Clinical Project Manager

2 weeks ago


United Kingdom SynOx Therapeutics Full time

Clinical Project Manager   This is an excellent opportunity for an experienced clinical operations project leader to use their holistic clinical trials experience to a fast moving, outsourced environment and apply a strong risk management approach to complex rare disease trials. It was established in November 2020 following the licensing from Roche exclusive worldwide rights to Emactuzumab, a potentially best-in-class CSF-1R monoclonal antibody.

Our mission is to establish Emactuzumab as a best-in-class drug of choice to address the unmet needs and improve the quality of life of as many patients as possible. Emactuzumab has a well-tolerated safety profile and has shown promising efficacy in patients suffering from TGCT, a rare and debilitating disease that causes significant pain and disability.

It is backed by a strong syndicate of premier life sciences investors. 
 
The Clinical Project Manager in collaboration with the Senior Global Study Director will play a pivotal role in managing clinical trials and projects, ensuring adherence to timelines, budgets, and quality standards. This position requires strong project leadership skills, excellent communication abilities, and a deep understanding of clinical trial processes and regulations. 

Project Planning and Execution 
Quality Assurance and Compliance 
Degree in life sciences, nursing, pharmacy, or related field; Several years of experience in clinical project management with a proven track record of successfully managing complex trials from initiation to closeout 
~ Strong preference for a background in a biopharmaceutical/biotechnology start-up environment 
~ Phase 3 experience, preferably in rare disease and/or oncology indications 
~ In-depth knowledge of clinical trial processes, regulatory requirements, and industry best practices. 
~ Proficiency in project management tools and software, such as Microsoft Project, Excel, and electronic data capture systems. 
~ Certification in project management (e.g., PMP) and/or clinical research (e.g., Ability to travel as needed for project meetings, site visits, and conferences 
~ ‘Location: Remote UK (preference) possibly Ireland or Netherlands, with travel - as required 
Salary: Competitive- depending on experience 

Full time employment, however, we are happy to discuss any flexible working preferences and consider part-time candidates. 
 
In your application, please detail your specific experience relating to Phase 3, rare diseases/oncology indications and biopharmaceutical/biotechnology start-up environment. 



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