CRA II

CRA II - Sponsor Dedicated - Based in Paris- client based or home-basedUpdated: October 15, 2025Location: FRA-RemoteJob ID: 25102557DescriptionCRA II - Sponsor dedicated - Based in Paris- client based or home-basedSyneos 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.Why Syneos HealthWe 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 our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.Job ResponsibilitiesConduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report formsDevelop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templatesContribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materialsManage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issuesEnsure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow‑up letters, and action plansCollaborate with cross‑functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conductQualificationsBachelor's degree in a related field or equivalent experienceMinimum of 2-4 years of experience in clinical research monitoringStrong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirementsExcellent communication and interpersonal skillsAbility to work independently and manage multiple prioritiesProficiency in using clinical trial management systems and other relevant softwareCertificationsCertified Clinical Research Associate (CCRA) or equivalent certification preferredNecessary SkillsAttention to detail and strong analytical skillsProblem‑solving abilities and critical thinkingAbility to work effectively in a team environmentStrong organizational and time management skillsProficiency in Microsoft Office SuiteGet 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.Contact InformationPhone: 919 876 9300Fax: 919 876 9360Toll‑Free: 866 462 7373Equal Opportunity EmployerSyneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against. If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, including the use of this website, please contact us at: Email: jobs@syneoshealth.com One of our staff members will work with you to provide alternate means to submit your application. #J-18808-Ljbffr