Global Clinical Regulatory Expert

Job Title: Clinical Regulatory AssociateCompany Overview:TN Ireland is a global pharma company dedicated to delivering safe and effective products to patients worldwide.Job Summary:We are seeking a Clinical Regulatory Associate to join our global regulatory team and contribute to the development of our US and Canada regulatory strategies.Key...

About Us:TN Ireland is a leading global pharma company committed to delivering innovative solutions to patients worldwide.Job Summary:We are seeking a Clinical Regulatory Associate to join our global regulatory team and play a key role in shaping our US and Canada regulatory strategies.Responsibilities:Support the development of regulatory strategy by...

Job Summary:We are seeking a highly skilled Regulatory Documentation Expert to join our team at Oxford Global Resources. This is an exciting opportunity for a technical writer with expertise in creating comprehensive documents and responses tailored to regulatory requirements.The ideal candidate will have minimum 3 years of experience in technical writing...

Clinical Regulatory AssociateOur client, a global pharma company, is currently recruiting for a Clinical Regulatory Associate to join their global regulatory team on a permanent basis. As Clinical Regulatory Associate, you will be accountable for the US and Canada regulatory strategies that support the expedited delivery of safe and effective products to...

Job SummaryHibernia Services Limited is seeking a Regulatory Documentation Expert to join our team. As a Regulatory Documentation Expert, you will be responsible for developing and finalizing high-quality clinical trial documents, including study protocols, protocol amendments, investigator brochures, and clinical study reports.You will work closely with...

We are seeking a highly skilled and experienced Global Clinical Trials Lead to join our team at Eli Lilly and Company. As a Global Clinical Trials Lead, you will be responsible for developing and executing clinical trials across various regions and countries.You will work closely with cross-functional teams to develop and implement trial strategies, manage...

Hobson Prior's Global Regulatory Compliance Manager will oversee the development of Chemistry, Manufacturing and Controls processes. This critical role will ensure compliance with regulatory requirements and provide strategic guidance for worldwide clinical trials, market registration submissions, and post-approval submissions.The ideal candidate will have...

Key ResponsibilitiesDevelop deep technical knowledge of CMC drug development science(s).Demonstrate knowledge of global CMC regulatory requirements and guidelines for conducting clinical trials and product registrations.Assist in the development of regulatory strategy and update strategy based upon global regulatory changes.Provide high-quality and timely...

Job OverviewThe Compendial Compliance Specialist position sits within the Physico-chemical Sciences and Sample Management team as part of the wider BTDS AD Department.As a Regulatory Compliance Expert, you will act as a Large Molecule, Subject Matter Expert (SME) solely responsible for ownership of compendial and particulates methods.Your primary focus will...

Job DescriptionWe are seeking a highly experienced Medical Writer and Regulatory Expert to join our team at Hibernia Services Limited. As a key member of our regulatory affairs department, you will be responsible for creating high-quality clinical trial documents that meet the highest standards of scientific integrity.About the RoleYou will develop...

Eli Lilly And Company is a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.We give our best effort to our work,...

Job Summary:The Regulatory Lead for Global Labeling will play a critical role in ensuring the development and maintenance of global labeling, including all core labeling documents related to drug, device, CMC, and carton/container components.This position is responsible for leading the development and implementation of global labeling strategy to facilitate...

Job Summary:We are seeking a Medical Writer to join our team in Cork/Dublin. The successful candidate will have experience in medical writing within the clinical research industry, with a focus on Phase 1 and Phase 2 clinical trials.Responsibilities:Document Development:Develop high-quality clinical trial documents, including study protocols, initial...

About the RoleThe Clinical Trials Documentation Lead will be responsible for overseeing the development and submission of clinical trial documents to regulatory authorities. This role requires a deep understanding of clinical research methodologies, regulatory requirements, and medical writing principles. The ideal candidate will have a proven track record...

Eli Lilly and Company's mission is to provide innovative solutions for patients worldwide. As a Global Clinical Regulatory Associate, you will play a crucial role in ensuring the delivery of safe and effective products to patients. You will be responsible for leading the registration management process, providing expertise in electronic submission...

Job DescriptionWe are seeking an experienced Associate Director Global Regulatory Affairs to join our team. As a key member of our regulatory affairs department, you will be responsible for leading and managing global regulatory affairs teams, ensuring compliance with regulatory requirements and providing strategic guidance to stakeholders.Company...

Eli Lilly and Company is a global healthcare leader with a rich history of innovation and discovery. Our mission is to unite caring with discovery to make life better for people around the world. We are committed to developing innovative solutions that improve patient outcomes and enhance the understanding and management of disease.As a Clinical...

At Eli Lilly and Company, we unite innovation with excellence to make life better for people around the world. Our global healthcare leader is headquartered in Indianapolis, Indiana. Our employees work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

Company OverviewMMS is a leading clinical research organization (CRO) that prioritizes innovation and employee satisfaction. Our award-winning data-focused approach sets us apart in the industry.We strive to maintain a collaborative and inclusive work environment, fostering exceptional culture and industry-leading employee retention rates.Our global presence...

About the RoleWe are looking for a highly skilled Medical Writing Expert to join our team at evo talent. As a key member of our clinical operations group, you will be responsible for the development and management of high-quality clinical trial documents.The ideal candidate will have a strong background in medical writing and experience working on Phase 1...