Country Study Operations Manager (Sponsor Dedicated) Homebased, Turkey

Country Study Operations Manager (Sponsor Dedicated) Homebased, TurkeySyneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. 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 deliver – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. • We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Job ResponsibilitiesDevelop and coordinate Phase 1 clinical research studies, ensuring all aspects of the study are meticulously planned and executedImplement clinical research protocols and ensure compliance with regulatory requirements, including Good Clinical Practice (GCP) guidelinesCollaborate with principal investigators, research subjects, client teams, and clinic operations teams to facilitate smooth communication and coordinationPlan and manage logistics and resource usage for clinical trials, including scheduling, budgeting, and resource allocationTrack study progress and ensure alignment with project milestones, client deliverables, and budget, providing regular updates to stakeholdersPrepare and present study reports and updates to stakeholders, including detailed analysis of study data and progressEnsure adherence to global and regional regulations and guidelines, staying up-to-date with any changes or updatesProvide guidance and support to lower-level professionals and team members, fostering a collaborative and supportive work environmentIdentify and resolve any issues or challenges that arise during the course of the study, ensuring timely and effective solutionsMaintain accurate and comprehensive documentation of all study-related activities, ensuring transparency and accountabilityQualifications:Bachelor's degree in a related field (e.g., life sciences, clinical research)Minimum of 3 years of experience in clinical trial management or a related fieldIn-depth knowledge of clinical research processes and regulationsStrong project management and organizational skillsExcellent communication and interpersonal skillsAbility to work independently and as part of a teamProficiency in using clinical trial management software and toolsCertifications:Certified Clinical Research Professional (CCRP) or equivalent certification preferredNecessary Skills:Strong analytical and problem-solving skillsAttention to detail and accuracyAbility to manage multiple projects and priorities simultaneouslyProficiency in Microsoft Office Suite (Word, Excel, PowerPoint)Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirementsGet 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.No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.http://www.syneoshealth.comAdditional InformationTasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally,