The Start-Up Manager is responsible for overseeing and managing the successful and timely activation of clinical trial sites across multiple countries. This role leads all start-up activities, ensures regulatory compliance, and collaborates with cross-functional teams to meet study timelines and client expectations. The ideal candidate will bring strategic insight, operational excellence, and strong leadership to drive efficient and high-quality site activation.
More specifically, the Start-Up, Project Manager
- Manage the end-to-end study start-up process, including site selection, regulatory submissions, site contracting and budgeting, and site activation.
- Define start-up strategy and timelines in collaboration with the Project Manager and cross-functional leads.
- Prepare and maintain a site activation plan, ensuring selected sites and countries optimize opportunities for successful study delivery.
- Proactively identify and communicate issues impacting delivery and providing proposed solutions.
- Monitor progress against these timelines and proactively address delays or risks.
- Oversee and coordinate each step of the start-up process to ensure activation goals are met.
- Serve as the primary liaison among all functions involved during the start-up period, ensuring effective cross-functional communication and collaboration.
- Track and report start-up performance metrics, providing transparency and accountability.
- In partnership with PM, lead client-facing calls and serve as the main point of contact for start-up activities with both internal teams and Sponsors.
Requirements
- Bachelor’s degree in Life Sciences, Nursing, or related field (Master’s preferred).
- Minimum of 3+ years of experience in clinical trial start-up, with demonstrated leadership experience.
- Proven ability to manage multi-country start-up activities and cross-functional teams in a matrixed environment.
- Excellent project management, communication, and problem-solving skills. Ability to manage multiple priorities in a fast-paced, deadline-driven environment.
Our company
The work environment
At Indero, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.
In this position, you will be eligible for the following perks:
- Flexible work schedule
- Permanent full-time position
- Company benefits package
- Ongoing learning and development
About Indero
Indero is a contract research organization (CRO) specialized in dermatology and rheumatology. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Indero continues to grow and expand in North America and Europe.
Indero is committed to providing equitable treatment and equal opportunity to all individuals. As such, Indero will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.
Indero only accepts applicants who can legally work in Spain.
Description - Fr
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Profil recherché
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Notre entreprise
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Top Skills
What We Do
As a CRO (Contract Research Organization) specialized in dermatology and rheumatology, we provide scientific guidance, accurate results and customer satisfaction. Our unique service offering combines specialized Contract Research Services, knowledge of dermatology sites in North America and Europe reach and the extended capabilities of a large clinical research site.
The design and conduct of Phase I to Phase IV studies is our core expertise.
Our specialized services include:
• Study Design and Protocol Development
• Submission to Regulatory Agencies and Central Ethics Committees
• Regulatory Consulting
• Trial Master Files Management
• Project Management
• Investigator / Site Selection
• Patient Recruitment
• Clinical Monitoring
• Medical Monitoring
• Pharmacovigilance
• Data Management
• Biostatistical Analysis
• Clinical Study Report
• Medical Writing / Publication
Since 2000, Innovaderm has built a strong reputation for the quality of its research and the care offered to its study participants, its clients and its sites, often exceeding our client’s timeline expectations.
