Job Details
Posted 15 February, 2026
Job Id: 625572
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Clinical Site Coordinator
Job Description
Join Our Team as a Clinical Site Coordinator – Drive Innovation in Clinical Research
Are you passionate about advancing medical science and making a tangible difference in patients’ lives? We are seeking a dedicated Clinical Site Coordinator to play a vital role at our site in Astana, Kazakhstan. This full-time position offers a unique opportunity to work on groundbreaking clinical studies, supporting our mission to connect patients, physicians, and sponsors seamlessly and efficiently.
In this role, you will act as a key liaison between the medical site and sponsors or CROs, ensuring smooth study operations from patient enrollment to regulatory compliance. Your efforts will directly impact the success of clinical trials, helping to accelerate the development of revolutionary treatments that can change lives.
Required Skills:
- Minimum 2 years of experience as a Clinical Site Coordinator or in a similar role within clinical research
- Comprehensive understanding of ICH-GCP guidelines and clinical trial protocols
- Strong organizational skills with the ability to manage multiple tasks efficiently
- Excellent communication skills in both English and Kazakh
- Proven ability to work effectively under pressure and meet tight deadlines
- Attention to detail and accuracy in data entry and documentation
- Ability to handle regulatory documents and support study audits or inspections
Nice to Have Skills:
- Experience with electronic data capture (EDC) systems
- Familiarity with clinical trial contracts, budgets, and site payments
- Prior exposure to regulatory reporting, including adverse events and protocol deviations
- Flexibility to adjust working hours based on study needs
Preferred Education and Experience:
- Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or Laboratory Analytics
- At least 2 years of hands-on experience working at clinical research sites or in clinical trial coordination
Other Requirements:
- Willingness to work in a dynamic environment with fluctuating schedules
- Ability to travel locally for site visits or monitoring activities if needed
- Commitment to maintaining the highest standards of study conduct and compliance
Take this opportunity to contribute to cutting-edge clinical research that has the potential to transform healthcare. If you’re ready to join a forward-thinking organization dedicated to quality and innovation, apply now to become part of our dedicated team as a Clinical Site Coordinator.
Equal Opportunity Employer
We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
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