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 professional 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 benefits package Opportunities for personal and professional growth For this position, PSI is not hiring individuals who require work visa sponsorship for employment now or in the future.

Make the right call and take your career to a whole recent level.

Join the company that focuses on its people and invests in their professional development and success.

📌 Study Startup Specialist II (Mississauga)
🏢 PSI CRO
📍 Mississauga