- Clinical Trial Planning: Collaborate with cross-functional teams to develop trial protocols.
- Regulatory Document Preparation: Prepare and review submission documentation ensuring accuracy completeness.
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We are seeking an experienced Senior Regulatory Affairs Associate to serve as the Portugal Local Regulatory Responsible (LRR), focusing on local regulatory requirements. · ...
Madridhace 10 horas
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We are seeking an experienced Senior Regulatory Affairs Associate to serve as the Spain Local Regulatory Responsible (LRR), focusing on local regulatory requirements and Health Authority national engagements. In this client-facing role, you will have an opportunity to work in a c ...
Madrid De jornada completahace 1 día
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We are seeking a Proposal Manager to take ownership of developing, managing, and delivering high-quality client proposals across strategic and competitive pursuits. · ...
Madridhace 3 semanas
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Job summaryVialto Partners is a market leader in global mobility services that help companies streamline and effectively manage their global mobility programs in a cost-efficient and compliant manner. · Review new RFPs or proposal requests allocated to you and break down key requ ...
Madridhace 3 semanas
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This position will be located in Spain requiring to live in Spain and have work permit. · The Job Description:Contributor to a Global Team with collective responsibility for regulatory activities associated with global pharmacovigilance including electronic pharmacovigilance syst ...
Madridhace 3 semanas
- Trabajar en empresa Trabajo a distancia
Senior Regulatory Affairs Associate
Solo para miembros registrados
We are seeking an experienced Senior Regulatory Affairs Associate to serve as the Portugal Local Regulatory Responsible (LRR), focusing on local regulatory requirements and Health Authority national engagements. · ...
Madrid, Community of Madridhace 17 horas
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We seek an experienced Senior Regulatory Affairs Associate for Spain Local Regulatory Responsible roles focusing on local regulatory requirements and national engagements. · ...
Madrid, Community of Madridhace 17 horas
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Senior Translation Project Manager coordinates and manages Regulatory Submissions for Marketing Authorization translation projects to completion. Manage multiple projects from receipt to completion. Act as main point of contact for internal/external clients and manage their requi ...
Madridhace 1 mes
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We have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan on a fully remote basis. · What you'll do: Develops and maintains knowledge of global and local regulatory requirements and industry practice/guidelines for submissio ...
Spainhace 1 mes
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The In-House Clinical Research Associate supports the Global Clinical Operations Center of Excellence conducting activities consistent with GCO's mission of building a world class shared clinical technology process innovation and clinical operations team in partnership with the c ...
Madridhace 2 semanas
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Due to our ongoing global expansion, · we have a great opportunity for a Regulatory Submissions · Specialist to join our growing regulatory team in Taiwan. · We offer a competitive salary and bonuses. · ...
Spainhace 5 días
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Global Executive Search Announcement — International Research & Innovation Talent RecruitmentSurun Talent is partnering with leading universities, laboratories, innovation centers, and high-tech enterprises in China to recruit world-class researchers, scientists , and technology ...
Madrid $100,000 - $300,000 (USD)hace 1 semana
- Trabajar en empresa
Senior Regulatory Affairs Professional- GRA EMEA HAEMATOLOGY
Solo para miembros registrados
We believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured. · Clinical Trial Applications (CTA) · Support lifecycle submissions and post-approval regulatory activities including Vari ...
Madridhace 4 semanas
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As a Study Start Up Lead at Roche you will drive and facilitate the efficient initiation of clinical trials. · ...
Madrid De jornada completahace 1 mes
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Janssen EMEA Neuroscience, Cardiovascular, Metabolic and Retina team is recruiting for an Experienced Regulatory Affairs Professional.The successful applicant will help develop and implement regulatory strategies to achieve efficient development and timely commercialization of in ...
Madridhace 1 mes
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We are seeking a highly skilled Regulatory Affairs Specialist to support our growing Spanish operation and lead EU regulatory activities. ...
Madridhace 4 semanas
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We have an exciting job opening available in our Spanish team for a Lead Accountant. You will mainly be responsible for the day-to-day accounting support functions for EMEA funds and SPVs.In this position, you will leverage your expertise in accounting to produce, analyze, and or ...
Madridhace 2 semanas
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We have an exciting job opening available in our Spanish team for a Lead Accountant. · This role involves daily accounting operations, tax compliance (including SII, VAT and coordination of CIT), and administrative support across a portfolio of Real Estate entities. ...
Madridhace 1 semana
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To provide the highest standards of quality, service delivery, and accuracy within the Operations function by reviewing instructions received from Underwriters and Underwriting Assistants. · ...
Madrid Freelancehace 3 semanas
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Vialto Partners is a market leader in global mobility services. Our purpose is to 'Connect the world'. We are unique and the only stand-alone global mobility business. · This role requires a balance of project management, persuasive writing, and collaboration with subject matter ...
Madrid, Community of Madridhace 3 semanas
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We are seeking an experienced Proposal Manager to join our team. As a key member of our bid team, you will be responsible for developing and delivering high-quality client proposals. You will work closely with leadership and experts on high-impact global opportunities. · ...
Madrid, Community of Madridhace 3 semanas
Remote Regulatory Manager — Global Submissions - Madrid - Precision Medicine Group
Descripción
As Regulatory Manager, you will oversee regulatory aspects of global submissions including preparation and review of documents. This includes ensuring high-quality data management systems to support trials.
Key Responsibilities:
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Senior Regulatory Affairs Associate
Solo para miembros registrados Madrid
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Senior Regulatory Affairs Associate
De jornada completa Solo para miembros registrados Madrid
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Proposal Manager
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Proposal Manager
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PV Medical manager- Deputy QPPV
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Senior Regulatory Affairs Associate
Solo para miembros registrados Madrid, Community of Madrid
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Senior Regulatory Affairs Associate
Solo para miembros registrados Madrid, Community of Madrid
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Senior Translation Project Manager
Solo para miembros registrados Madrid
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Regulatory Submission Specialist
Solo para miembros registrados Spain
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In‑House Clinical Research Associate, Italy
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Regulatory Submission Specialist
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Research Scientist
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Senior Regulatory Affairs Professional- GRA EMEA HAEMATOLOGY
Solo para miembros registrados Madrid
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Study Start Up Lead
De jornada completa Solo para miembros registrados Madrid
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Experienced Regulatory Affairs Professional EMEA
Solo para miembros registrados Madrid
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Regulatory Affairs Specialist
Solo para miembros registrados Madrid
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Lead Accountant
Solo para miembros registrados Madrid
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Lead Accountant
Solo para miembros registrados Madrid
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Underwriter Operations Technician
Freelance Solo para miembros registrados Madrid
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Proposal Manager
Solo para miembros registrados Madrid, Community of Madrid
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Proposal Manager
Solo para miembros registrados Madrid, Community of Madrid