Regulatory Affairs Specialist
hace 4 días
As a Regulatory Affairs Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.**What you will be doing**:- Regulatory advice to drug development is key to ensuring our clients pursue first time right strategies to overall product development and to clinical programme development.**You are**:- Scientific (any science discipline)or Pharmacy degree- Regulatory specialist could come from any ICON department (especially ICO, Clin ops) if you have prior regulatory experience in Agency, CRO or Pharma Industry or from the role of SSUA.- English fluent ,write & read**Why ICON?**Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
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Regulatory Affairs Specialist
hace 3 semanas
Desde casa, México ProductLife Group A tiempo completoIn the context of a new project, we are looking for a Regulatory Affairs Specialist to join our teams in Mexico.**Responsibilities**:Provide guidance and support about Mexican and Central America legislationContribute to the regulatory activities performed. Regulatory activities include pre licensing activities, new registration (sites and medicinal...
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Regulatory Affairs Specialist
hace 3 semanas
Desde casa, México ProductLife Group A tiempo completoIn the context of a new project, we are looking for a Regulatory Affairs Specialist to join our teams in Mexico/LATAM.**Responsibilities**:Provide guidance and support about Mexican and Central America legislationContribute to the regulatory activities performed. Regulatory activities include pre licensing activities, new registration (sites and medicinal...
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Regulatory Affairs Specialist, Latam
hace 3 semanas
Desde casa, México IQVIA A tiempo completo**POSITION TITLE**: Regulatory Affairs Specialist**REPORTS TO**: Manager, Regulatory Affairs or Designee**BASIC FUNCTIONS**:**ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES**:- Assist Manager, Regulatory Affairs, in assuming primary or secondary regulatory responsibility for assigned clinical research projects by providing regulatory information,...
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Associate Director, Regulatory Affairs
hace 4 días
Desde casa, México IQVIA A tiempo completo**We are looking for a forward-thinking, metrics-driven leader with study start-up experience, who has served as a Department Head and brings cross-functional and strategic expertise. This role will involve managing 8-10 direct reports and requires strong financial acumen to drive success.**Job OverviewLine Management responsibilities for a team of...
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Regulatory Affairs Manager
hace 3 semanas
Desde casa, México Atnahs A tiempo completo**Based in Mexico (remote)**:**Salary: Competitive + Bonus + Benefits**:If you are an agile, committed, and innovative regulatory affairs professional in the pharmaceuticals sphere, then we want to hear from you!Join us to help improve peoples’ lives and make healthcare better for everyone!**Why Pharmanovia?**:Pharmanovia is a dynamic, fast-growing...
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Regulatory Affairs Specialist
hace 1 día
Desde casa, México IQVIA A tiempo completo**Job Overview****Essential Functions**:- Acts as a Regulatory Team Leader on more complex projects, which may include technical writing;- Prepares and/or reviews regulatory documentation in area of expertise, as appropriate;- Establishes relationships with many customers; may meet face to face without rest of the team to discuss regulatory issues, present...
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Regulatory Affairs Specialist
hace 4 días
Desde casa, México ICON A tiempo completoICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...
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Regulatory Affairs Associate
hace 6 días
Desde casa, México ProductLife Group A tiempo completoIn the context of a new project, we are looking for a Regulatory Affairs Associate to join our teams in Mexico. **Responsibilities**: Assisting with the preparation of LATAM Marketing Authorization Applications Preparation and submission of documentation for post-authorization activities Compile Dossier as per country requirements Education &...
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Regulatory Affairs Associate
hace 2 días
Desde casa, México ProductLife Group A tiempo completoIn the context of a new project, we are looking for a Regulatory Affairs Associate to join our teams in Mexico.**Responsibilities**:Contribute to the regulatory activities performed. Regulatory activities include pre licensing activities, new registration (sites and medicinal products), post licensing regulatory submissions.Contribute to the production of...
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Medical Affairs Specialist
hace 4 días
Desde casa, México ICON A tiempo completoICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...