Clinical Trial Assistant - Αθήνα

The Clinical Trial Assistant role involves supporting clinical studies, maintaining trial documentation, and ensuring ethical compliance. · ...

+Job summary · Redefine Clinical Operations at Excelya by joining our team as a Clinical Trial Assistant. · +Prepare study related documents for Site Regulatory Package approval. · Collect initial package of essential documents required for drug shipment. · ...

We are seeking a Clinical Trial Assistant to provide clinical and scientific expertise required for the successful completion of Excelya's projects. · Prepare, collect and upload all study related required documents to (e)TMF to gain Site Regulatory Package approval prior to Site ...

We are seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials. · Assist in the coordination and administration of clinical tr ...

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. · We will contribute to the success of clinical trials by ensuring data integrity, · participant safety,and compliance throughout the study lifecycle.Advanced degree in a rel ...

We are currently seeking a Clinical Research Associate (CRA) to join our diverse and dynamic team. · Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. · ...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners. · ...

Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors studies or multi-protocol programs as determined by the Sponsor's requirements. · Bachelor's degree in related field · 3 years' experience and/or ...

Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor's requirements. · ...

+Job summary · ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence. · +QualificationsAdvanced degree in a relevant field such as life sciences, nursing, or medicin ...

The Associate Central Monitor is supporting the completeness, quality and integrity of the subject data in the clinical trial database under Risk Based Monitoring (RBM) mode. · Assist to set up and test study level Risk-based Monitoring system.Bachelor's degree or above of equiva ...

The Field Medical Advisor acts as the first point of contact for any medical activity related to her/his product/ area of responsibility. · Provide scientific information and support: · ...

Veeda Lifesciences is seeking a Medical Coder based in Athens, Greece for its growing international hematology/oncology Clinical Trials program. · Receive listings from Data Management team to perform coding (using MedDRA and WHO DRUG dictionary) accurately and efficiently. · ...

+ Medical Monitors provide medical input to global clinical studies and advise teams and business partners while focusing on patients' safety and well-being.+ Serve as medical point of contact for internal project team study sites and study sponsor for medical matters related to ...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while focusing on patients' safety and well-being. · ...

We are seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team.As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requiremen ...

+We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry. · ...

We are seeking a Senior Clinical Research Associate (CRA) to join our team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities. · Monitoring clinical trial sites. · Conducting site visits. · ...

PSI medical monitors provide medical input to global clinical studies and advise the teams and business partners. · ...

As an Accountant you will be at the forefront of managing critical financial transactions ensuring accuracy compliance and effective financial planning. · ...