requirements. Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory... submissions. Support the preparation of study-related materials, such as informed consent forms and case report forms...
to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work... to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service...
. •  Performs other work-related duties as assigned. •  Minimal travel may be required. Get to know Syneos Health Over... of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make...
of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make... us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youâ...
clinical deliverables of a study Subject matter expertise in the designated therapeutic area Prior monitoring... experience is preferred Ability to travel up to 20% What ICON can offer you: Our success depends on the quality...
of clinical study teams. What You Will Be Doing: Leading the operational planning and execution of clinical trials, ensuring... and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave...
and Qualifications: Bachelor of Arts/Science or equivalent degree in Computer Science or related area of study 6+ years of SAP..., and Project System. Understanding of financial accounting and cost accounting principles. Ability to work with both business...
Position is based in Mexico City. The ideal candidate will be able to travel to Monterrey, Querétaro, Toluca, Morelia... diseases, neurological disorders, genetics) MSL in the pharmaceutical industry is required OR strong history of study...
) As a Regulatory Technician you will work with the Clinical Trials Information System (CTIS), and will also provide support... management and upload to CTIS and liaise with internal/external stakeholders to resolve Actively maintain applicable study...
clinical deliverables of a study Subject matter expertise in the designated therapeutic area Prior monitoring... experience is preferred Ability to travel up to 20% What ICON can offer you: Our success depends on the quality...