Regulatory Affairs Director for Clinical Trials

Role OverviewWe are seeking an experienced Clinical Trials Specialist to join our team at Worldwide Clinical Trials, a leading global contract research organization.About the RoleThe successful candidate will be responsible for overseeing the execution of clinical trials in accordance with regulatory requirements and industry standards.Key...

Job SummaryWe are seeking a highly skilled Clinical Trials Director to lead our global clinical trials team. As a key member of our organization, you will be responsible for developing and implementing trial site feasibility support and potential referral sites specific strategies. Your expertise in clinical research, patient recruitment, and...

Job Summary:The Senior Director of Clinical Affairs, EMEA RM will lead a dynamic team responsible for professional education, Investigator-Sponsored Research (ISR), and collaborative trials within the EMEA region. This role requires a strategic leader with a deep understanding of clinical affairs and a proven track record in managing high-performing...

About the RoleWe are seeking a highly skilled Regulatory Affairs Associate Director to join our CMC team in Barcelona, Spain.Key Responsibilities* Provide strategic, tactical, and operational expertise to project teams* Develop creative strategies to support new biological entities and novel products* Collaborate with cross-functional teams to ensure...

Job SummaryThe Senior Manager, Regulatory Affairs will lead the regional regulatory affairs department to ensure compliance with Innovaderm's standard operating procedures, applicable regulations, and good clinical practices. Key responsibilities include providing strategic guidance on regulatory activities, overseeing the performance of direct reports, and...

Unlock Your Potential as a Clinical Trials DirectorAs a Clinical Trials Director at Syneos Health, you will lead a team of Research Science Liaisons globally, focusing on patient identification, enrollment, and retention in clinical trials. Your expertise in developing and implementing trial site feasibility support and potential referral sites specific...

Job Summary:The Senior Director of Clinical Affairs, EMEA RM, will be responsible for leading a dynamic team dedicated to professional education, Investigator-Sponsored Research (ISR), and collaborative trials within the EMEA region.This role requires a strategic leader with a deep understanding of clinical affairs and a proven track record in managing...

Job Title: CMC Regulatory Affairs Associate DirectorAbout the Role: We are seeking a highly skilled CMC Regulatory Affairs Associate Director to join our dynamic team in Barcelona, Spain. As a key member of our cross-functional Regulatory Strategy, Pharmaceutical, and Global Supply Teams, you will collaborate with colleagues across the globe to ensure...

Job Title: Regulatory Affairs SpecialistGalderma is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will be responsible for delivering innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities.Develop and manage clinical trial regulatory...

Our Mission and ApproachAt Worldwide Clinical Trials, we're dedicated to advancing clinical research and improving lives. We take a pioneering and creative approach to our work, pushing boundaries and innovating to make a difference.About the RoleWe're seeking a Clinical Research Associate to join our team. As a CRA, you'll work alongside brilliant minds...

The Senior Manager, Regulatory Affairs will lead the regional regulatory affairs department at Innovaderm Research, ensuring all services are conducted according to standard operating procedures, applicable regulations, and good clinical practices. Key responsibilities include providing leadership on regulatory activities, planning and assigning work,...

**About ICON**ICON plc is a leading healthcare intelligence and clinical research organization. We pride ourselves on fostering an inclusive environment that drives innovation and excellence, and we welcome you to be part of our mission to shape the future of clinical development.**Job Description**We are currently seeking a Clinical Research Coordinator -...

Job Description:">The Regulatory Affairs Strategist is responsible for delivering innovative global regulatory strategies for clinical trial registration with health authorities. This role oversees the regulatory aspects related to clinical trial submissions, aligning with the company's global business strategy and partnering with subject matter experts...

Job Title: Regulatory Affairs SpecialistAt Galderma, we are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will be responsible for delivering innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities. You will work closely with our global...

Lead Clinical Trials to SuccessAs a Clinical Trials Director at Syneos Health Commercial Solutions, you will lead a team of Research Science Liaisons to drive patient enrollment and retention in clinical trials. Your strategic thinking and leadership skills will empower your team to provide clinical expertise to healthcare providers, improving patient...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Galderma. As a Regulatory Affairs Specialist, you will be responsible for delivering innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities.Key ResponsibilitiesCreating and managing clinical trial regulatory...

Medical Director for Clinical TrialsAt Thermo Fisher Scientific, we are seeking a highly skilled Medical Director to provide medical support and advice for clinical trials within the Pharmacovigilance department.About the RoleThe successful candidate will be responsible for providing medical leadership to study teams, including creating clinical trial...

Job Summary: We are seeking a highly skilled Clinical Trials Coordinator to join our team at Creal. The successful candidate will be responsible for developing and maintaining Standard Operating Procedures (SOPs) for clinical trials, ensuring compliance with regulatory requirements and best practices. Key Responsibilities:Develop and maintain SOPs for...

Job SummaryThe Regulatory Affairs Associate will be responsible for delivering innovative global regulatory strategies for clinical trial registration with health authorities. This role will oversee regulatory aspects related to clinical trial submissions, ensuring accurate and compliant dossiers.Key ResponsibilitiesDevelop and execute clinical trial...

Job DescriptionISGlobal is seeking a highly skilled Clinical Trials Coordinator to join our team. The successful candidate will be responsible for developing and maintaining Standard Operating Procedures (SOPs) for clinical trials, ensuring compliance with regulatory requirements and promoting quality management throughout the research process.The ideal...