Study Startup Specialist II

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3.000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you. 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 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 Qualifications 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. 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 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.

Lead the study activation process on a country level, ensuring that clinical research projects start smoothly and on time. Collaborate with project teams for site activation, facilitate agreements, and coordinate necessary documentation.

A college or university degree in Life Sciences or equivalent experience is required, along with at least 2 years of full-scope study startup experience. Proficiency in English and French, along with strong communication and organizational skills, is also necessary.

• Excellent Working Conditions • Extensive Training • Friendly Team • Competitive Salary • Benefits Package • Opportunities For Personal And Professional Growth

• Gestion de projetSouhaitée

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Communication
• Organizational Skills
• Negotiation
• Relationship Building
• Site Activation
• Contract Negotiation
• Budget Negotiation
• Document Submission
• Project Coordination
• Clinical Research
• IRB Submission
• Investigational Product Distribution
• Timeline Development
• Enrolment Projections
• Issue Escalation

• Healthcare
• Science & Research
• Administrative
• Manufacturing

Formation minimale

Baccalauréat

Expérience minimale

2+ ans

Postuler avant le

13 août 2026

Langue de l’offre

anglais

Heures de travail

40 heures par semaine

Exigences de lieu

Country, Mississauga, Ontario, Canada

Niveau d’expérience

Associate

Mode de candidature

La candidature directe est offerte