Join Our Team and Make a Difference in Clinical Research
At MEDEX SMO, we believe that our success is driven by our talented and passionate team. We are always seeking dedicated individuals who are eager to contribute to the advancement of clinical research and make a positive impact on patients' lives. If you are looking for a rewarding career in the field of clinical trials, consider joining our team.
Why Work with Us?
- Meaningful Work: Join a dynamic and collaborative environment where you can contribute to the development of life-changing therapies. Your work will directly impact the lives of patients and help advance medical science.
- Professional Growth: MEDEX SMO is committed to investing in the professional growth and development of our team members. We provide ongoing training opportunities, mentorship programs, and a supportive work culture to help you reach your full potential.
- Cutting-Edge Research: Work with leading researchers and organizations on innovative clinical trials. Stay at the forefront of medical advancements and gain exposure to a diverse range of therapeutic areas.
- Team Collaboration: Collaboration is at the heart of our success. Join a team of talented professionals who are passionate about their work and collaborate closely to achieve exceptional results.
- Work-Life Balance: We understand the importance of maintaining a healthy work-life balance. We offer flexible work arrangements, competitive compensation packages, and comprehensive benefits to support your overall well-being.
Open Positions : MEDEX SMO is currently seeking qualified individuals for the following positions in whole Turkey in case of recruitment;
Clinical Research Coordinator
- Responsible for the coordination and management of clinical trial activities at the research site.
- Conduct participant screening, enrollment, and data collection.
- Ensure compliance with study protocols, regulatory requirements, and ethical standards.
- Provide direct patient care and support throughout the clinical trial process.
- Administer study treatments and collect samples as per protocol.
- Monitor participant safety and manage adverse events.
- Oversee the collection, validation, and analysis of clinical trial data.
- Develop and maintain electronic data capture systems.
- Ensure data integrity, quality control, and adherence to regulatory guidelines.
Regulatory Affairs Specialist
- Manage regulatory submissions, including IRB/EC approvals and study amendments.
- Ensure compliance with applicable regulations and guidelines.
- Assist with the preparation of study-related documentation.
How to Apply: To apply for a position at MEDEX SMO, please send your resume and a cover letter to email@example.com. In your cover letter, please include details about your relevant experience, qualifications, and why you are interested in joining our team. We will review your application and contact you if your qualifications match our requirements.
Join our team today and play a pivotal role in advancing clinical research and improving patient care.