Do you dare to shake up the medical world and improve the lives of patients with chronic degenerative diseases?Allegro is a revolutionary start-up that designs and develops ground-breaking biomedical nanotechnology for the treatment of osteoarthritis. We wish to hire a: Clinical SpecialistThe JobWe are seeking a hands-on scientist with a passion for life sciences to join our team as Clinical Specialist. As a Clinical Specialist, you work directly with the CSO and RM of the company. You will actively perform:- Clinical Strategy- Medical writing- Project managementResponsibilities:· Lead the Clinical Developmentment Strategy: Design and refine clinical development plans in alignment with corporate objectives and regulatory pathways, with a focus on value generation and risk mitigation.· Write Study Protocols : Collaborate with scientific, regulatory, and commercial teams to design high-quality clinical studies that address unmet medical needs and support product positioning.· Medical and Scientific Writing: Draft and review essential clinical documents, including study protocols, investigator brochures, clinical study reports (CSRs), (e.g., CER/LRR/PSUR).· Cross-Functional Project Management: Lead clinical project planning and execution, ensuring alignment across departments (R&D, regulatory, medical, and commercial) and timely delivery of milestones.· Stakeholder and Vendor Coordination: Manage interactions with external partners such as CROs, KOLs, investigators, and consultants to ensure efficient and high-quality execution of clinical activities.· Risk and Quality Oversight: Proactively identify clinical and operational risks, implement mitigation strategies, and uphold quality standards across deliverables.· Clinical Budget and Resource Oversight: Support budgeting processes, ensuring efficient allocation and tracking of clinical resources in line with project timelines and scope.· Regulatory and Ethical Compliance: Ensure that all clinical activities are conducted in accordance with ICH-GCP, relevant regulations, and internal policies.· Site Engagement and Education: Act as the primary liaison for study centers and clinical investigators—motivating and supporting them through clear communication, site visits, and ongoing education to ensure smooth study initiation and conduct.Requirements:· Minimum of 10 years of experience in medical writing, clinical strategy and clinical trial management, preferably in the medical device industry and/or within the field of osteoarthritis.· In-depth knowledge of ISO 14155, including FDA and MDR guidelines, and experience with regulatory submissions and leading clinical audits.· Exceptional (medical) writing skills· Strong analytical and strategic insights, and the ability to understand how your strategic choices translate to other domains (operations, statistics, regulatory...)· Strong project management skills with the ability to effectively prioritize tasks and manage multiple projects simultaneously.· Excellent communication and interpersonal skills, with the ability to collaborate effectively with internal and external stakeholders.· Proven leadership abilities, including the ability to lead cross-functional teams and motivate team members to achieve project goals.· Detail-oriented with strong analytical and problem-solving skills, capable of identifying and resolving issues in a timely manner.· Proficiency in Microsoft Office Suite and experience with clinical trial management systems (CTMS) and electronic data capture (EDC) platforms.Your ProfileYou have a:· Master's degree in biomedical sciences, medicine, or another life sciences degree.· Additional training and certificates in clinical research, regulatory science, or business is a plus.· English CEFR C2 (Mastery level)· Proven track record in designing and executing clinical studies, preferably in an international setting.You have the following skills:· Deep understanding of clinical development processes, including GCP, ICH guidelines, and regulatory requirements (EMA/FDA).· Demonstrated experience in writing and reviewing core clinical documents: protocols, IBs, CSRs, and regulatory dossiers.· Strong grasp of medical and scientific literature and ability to translate complex data into strategic and operational plans.· Experience leading cross-functional clinical teams and managing external partners (CROs, consultants, investigators).· Skilled in project planning, timeline tracking, and budget oversight in a matrixed environment.· Ability to identify risks, solve problems, and adapt in a fast-moving, dynamic organization.· Excellent interpersonal skills with a proven ability to build and maintain productive relationships with clinical sites, investigators, and KOLs.· Experience training or educating site personnel and motivating them throughout the trial lifecycle is highly valued.· Strong written and verbal communication skills; capable of presenting clinical strategy and study progress to internal leadership, boards, and external stakeholders.· Comfortable working in small, agile teams with high accountability and autonomy.· Experience in musculoskeletal, inflammation, or neurology clinical trials is a plus.· Familiarity with biotech startup environments and willingness to wear multiple hats when needed.· Science-driven, business-focused: applying state-of-the-art innovation to achieve strategic goals within a business context.· Analytical Skills: Demonstrate strong analytical and problem-solving abilities, with the capacity to leverage data and insights to drive informed decisions.· Planning and organization: work in a very well-structured manner· Meticulous perfection meets operational performance: a unique ability to deliver the highest quality work in short timelines.· Communication and Relationship Building: Exhibit excellent communication skills, both verbal and written.· Strategic Thinking: Display a strategic mindset and the ability to envision long-term goals while effectively managing day-to-day operations. Stay updated on industry trends and best practices to drive innovation.Our offeringAs a companyAn impact- and purposeful environment, in a young start-up that can change the lives of many people suffering from osteoarthritis.A high-performance and eager culture, An easy and uncomplicated team, but very eager and high-performance.An opportunity to learn a lot, and grow together with the company, make a positive impact, and build tomorrow’s future. The job allows for an ambitious person to build a great career as a top executive.For you· A great remuneration package with a substantial salary.· Company car.· Extra-legal benefits (hospitalization insurance, meal vouchers, ...)· Premium working tools.You are stationed in Liège with flexible home office.ContactDo you want to join the future? Contact us via e-mail:· Info@allegro.bio· Subject: Clinical Specialist