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Thermo Fisher Scientific is a global organization serving customers across the Life Sciences, healthcare, diagnostics, laboratory, pharmaceutical, and research sectors. The company brings together scientific technologies, laboratory solutions, clinical research services, and pharmaceutical support capabilities to help customers advance research, improve productivity, and contribute to better health outcomes. Its global portfolio includes well-known brands and services spanning areas such as scientific instruments, laboratory products, clinical research, diagnostics, pharmaceutical development, and manufacturing services. 🎯 COMPANY MISSION The company's broader mission is focused on helping its customers make the world healthier, cleaner, and safer by supporting scientific discovery, healthcare innovation, and the development of life-changing therapies.

The Central CRA will support clinical and registry studies from different stages of the study lifecycle. The role combines site management, monitoring, study start-up, regulatory coordination, documentation, and collaboration with global clinical teams. The successful candidate will work closely with investigators, site personnel, vendors, data management teams, and other stakeholders to help ensure that study activities are conducted according to approved protocols, quality standards, and applicable regulations. This is a role that requires both strong clinical research knowledge and excellent stakeholder management skills.

CtrialPro is looking for motivated candidates to join as Clinical Research Coordinators and support the smooth execution of clinical studies. The selected candidates will work with investigators, patients, sponsors, CRO teams, CRAs, and ethics committees while following study protocols and applicable clinical research standards. The position offers practical exposure to patient coordination, clinical documentation, data entry, regulatory submissions, monitoring activities, and study management. Fresh graduates with a strong interest in clinical research are encouraged to apply. This role can provide a solid foundation for future careers in Clinical Operations, Clinical Data Management, Pharmacovigilance, Regulatory Affairs, and Clinical Trial Monitoring.