requirements. We are looking for a proactive and collaborative individual with a strong understanding of the clinical trial process and excellent project management skills. If you are ready to make a difference in the world of healthcare and take on an exciting new challenge, we encourage you to apply for this role.
- Coordinate with internal teams and external stakeholders to ensure timely and efficient activation of study sites for clinical trials.
- Develop and maintain detailed project plans for site activation, including timelines and milestones.
- Ensure compliance with all relevant regulations and guidelines related to site activation.
- Conduct site feasibility assessments and provide recommendations for potential sites.
- Collaborate with study teams to identify potential risks and develop mitigation strategies.
- Communicate regularly with study sites to provide updates and gather necessary information for activation.
- Manage site contracts and budget negotiations.
- Develop and maintain relationships with key stakeholders, including site personnel and regulatory authorities.
- Monitor and track site activation metrics and provide regular updates to project teams.
- Proactively identify and address any issues or roadblocks that may impact site activation timelines.
- Ensure all site activation activities are documented and completed in accordance with company policies and procedures.
- Participate in process improvement initiatives to streamline and optimize site activation processes.
- Stay up-to-date with industry best practices and regulations related to site activation.
- Train and mentor new team members on site activation processes and procedures.
- Contribute to the overall success of clinical trials by supporting the activation of sites in a timely and efficient manner.
Excellent Communication And Organizational Skills
Bachelor's Degree In Life Sciences Or Related Field
At Least 2 Years Of Relevant Experience In Clinical Research Or Site Management
Strong Knowledge Of Fda Regulations And Ich-Gcp Guidelines
Ability To Multitask And Work Under Tight Deadlines In A Fast-Paced Environment
Communication Skills
Project Management
Vendor Management
Data Analysis
Time Management
Contract Negotiation
Attention to detail
Budget management
Regulatory compliance
Relationship
Clinical Trials
Site Selection
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
Critical thinking
Teamwork
Active Listening
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Site Activation Specialist in Seoul, South Korea is approximately $50,000 to $70,000 USD per year. This can vary depending on factors such as years of experience, specific industry, and company size. It is important to note that salaries may also be affected by the current economic climate and job market conditions.
Apply with Video Cover Letter Add a warm greeting to your application and stand out!
IQVIA, formerly Quintiles and IMS Health, Inc., is an American multinational company serving the combined industries of health information technology and clinical research.

Get interviewed today!
JobzMall is the world‘ s largest video talent marketplace.It‘s ultrafast, fun, and human.
Get Started