-We use cookies to offer you a better browsing experience, analyze site traffic, and personalize content. Read about how we use cookies and how you can control them by visiting our Cookie Settings page. If you continue to use this site, you consent to our use of cookies. Cookie Settings AllowSearch for Job TitleEnter LocationSearchCountry Approval SpecialistLocation Remote, Argentina Job Id R-01359882 Job Type Full time Category Clinical Research Remote Fully RemoteAdd To Cart Apply Now Share via email Share via Facebook Share via LinkedIn Share via twitter Our team of colleagues in clinical research services are at the forefront of getting cures to market. We bring a high caliber of scientific and clinical expertise to the development of drugs that address the world’s most challenging health concerns. Our Clinical Research team, who powers our PPD® clinical research portfolio, are part of our leading general contract research organization (CRO).Accessibility/Disability Access We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Learn more Equal Opportunity Policy Statement Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to any characteristic protected by local, state, or federal laws, rules, or regulations. Learn more Get notified for similar jobsYou'll receive updates once a weekEnter Email address (Required)Activate Manage alerts Get tailored job recommendations based on your interests.Get StartedSimilar Jobs Country Approval Specialist Location Remote,



Argentina Job Id R-01359881 Embrace the role of a Country Approval Specialist and play a vital role in managing and coordinating regulatory submissions for leading pharmaceutical and biotech companies. Leverage your expertise in local and integral regulatory compliance to ensure timely site activations and successful project outcomes. Grow your career in a dynamic, collaborative environment. Country Approval Spec Location Remote, Argentina Job Id R-01355347 Embrace the role of a Country Approval Specialist and play a vital role in managing and coordinating regulatory submissions for leading pharmaceutical and biotech companies. Leverage your expertise in local and global regulatory compliance to ensure timely site activations and successful project outcomes. Grow your career in a dynamic, collaborative environment. Country Approval Specialist / Sr Country Approval Specialist Available in 5 locations Job Id R-01358140 Join our team as a Senior Country Approval Specialist and play a pivotal role in clinical trial start-up and regulatory submissions. Collaborate with global teams, ensure compliance with local and international regulations, and help advance innovative therapies. If you have strong clinical research experience and a passion for quality, we want to hear from you! Clinical Team Manager (CTM) – HemOnc Available in 6 locations Job Id R-01353398 Embrace the opportunity to become a Clinical Trial Manager and drive the success of innovative clinical studies. Oversee operational and quality aspects, ensure regulatory compliance, and lead a dynamic team to deliver impactful results. If you have strong leadership skills and a passion for clinical excellence, this is your opportunity to make a difference. Clinical Team Manager (CTM) – HemOnc Available in 6 locations Job Id R-01353399 Embrace the opportunity to become a Clinical Trial Manager and drive the success of innovative clinical studies. Oversee operational and quality aspects, ensure regulatory compliance, and lead a dynamic team to deliver impactful results. If you have strong leadership skills and a passion for clinical excellence, this is your opportunity to make a difference. Show more

📌 Country Approval Specialist (Chicligasta)
🏢 Thermo Fisher
📍 Chicligasta