Regulatory Submissions Project Manager

Job SummaryWe are seeking a highly skilled Regulatory Affairs Manager to join our team. As a key member of our regulatory team, you will be responsible for managing the preparation and revision of labeling and regulatory submissions for our pharmaceutical products.Key Responsibilities:Manage the creation and maintenance of labeling and regulatory...

Job SummaryThe Junior Manager, Regulatory Affairs CMC is responsible for providing regulatory technical assistance to development teams and ensuring the adequacy of CMC documentation for global regulatory submissions. This includes specific requirements for regional registration processes. The position supports and promotes all regulatory CMC tasks...

Job Summary:The Junior Manager, Regulatory Affairs CMC is responsible for providing regulatory relevant technical assistance to development teams and ensuring the adequacy of CMC documentation for global regulatory submissions, including specific requirements for regional registration processes. This position supports and promotes all regulatory CMC tasks...

Job Title:Senior Regulatory Affairs Manager - Medical Device/Post-Job Summary:Cpl Healthcare is seeking a Senior Regulatory Affairs Manager to join our team in Spain, Madrid. As a Senior Regulatory Affairs Manager, you will be responsible for the strategic lifecycle management of our medical device portfolio, including post-CE approval and operational...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Montezuma Winery Llc. As a key member of our regulatory team, you will be responsible for ensuring compliance with global pharmaceutical regulations and managing the creation and maintenance of labelling documentation.Key ResponsibilitiesParticipate in the...

Job Title: Associate Director, Regulatory Affairs Medical Devices Lifecycle ManagementJob Type: Full Time, Permanent PositionLocations: Spain, Madrid – HybridRemuneration: Attractive salary and packageCpl Healthcare is seeking an experienced Associate Director, Regulatory Affairs Medical Devices Lifecycle Management to join our team. As a key member of our...

Job Title: Associate Director, Regulatory Affairs - Medical Device/Post-Market SurveillanceJob Type: Full Time, Permanent PositionLocations: Spain, Madrid – HybridRemuneration: Attractive salary and packageAn exciting opportunity to join a growing pharmaceutical company that specializes in Cancer and Supportive Care, Gastroenterology and Hepatology. Due to...

At PC Recruiter, we are seeking a Regulatory Administration Specialist to support the implementation of our regulatory strategy and ensure compliance with all requirements. Key Responsibilities: Support the growth and maintenance of our CP portfolio in the South Cluster, ensuring timely regulatory submissions and administration. Assist in the preparation and...

As a seasoned project manager, you will oversee the execution of complex construction projects in our Spanish Datacenter. Your key responsibilities will include:Key ResponsibilitiesLeading the project team to ensure timely completion and within budgetCoordinating with our French specialist teams to design and deliver high-quality projectsManaging...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Montezuma Winery Llc. This is a challenging opportunity for a professional with experience in labeling activities for innovator drugs on a global level.Key ResponsibilitiesParticipate in the preparation and revision of informative texts for healthcare professionals...

Regulatory Affairs ManagerWe are seeking a highly skilled Regulatory Affairs Manager to join our team at Montezuma Winery Llc. As a key member of our regulatory team, you will be responsible for ensuring compliance with global pharmaceutical regulations and managing the creation and maintenance of labelling documentation.Key Responsibilities:Participate in...

Regulatory and Start-Up SpecialistPrecision Medicine Group is a unique Contract Research Organization (CRO) that combines cutting-edge technologies, expertise, and operational scale to accelerate the development of life-changing therapies. We are seeking a highly skilled Regulatory and Start-Up Specialist to join our team in Spain, working fully remotely....

We are seeking an experienced Localization Project Coordinator to lead and/or support relationship building and project delivery for clients operating in the regulated industries and governmental space.This role will involve managing the full lifecycle of translation projects from inception to completion, determining resource requirements, and ensuring...

Job SummaryWe are seeking a highly skilled Regulatory Coordinator - Site Start-Up Specialist to join our team at Pharmiweb. As a key member of our site start-up team, you will be responsible for ensuring the smooth execution of clinical trials at investigative sites. Your primary focus will be on providing support with site selection, contract management,...

Job SummaryAs a Wind Project Manager at Qenergy, you will play a crucial role in driving the success of our portfolio projects. You will oversee the grid connection process and administrative milestones, ensuring smooth progress across all stages. Your expertise will help identify and mitigate risks or delays related to evacuation infrastructure.Key...

Job Title: Clinical Project Manager - Global StudiesWe are seeking a highly skilled Clinical Project Manager to lead our global studies team. As a key member of our team, you will be responsible for managing projects from start to finish, ensuring compliance with GCP, SOPs, and regulatory requirements.Key Responsibilities:* Manage projects as a project...

About the RoleThe Clinical Research Associate (CRA) supports the Global Clinical Operations (GCO) Centre 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 company's divisions, through technology enablement,...

Regulatory Strategy and ComplianceBitfinex, a leading digital asset trading platform, is seeking a highly skilled Regulatory Compliance Specialist to join its Regulatory and Licensing team. The successful candidate will have a deep understanding of legal and regulatory requirements in the Middle East / North Africa region and will be responsible for...

Job SummaryThe Clinical Trials Project Manager will be responsible for managing a portfolio of clinical trials within ICON Medical Imaging and Cardiac Safety Solutions team. This role will act as the primary point of contact for customer communication, managing routine teleconferences and reporting deliverables. The Project Manager will develop project...

Unlock Your Potential in Medical WritingWe are seeking a highly skilled and experienced Senior Medical Editor - Global Regulatory Compliance Specialist to join our team at Pharmiweb.About the RoleThis is a unique opportunity for a medical writing expert with a passion for regulatory compliance to take on a challenging role that requires strong technical...