Overview
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. There will be opportunities to develop and enhance technical and personal skills through cross collaboration with a highly experienced team. In this impactful and visible position, the role holder will add value to SynOx during a critical time of its evolution as well as making a difference to patients.
About SynOx Therapeutics
SynOx Therapeutics is a privately owned innovative, late-stage biopharmaceutical company. 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. By connecting our industry-leading knowledge and experience with passion and dedication, we initially aim to provide life-improving options to address the unmet clinical needs of people living with tenosynovial giant cell tumors (TGCT) and other macrophage-mediated diseases.
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.
SynOx is starting a Phase 3 registration trial in TGCT and will also initiate Phase 2 PoC studies in other indications. SynOx is led by an experienced team of industry professionals with a successful track record of developing and bringing products to commercialisation. It is backed by a strong syndicate of premier life sciences investors.
Position Overview
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.
Responsibilities include but are not limited to:
- Project Planning and Execution
- Stakeholder Management
- Quality Assurance and Compliance
- Resource Management
- Documentation and Reporting
Key Requirements (Experience & Skills)
- Degree in life sciences, nursing, pharmacy, or related field; advanced degree preferred.
- 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.
- Strong leadership abilities, with experience leading cross-functional teams and managing diverse stakeholders.
- Excellent communication skills, with the ability to effectively convey complex information to both technical and non-technical audiences.
- 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., CCRA) is a plus.
- Ability to travel as needed for project meetings, site visits, and conferences
- ‘Self-starter’ – be highly organised, proactive and efficient. Whilst we are a highly experienced team with cross functional experience, there will be a high level of autonomy in this role.
- Strong verbal and written communication skills.
- Ability to build and maintain strong and collaborative internal and external relationships.
- Happy to ‘roll up their sleeves’ and get involved with any business needs even if they do not fall directly within the scope the role (as is often the case in start-up environment).
- Enjoy working in a small start-up team.
Location: Remote UK (preference) possibly Ireland or Netherlands, with travel – as required
Salary: Competitive- depending on experience
Working arrangement: Full time employment, however, we are happy to discuss any flexible working preferences and consider part-time candidates.
For more information, a confidential conversation or to send your CV please contact: recruitment@synoxtherapeutics.com
In your application, please detail your specific experience relating to Phase 3, rare diseases/oncology indications and biopharmaceutical/biotechnology start-up environment.
SynOx Therapeutics does not accept speculative CVs / applications from recruitment agencies or unsolicited contact to our team members.
This job was originally posted as: https://thecareerwallet.com/stats/track/MTUyNjc3NzYyNC18LTE0NS18LTcw