NonStop Consulting
NonStop Consulting, on behalf of a client, is seeking a Senior Clinical Scientist – Medical Strategy to join and play a foundational role in the launch of a newly established Medical Affairs department.
This high-impact position blends deep scientific expertise with strategic business vision. Reporting directly to the CEO, you will not only lead the clinical research agenda but also help define the long-term direction of the Medical Affairs function.
As the first hire in this new unit, you will have a unique opportunity to shape processes, partnerships, and scientific messaging from the ground up.
You will oversee the end-to-end management of clinical studies that demonstrate the safety and efficacy of advanced probiotic and nutraceutical solutions, while also developing scientific content to support internal stakeholders and external communication.
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Key Responsibilities
Clinical Research Leadership
- Design, lead, and manage 5-6 clinical trials per year (sponsored and investigator-initiated).
- Draft and review protocols, informed consent forms, and relevant regulatory documentation.
- Coordinate CROs and clinical sites to ensure on-time, compliant trial execution.
- Ensure full compliance with international regulatory frameworks (GCP, FDA, EMA).
Scientific & Medical Affairs
- Serve as the primary scientific liaison across internal teams and external partners.
- Participate in strategic meetings with clients and stakeholders to align on clinical goals.
- Translate clinical insights into robust development strategies.
- Provide scientific support during sales or business development presentations.
Medical Communication & Content Development
- Lead the creation of high-quality scientific materials for internal and external use.
- Develop manuscripts, abstracts, and presentation content for scientific publications and conferences.
- Partner with Marketing to ensure scientific integrity in promotional and communication materials.
Strategic Development & Network Expansion
- Identify and assess opportunities for new clinical collaborations and trials.
- Collaborate with R&D and Regulatory Affairs to align clinical research with innovation goals.
- Establish and oversee research grants in coordination with senior scientific leadership.
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Required Qualifications
Education & Experience
- Advanced degree (PhD, MD, PharmD, or equivalent) in Life Sciences, Medicine, or related discipline.
- 5+ years of clinical trial management experience, ideally within probiotics, nutraceuticals, or pharma.
- Demonstrated excellence in medical writing and scientific communications.
Technical Skills
- In-depth knowledge of clinical trial design, execution, and regulatory requirements.
- Familiarity with microbiome science and probiotic research is strongly preferred.
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Language & Travel
- Fluent in English (written and spoken); Italian is a strong asset.
- Availability to travel nationally and internationally (~20%) for site visits and meetings.
What we offer
- Flexible working hours and one day of remote work per week.
- An exciting opportunity to grow within an innovative, fast-growing company and take on a strategic role with real impact!
