Senior Clinical Studies Associate
Listed on 2026-01-10
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Healthcare
Clinical Research, Medical Technologist & Lab Technician, Medical Science
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Senior Clinical Studies AssociatePublished on:
Jan 6, 2026
Country:
United States
Job Category:
Research & Development
Employment type:
Regular Full Time
Join Diasorin?Impactful Work:
When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world.Global Reach & Innovation:
Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry.Diverse and Inclusive Culture:
We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive.Join Our Team:
If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward.Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare.
Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact!
Job Scope
The position oversees the clinical trial process for new diagnostic products. The process includes participating in the development of clinical trial protocols, establishing the capabilities required for the clinical trial sites to complete the protocols, identifying sites having the proper clinical trial capabilities, managing the clinical trial contract process, and managing the clinical trial sites for compliance. Training of clinical trial sites and internal departments such as Technical Services may be required.
Coordinating the logistics of sample and data transfer as well as cost accounting of the clinical trial process will be performed. The post-clinical trial activities of this position include coordinating cross-functional teams to launch a new product or device, ensure publications and white papers are available, and assist in the pre-market positioning of the new product. The clinical trial sites may be either domestic or international, so periodic field travel can be expected.
Supports applicable regulations including ISO, Local, State, and/or Federal requirements.
Job Responsibilities and Duties
- In collaboration with other Dia Sorin staff, identify potential external sites for the evaluation of new Dia Sorin IVDs and performance of clinical trials.
- Perform detailed investigations, including site visits, to evaluate the technical capability of potential external collaborators.
- Participate in the development of clinical trial protocols, which will include evaluation of the individual site’s technical and logistical capabilities to perform the protocols.
- Initiate contract negotiations with external collaborators and present to the appropriate Dia Sorin personnel for final signature. Periodically review the sites for contract compliance during the clinical trial process.
- Coordinate and manage the clinical specimen acquisition process.
- Coordinate any training required at external collaboration sites, which may include providing on-site training.
- Act as the primary contact person between Dia Sorin and external collaborators for the…
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