Medical Affairs Specialist

Peterborough and surrounding areas is home to Cambridgeshire, Peterborough and South Lincolnshire Mind (CPSL Mind), a values-based mental health charity working towards collaborative recovery services.About the Role:The External Affairs Specialist will join our established Communications Team, focused on promoting CPSL Mind's services and increasing income...

Job Title: Medical Affairs CoordinatorEstimated Salary: $70,000 - $100,000 per annumAbout the RoleWe are seeking a highly skilled Medical Affairs Coordinator to join our team. The successful candidate will be responsible for preparation and submission of UK MAA procedures, coordination of regulatory affairs, and maintenance of internal and external...

CK Group, a renowned science and clinical expert consultancy, is seeking a Medical Affairs Professional to join one of the world's leading innovative biopharmaceutical companies. As a key member of the team, you will work remotely on a contract basis for 6 months.Key Responsibilities:To provide medical and scientific advice to healthcare professionals and...

Bicycle Therapeutics is a clinical-stage pharmaceutical company developing innovative medicines for diseases that are underserved by existing therapeutics. As an Associate Director of Strategy, you will play a key role in helping us develop and execute medical affairs strategies and tactical plans.The estimated salary for this position is $120,000 - $160,000...

Bicycle Therapeutics is seeking an experienced Associate Director of Strategy to join our team. The estimated salary for this position is $130,000 - $170,000 per year, depending on experience and location.About the JobThis role involves developing and executing medical affairs strategies and tactical plans for assigned Bicycle assets. You will work closely...

Job SummaryVectura Group plc is seeking a highly skilled Regulatory Affairs Specialist to lead our medical device regulatory activities. This role involves assuming the role of Regulatory Affairs Manager with specialized expertise in medical devices and drug-device combination products (DDCPs). About Vectura Group plcWe are a global leader in developing...

Job SummaryWe are seeking a skilled Regulatory Affairs Specialist to join our team at Vectura Group. As a key member of our regulatory affairs department, you will play a crucial role in ensuring compliance with global regulations and guidelines for medical devices and drug-device combination products.Key Responsibilities:Lead regulatory activities across...

Job Description:The Vectura Group plc is seeking a highly skilled Regulatory Affairs Specialist to join our team. This role will be responsible for ensuring compliance with medical device regulations and directives, including the Medical Device Directive (MDD) and Medical Device Regulations (MDR).Responsibilities:Lead regulatory activities across the...

Job Title: Regulatory Affairs SpecialistEstimated Salary: $80,000 - $110,000 per annumAbout UsWe are a leading multinational pharmaceutical company based across global locations. Our mission is to accelerate access to affordable and innovative medicines.Job DescriptionThe successful candidate will be responsible for preparation and submission of UK MAA...

Regulatory Affairs Lead for Complex DevicesIndo Search is a globally ambitious company at the forefront of medical technology. We are seeking an exceptional Regulatory Affairs Lead to spearhead regulatory excellence and drive compliance for highly complex, active (electro-mechanical, software, and AI-driven) medical device technologies.Salary:...

Cambridge University Press & Assessment is a global leader in education, employing over 6,000 people worldwide. As a Global Public Affairs Specialist, you will be part of a dynamic team that maximises our impact through careful listening and collaboration to develop innovative products and services.Working closely with senior leaders, you will serve as a...

Join Sobi's Team: We are seeking an experienced Associate Medical Director, Regulatory Affairs to join our team of experts in clinical development and regulatory affairs.About the Role: The successful candidate will be responsible for leading clinical development activities, providing scientific and medical input to clinical study documents, and...

Regulatory Compliance SpecialistA renowned healthcare technology company is seeking a highly motivated Regulatory Affairs Manager to lead their regulatory compliance efforts across international markets. This individual will play a critical role in guiding the organization's innovative medical products through the regulatory approval process, ensuring...

About the Role:Newton Colmore Consulting is seeking an exceptional Medical Devices Development Specialist to join our team in Cambridge. This exciting opportunity involves working closely with our Quality Assurance and Regulatory Affairs department to develop innovative medical devices.Your Key Responsibilities:Device Development: Collaborate with our R&D...

About VCLSWe are a leading consulting firm offering expert regulatory services to the pharmaceutical and medical device sectors. Our team is dedicated to providing high-quality support to our clients, ensuring compliance with regulatory requirements.This 30-month programme is designed for recent graduates with an interest in medicines and a desire to build a...

VCLS is seeking a highly skilled Regulatory Affairs Specialist to drive forward regulatory processes, ensure compliance, and contribute to innovative clinical trials. The ideal candidate will have 4+ years of experience in Regulatory Affairs, with a focus on Clinical Trial Submissions (CTS). They will possess a deep understanding of regional and local...

Job OverviewWe are looking for a highly skilled Medical Content Specialist to join our team at Costello Medical. As a Medical Content Specialist, you will be responsible for planning and writing scientific documents, collaborating with clients, and delivering project work in a global healthcare agency.RequirementsUndergraduate degree level qualification in a...

VCLS is offering a 30-month Post-Graduate Regulatory Science Apprenticeship with TOPRA. This programme combines comprehensive Regulatory training with hands-on experience working with experienced Consultants and clients in the pharmaceutical and medical device sectors.About the ApprenticeshipThe apprenticeship is designed to provide knowledge, skills, and...

Job SummaryWe are looking for a Senior Director/Director, Medical Affairs Strategy to join our team at Vertex Ventures HC. This individual will be responsible for developing and executing medical affairs strategies, integrated evidence plans, and tactical plans for Bicycle asset(s). The ideal candidate will have prior experience in biopharmaceutical...

Job Title: Regulatory Affairs DirectorWe are seeking a highly skilled and experienced Regulatory Affairs Director to join our team at Bicycle Therapeutics. The successful candidate will be responsible for developing and executing global regulatory CMC strategy and submissions for assigned programs or projects.The ideal candidate will have extensive...