Country Approval Specialist - FSP

Job description

Join us as a Country Approval Specialist and play a pivotal role in managing and coordinating local regulatory submissions for clinical trials. You will prepare, review, and coordinate submissions in line with global strategies, supporting project-specific activities. Ideal for candidates with relevant experience and strong communication skills. Work Schedule. Standard (Mon-Fri). Environmental Conditions. Office. Job Description. Join Us as a Country Approval Specialist – Make an Impact at the Forefront of Innovation. We have successfully ... Work Schedule. Standard (Mon-Fri). Environmental Conditions. Office. Job Description. Join Us as a Country Approval Specialist – Make an Impact at the Forefront of Innovation. We have successfully sup... regulatory submissions, ethics committee submissions, regulatory strategy, patient information sheet development, informed consent form

development, regulatory compliance review, clinical trial site activation, trial status tracking, sop compliance, grant budget negotiation, feasibility coordination, medical terminology, regulatory guidelines knowledge, project coordination, negotiation, english language proficiency, teamwork, independent work, organizational skills, planning skills