Study Startup Specialist II

Take your career to the next level and lead challenging study activation process on a country level. You will support clinical research teams and ensure PSI projects start smoothly and on time. You will: Collaborate with the project team for site activation processes Assist in feasibility research and site identification Facilitate site agreement and budget negotiations Collect site documents for IRB/IEC submission and/or IP-RED process Coordinate translation and review of study-specific documents Identify and escalate project-specific issues as needed Prepare and submit the study dossiers to sites, competent authorities, IRBs/IECs Prepare IP-REDs packages Support initial distribution of Investigational Product(s) and clinical study supplies to sites Ensure exchange of information and documentation with investigational sites, off site facilities and vendors Participate in development of site-specific startup timelines and enrolment projections and is responsible for meeting the site activation targets Train and coach department staff on startup processes College/University degree in Life Sciences or an equivalent combination of education, training and experience At least 2 years of full-scope Study Startup experience in the country/region Full working proficiency in English Well-developed communication and organizational skills Ability to negotiate and build relationships at all levels We offer: Excellent working conditions Extensive training and friendly team Competitive salary and benefits package Opportunities for personal and professional growth Two days working from home following successful completion of probation Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.