Senior Clinical Trial Manager

Clinical Trial Manager (Clinical Research Medical Advisor) - FSP - Homebased - ItalyUpdated: Clinical Trial Manager (Clinical Research Medical Advisor) - FSP - Homebased - ItalySyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.supportive and engaged line management; technical and therapeutic area training; Clinical Trial Manager (Clinical Research Medical Advisor) is responsible for providing medical and scientific leadership to ensure the high-quality execution of clinical trials and studies in the assigned country or cluster. This role bridges Clinical Development and cross-functional teams, ensuring local medical input and compliance with regulatory standards.Key ResponsibilitiesLead local clinical/medical aspects of trial implementation, including protocol review, site selection support, feasibility assessments, and recruitment strategy planning.Act as the medical representative to support study design, regulatory interactions, and site training to ensure protocol adherence and patient safety.Identify pro actively recruitment challenges or operational challenges and develop migration plans.Provides protocol/compound and indication trainings to internal and external partnersProvide medical input for Informed Consent Forms (ICFs) and safety reporting.Partner with clinical operations, regulatory, medical affairs, and external experts to optimize trial execution.Support safety oversight: review serious adverse events (SAEs), provide pharmacovigilance support, and ensure clinical data quality.Contribute to early trial start-up by validating study feasibility and supporting site engagement and training.Provide clinical/medical expertise for regulatory inspections, audits, and trial documentation.May work cross countryQualificationsEducation:Medical Doctor Degree is essentialPharmaD or PhD could be relevant in case of solid experience as Medical Science Liason/AdvisorLanguage:Local Language fluency requiredFluent in English (speaking and writing)Experience:Minimum 3 years in clinical development or clinical practice in the pharmaceutical or healthcare sector.Strong understanding of clinical trial design, implementation, and ICH/GCP principles.Excellent presentation skills in English and local language.Understanding of safety and regulatory requirements in clinical trials.Experience supporting regulatory submissions, Audits and inspections.Travel RequirementUp to 50% travelGet to know Syneos HealthOver the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.Learn more about Syneos Health. Further, nothing contained herein should be construed to create an employment contract. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.SummaryRoles within the Clinical Trial Management job family are responsible for all aspects of the development, coordination, and implementation of Phase 1 clinical research studies at the organization's facilities. Collaborates with the principal investigator, liaisons between research subjects, client teams, investigators, and clinic operations teams, and plans logistics and resource usage. Tracks study progress in alignment with project milestones, client deliverables, and budget, and follows applicable regulations globally and by region.Impact and ContributionIncludes executives as well as managers, supervisors and team leads providing strategic vision and/or tactical direction across a discipline and/or broader organization. The majority of time is spent overseeing their area of responsibility, planning, prioritizing, and/or directing the responsibilities of employees. Goal are achieved through management of process, policy, and performance of direct and/or indirect reports. Delivers operational results that have direct impact on immediate or short-term department results. Requires practical knowledge in managing the execution of processes, projects and tactics within team.At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. We also encourage you to join our Talent Network to stay connected to additional career opportunities.We work hard,and smart, all in the name of getting much-needed therapies to thosewho need them most. A career with Syneos Health means your everyday work improvespatients' lives around the world. Selecting us as an employer secures a career inwhich you're guaranteed to:Syneos Health (Nasdaq: SYNH) is a leading integrated biopharmaceutical solutionsorganization built to accelerate customer success. We translate unique clinical,medical affairs and commercial insights into outcomes to address modern marketrealities. Phone: 919 876 9300Fax: 919 876 9360Toll-Free: 866 462 7373Syneos Health is an Equal Opportunity Employer. All qualified applicants will receiveconsideration for employment without regard to race, color, age, religion, marital status,ethnicity, national origin, sex, gender, gender identity, sexual orientation, protectedveteran status, disability or any other legally protected status and will not bediscriminated against.