Company Description Seriant (formerly the Montreal Health Innovations Coordinating Center, MHICC) is a full-service Clinical Research Organization (CRO) that has partnered with pharmaceutical, medical device, biotech, and academic institutions for over 25 years. Based in Montreal and operating internationally, Seriant supports all phases of clinical trials across a wide range of therapeutic areas, with a strong foundation in cardiology and growing expertise in precision medicine.

The organization is dedicated to bringing creative therapies to life and creating meaningful impact for patients worldwide. Seriant offers a comprehensive portfolio of services, including project management, clinical operations and monitoring, biostatistics and programming, data management, regulatory affairs, medical and safety oversight, pharmacovigilance, medical and scientific writing, quality assurance, and specialized capabilities such as biobank, pharmacogenomics, and medical devices and wearables. Seriant maintains an unwavering commitment to excellence, collaboration, and the advancement of clinical research.

Role Description The Clinical Project Manager is a full-time, hybrid role based in Montreal, QC, with flexibility for partial work from home. This role oversees the planning, execution, and completion of clinical trials, ensuring that studies are delivered on time, within scope, and in compliance with regulatory and ethical standards.

Day-to-day responsibilities include leading cross-functional project teams, managing study timelines and budgets, coordinating clinical operations and trial activities,



and maintaining effective communication with sponsors, investigators, and internal stakeholders.

The Clinical Project

Manager reviews and contributes to study protocols and related documentation, monitors project risks and issues, and implements corrective actions as needed. The role also involves supporting quality assurance processes, contributing to continuous improvement of project management practices, and mentoring team members to promote best practices in clinical research.

Qualifications

- Strong Trial Management and Clinical Operations skills, with experience overseeing multi-center clinical studies.
- Demonstrated Project Management expertise, including planning, budgeting, risk management, and stakeholder communication.
- Solid Research capabilities, including familiarity with clinical research methodologies, Good Clinical Practice (GCP), and regulatory requirements.
- Ability to review, interpret, and contribute to Protocol development and related clinical trial documentation.
- Bachelor’s or Master’s degree in life sciences, health sciences, pharmacy, or a related field; PMP or equivalent certification is an asset.
- Several years of experience in clinical project management within a CRO, pharmaceutical, medical device, or academic research environment.
- Excellent organizational, analytical, and problem-solving skills, with attention to detail and a focus on quality.
- Strong written and verbal communication skills in English; proficiency in French is an advantage.
- Ability to work effectively in a hybrid environment, collaborate with cross

📌 Clinical Project Manager (Montreal)
🏢 Seriant (formerly MHICC)
📍 Montreal