Regulatory Affairs Manager | Clinical Development
1 giorno fa
Regulatory Affairs Manager | Clinical Development (CTA/IND) | EU/US/RoW ABOUT / INFO Regulatory Affairs professional with 7 - 10 years of experience in the pharmaceutical industry, supporting global clinical development programs across EU, US and RoW. Strong track record in managing clinical trial applications and maintenance activities (CTA/IND), coordinating complex submission packages, and ensuring compliance with international regulatory requirements (ICH/GCP). Experienced in regulatory strategy and execution, including formal meeting with major Regulatory Agencies. Experienced in the submission of ODD, PIP, NDA/BLA and MAA. Used to working in cross-functional environments, partnering closely with Clinical Operations, CMC, Pharmacovigilance, and external CROs to deliver high-quality dossiers within tight timelines. Key strengths include regulatory intelligence, critical thinking, structured problem-solving, and the ability to translate complex regulatory expectations into actionable project plans. Passionate about scientific innovation and contributing to projects addressing orphan drugs and unmet medical needs. Areas of expertise Global CTA/IND/IMPD submissions and maintenance MAA/NDA/BLA submissions EU/US/RoW regulatory requirements for medicines licenses Authority liaison and response management DSUR / Annual Safety Reporting support and PV interface Cross-functional coordination High-quality document preparation and submission planning Keywords / Skills Regulatory Affairs (Clinical Development) CTA / IND / IMPD submissions MAA / NDA / BLA EU CTR / Clinical Trial Regulation Competent Authorities interactions Regulatory strategy Substantial amendments DSUR / ASR SUSAR reporting (oversight/coordination) ICH / GCP compliance Clinical trial documentation (Protocol, IB, ICF, responses) Regulatory intelligence / guidelines monitoring ODD / UMN therapeutic areas Target roles Regulatory Affairs R&D Manager Areas Pharma / Biotech Are you interested? Are you interested? Send your application or contact us directly for a confidential conversation. Option One Life Science Consulting – Connecting Compliance & Business #J-18808-Ljbffr
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Regulatory Affairs Lead – Clinical Development
1 giorno fa
Turbigo, Italia Option One Life Science Consulting Sagl A tempo pienoA leading life science consulting firm is seeking a Regulatory Affairs Manager to support global clinical development programs. The ideal candidate will have 7-10 years of experience in the pharmaceutical industry, with a strong background in managing clinical trial applications, including CTA/IND submissions and compliance with regulatory requirements...
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Medical Affairs Manager
1 giorno fa
Turbigo, Italia Johnson & Johnson Innovative Medicine A tempo pienoOverview All Job Posting Locations: Milano, Italy In Johnson & Johnson crediamo che la salute sia tutto. Il nostro impegno nell’innovazione sanitaria ci consente di costruire un mondo in cui le malattie complesse vengono prevenute, trattate e curate, in cui i trattamenti sono più intelligenti e meno invasivi e le soluzioni sono personalizzate. At Johnson...
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Medical Affairs Manager
1 giorno fa
Turbigo, Italia Johnson & Johnson Innovative Medicine A tempo pienoOverview All Job Posting Locations: Milano, Italy In Johnson & Johnson crediamo che la salute sia tutto. Il nostro impegno nell’innovazione sanitaria ci consente di costruire un mondo in cui le malattie complesse vengono prevenute, trattate e curate, in cui i trattamenti sono più intelligenti e meno invasivi e le soluzioni sono personalizzate. At Johnson...
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Clinical Project Lead
6 giorni fa
Turbigo, Italia Barrington James A tempo pienoClinical Project Manager – Neuro / Psychiatry Location Department Clinical Operations Reports to Senior Clinical Project Manager / Director of Clinical Operations Job Purpose The Clinical Project Manager (CPM) is responsible for the planning, execution, and delivery of clinical trials within Neurology and Psychiatry, ensuring studies are conducted on time,...
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Clinical Project Lead
6 giorni fa
Turbigo, Italia Barrington James A tempo pienoClinical Project Manager – Neuro / Psychiatry Location Department Clinical Operations Reports to Senior Clinical Project Manager / Director of Clinical Operations Job Purpose The Clinical Project Manager (CPM) is responsible for the planning, execution, and delivery of clinical trials within Neurology and Psychiatry, ensuring studies are conducted on time,...
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Sr. Clinical Trial Manager
2 settimane fa
Turbigo, Italia Syneos Health A tempo pienoSr. Clinical Trial Manager (Clinical Research Medical Advisor) – FSP – Homebased – ItalyJoin to apply for the Sr. Clinical Trial Manager (Clinical Research Medical Advisor) – FSP – Homebased – Italy role at Syneos Health.Company OverviewSyneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate...
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Sr. Clinical Trial Manager
2 settimane fa
turbigo, Italia Syneos Health A tempo pienoSr. Clinical Trial Manager (Clinical Research Medical Advisor) – FSP – Homebased – ItalyJoin to apply for the Sr. Clinical Trial Manager (Clinical Research Medical Advisor) – FSP – Homebased – Italy role at Syneos Health.Company OverviewSyneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate...
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Sr. Clinical Trial Manager
2 settimane fa
Turbigo, Italia Syneos Health A tempo pienoSr. Clinical Trial Manager (Clinical Research Medical Advisor) – FSP – Homebased – Italy Join to apply for the Sr. Clinical Trial Manager (Clinical Research Medical Advisor) – FSP – Homebased – Italy role at Syneos Health. Company Overview Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate...
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Senior Clinical Trial Manager – Remote
2 settimane fa
Turbigo, Italia Syneos Health A tempo pienoA global biopharmaceutical organization is looking for a Sr. Clinical Trial Manager to ensure the execution of clinical trials in Italy. This role requires providing medical and scientific leadership, auditing regulatory compliance, and collaborating with cross-functional teams. Candidates should have a Medical Doctor degree or a related Pharma degree and at...
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Global Regulatory Affairs Specialist
2 settimane fa
Turbigo, Italia Alfasigma A tempo pienoA global healthcare company based in Italy is seeking a Non-Pharma Global Regulatory Affairs Specialist with at least 5 years of experience in regulatory affairs, especially in food supplements and medical devices. The role involves managing regulatory documentation for projects across EU and global markets, collaborating with various teams to ensure...