Job Description 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 Facilitate site agreement, contract negotiations 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 Prepareand submitthe study dossiers to sites, competent authorities, IRBs/IECs PrepareIP-REDs packages Supportinitial distribution of Investigational Product(s) and clinical study supplies to sites Ensureexchange of information and documentation with investigational sites,



off site facilities and vendors Participatein development of site-specific startup timelines and enrolment projections and is responsible for meeting the site activation targets Qualifications College/University degree in Life Sciences or an equivalent combination of education, training and experience At least 2years of full-scope Study Startup experience.

Full qualified working proficiency in English and French.

Well-developed communication and organizational skills Ability to negotiate and build relationships at all levels Additional Information We offer: Excellent working conditions Extensive training and friendly team Competitive salary and advantages package Opportunities for personal and professional growth 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 career development and success.

📌 Study Startup Specialist Ii Mississauga
🏢 PSI
📍 Mississauga