Regulatory Affairs Senior Specialist
hace 4 semanas
Regulatory Affairs Senior Specialist - Homebased in Estonia ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Regulatory Affairs Specialist to join our diverse and dynamic team. As a Regulatory Affairs Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing Undertaking variable duties based on project requirements, primarily within Pharmaceutical, Biotechnology, or Biologics Regulatory Affairs, with potential involvement in related areas. Contributing to regulatory submissions team activities, including preparation, compilation, and submission of regulatory documents such as CT/IND, MAA/NA, variations/lifecycle submissions, DSUR, PSUR, renewals, and agency briefing documentation. Managing and implementing label review, translation requirements, fee calculations, and other aspects for regulatory submissions. Providing input to the Regulatory Intelligence function and participating in readability testing. Reviewing IMPD/IB Core Docs and labeling for clinical trials. Collaborating with Regulatory Submissions team or cross-functional teams based on project size and nature. Facilitating business development activities as needed. Your profile Bachelor's degree in a scientific or healthcare-related field; advanced degree preferred. Minimum of 2-3 years of experience in regulatory affairs within the pharmaceutical or biotechnology industry. Proficiency in regulatory submission processes and requirements, including CT/IND, MAA/NA, variations, DSUR, PSUR, and renewals. Familiarity with label review, translation requirements, and regulatory intelligence activities. Strong attention to detail and excellent communication skills. What ICON can offer you Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply #J-18808-Ljbffr
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Regulatory Affairs Specialist – Consultant
hace 1 semana
Mexico City ClinChoice A tiempo completoRegulatory Affairs Specialist – Consultant 6 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both...
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Regulatory Affairs Specialist – Consultant
hace 1 semana
Mexico City ClinChoice A tiempo completoRegulatory Affairs Specialist – Consultant 6 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both...
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Strategic Regulatory Affairs Manager
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Mexico City Eli Lilly and Company A tiempo completoA leading global healthcare company is seeking a Regulatory Affairs Manager in Mexico City. This mid-senior level role is responsible for managing regulatory affairs activities for new product registrations and ensuring compliance with local regulations. The ideal candidate will have robust regulatory expertise, experience in team supervision, and the...
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Manager, Regulatory Affairs
hace 5 días
Mexico City Gilead Sciences, Inc. A tiempo completoManager, Regulatory Affairs page is loaded## Manager, Regulatory Affairsremote type: Onsite Requiredlocations: Mexico - Mexico Citytime type: Full timeposted on: Posted Todayjob requisition id: R0049729At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis,...
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Manager, Regulatory Affairs
hace 5 días
Mexico City Gilead Sciences A tiempo completoAt Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges,...
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Manager, Regulatory Affairs
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Mexico City Gilead Sciences A tiempo completoAt Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges,...
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Manager, Regulatory Affairs
hace 3 días
Mexico City Gilead Sciences, Inc. A tiempo completoAt Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges,...
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Manager, Regulatory Affairs
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Mexico City Gilead Sciences, Inc. A tiempo completoAt Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges,...
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