Sr. Manager, Study Start-Up
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| Company Name | Alimentiv |
| Company Type | Private |
| Job Type | Full-Time |
| Salary Range | €76,500.00/yr – €127,000.00/yr |
| Location | Warsaw, Mazowieckie, Poland |
| Qualifications | None / No Formal Education |
| Experience | 10 Year+ |
Job Overview
Alimentiv is seeking a highly experienced Sr. Manager, Study Start-Up to lead the initial phase of clinical trials, ensuring efficient and compliant study activation. Based in Warsaw, Mazowieckie, Poland, you will play a critical role in accelerating the development of life-changing therapies.
Company Overview
Alimentiv is an industry-leading specialty GI contract research organization (CRO) dedicated to transforming clinical trial outcomes and accelerating the development of life-changing therapies. We integrate deep GI expertise, advanced medical imaging, clinical operation excellence, and cutting-edge precision medicine/laboratory services. With a global network of 5,000+ sites in over 60 countries, Alimentiv expedites study activation and maximizes patient enrollment for efficient clinical trials. Trusted by pharmaceutical and biotech partners, we support over 70% of all IBD compounds in development today, delivering customized end-to-end solutions. Our comprehensive services include Clinical Trial Services, Medical Monitoring, Medical Imaging, Medical Research & Development, Medical Writing, Precision Medicine/Biomarkers, Clinical Pharmacology, Histopathology, Spatial Biology, Statistics, and Real-World Evidence. Headquartered in London, Ontario, Alimentiv operates globally across Canada, the US, Europe, Asia-Pacific, and Latin America.
Quick Details
- Salary Range: €76,500.00/yr – €127,000.00/yr
- Job Type: Full-time
- Qualifications: none
- Experience: 10 Year+
Key Responsibilities
- Lead and manage the study start-up process for complex clinical trials from initiation to site activation.
- Develop and implement robust study activation strategies to ensure timely and efficient study launches.
- Oversee regulatory submissions, ethics committee approvals, and essential document collection.
- Collaborate effectively with cross-functional teams including clinical operations, project management, and legal.
- Ensure strict adherence to all relevant regulatory guidelines, company SOPs, and industry standards.
- Mentor and provide guidance to junior study start-up personnel, fostering their professional development.
Requirements
- Extensive experience in clinical trial study start-up within a Contract Research Organization (CRO) or pharmaceutical setting.
- Proven leadership and project management skills with a track record of successful study initiations.
- Thorough understanding of international clinical trial regulations (e.g., ICH-GCP) and ethical guidelines.
- Excellent communication, negotiation, and problem-solving abilities.
- Ability to work effectively in a fast-paced, global, and multicultural environment.
- Strong organizational skills, attention to detail, and ability to manage multiple priorities.
Benefits
- Competitive salary package and performance-based bonuses.
- Comprehensive health, dental, and vision insurance plans.
- Opportunities for professional growth, training, and career advancement within a global CRO.
- Work in a collaborative, innovative, and supportive team environment.
- Contribute to the development of life-changing therapies and make a significant impact on patient lives.
- Access to employee wellness programs and initiatives promoting work-life balance.