Regulatory Medical Writer Lead

Company OverviewSanofi Global Hub is a strategic partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally.About the JobWe are seeking a skilled Regulatory Writer to create high-quality medical content for our clients in the pharmaceutical industry.Your primary responsibility will be to develop and maintain TA...

Job OverviewLifelancer is a talent-hiring platform that connects professionals with opportunities in Life Sciences, Pharma, and IT. As a Senior Medical Regulatory Writer, you will be part of our team supporting the pharmaceutical industry.About the RoleWe are seeking an experienced Medical Regulatory Writer to join our team. The ideal candidate will have 5...

About the RoleJoin a team of professionals dedicated to creating high-quality medical content for the pharmaceutical industry.Job DescriptionWe are seeking an experienced Senior Regulatory Medical Writer to join our team. As a key member of our writing team, you will be responsible for developing and editing clinical and safety documents for submission to...

About the CompanyLifelancer is a leading talent-hiring platform specializing in Life Sciences, Pharma, and IT. We connect exceptional professionals with opportunities in pharmaceuticals, biotechnology, health sciences, healthtech, and IT domains.Job Title and DescriptionThe ideal candidate will hold a senior position as a Regulatory Medical Writer, focusing...

Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. We connect talented professionals with opportunities in pharma, biotech, health sciences, healthtech and IT domains.About ProPharma GroupFor the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device,...

At Lifelancer, we're on a mission to connect talented professionals with exciting opportunities in life sciences and pharmaceuticals. We're currently seeking a highly skilled regulatory writer to join our team.As a regulatory writer, you'll play a crucial role in creating high-quality clinical and safety documents for submission to regulatory authorities....

About the Role: We are seeking a seasoned Regulatory Medical Writing Manager with expertise in Immunology to join our team at Lifelancer. This is a rare opportunity to work on cutting-edge medical solutions that address complex diseases and improve people's lives. The successful candidate will lead a team of medical writers, manage projects, and oversee the...

Job Overview: We are seeking an experienced Pharmaceutical Regulatory Writer to join our team at Lifelancer. As a key member of our global organization, you will be responsible for creating high-quality clinical and safety documents for submission to regulatory authorities.About the Role: In this role, you will work independently on complex documents, acting...

Company OverviewLifelancer is a talent-hiring platform that connects professionals with opportunities in life sciences, pharma, and IT. Our mission is to empower individuals to succeed in their careers.About the RoleWe are seeking an experienced medical writer to join our team. As a Senior Medical Writer II, you will be responsible for authoring high-quality...

About the OpportunityWe are seeking an experienced Global Medical Expert to join our team at Lifelancer in a regulatory lead role. This is a fantastic opportunity for someone with a strong background in medical affairs, clinical development, and pharmacovigilance.Job DescriptionProvide medical assessment with relevant and updated clinical evidence to support...

About this RoleWe are seeking a highly skilled Senior Regulatory Content Expert to join our team at Lifelancer. In this role, you will be responsible for creating and editing high-quality clinical and safety documents for submission to regulatory authorities.Key Responsibilities:Write and/or edit complex Clinical Study Reports (CSR), CTD submission...

Company Overview:Lifelancer is a talent-hiring platform that connects professionals with opportunities in life sciences, pharma, and IT.About the Job:We are seeking a highly skilled Regulatory Content Specialist to join our team. As a Regulatory Content Specialist, you will be responsible for creating high-quality safety and clinical documents, medical...

About Lifelancer, a leading talent-hiring platform in Life Sciences, Pharma and IT.Job OverviewLifelancer is seeking an experienced Senior Regulatory Affairs Specialist- Q&R to join our team. This role will be responsible for ensuring compliance with regulatory requirements and providing strategic support for global product submissions.Key...

Job OverviewWe are seeking a highly skilled Regulatory Affairs Specialist II to join our team in Hyderabad, India. As a key member of our regulatory affairs function, you will play a crucial role in ensuring compliance with Indian and international regulations for research and development activities.About the RoleThe successful candidate will have a strong...

About MedtronicCareers that Change LivesMedtronic is a global leader in healthcare technology. As a Regulatory Compliance Manager, you will play a critical role in ensuring the quality and safety of our medical devices.

Job OverviewWe are seeking a skilled Regulatory Affairs Specialist to join our team in Hyderabad, India. This role will be responsible for ensuring compliance with Indian and international regulations, collaborating with cross-functional teams, and supporting the development of medical devices.

About the RoleAs a Medical Coding Specialist at Bristol Myers Squibb, you will play a vital role in ensuring compliance with global regulatory requirements for single case safety reporting.The successful candidate will join our Worldwide Patient Safety team, supporting the vision of transforming patients' lives through science.This is a dynamic and...

Job Title: Director of Research & Development IndiaCompany: Olympus Medical Systems India Pvt LtdAbout Us:Olympus Medical Systems India Pvt Ltd is a leading company in the medical devices industry. We are looking for a highly skilled and experienced Director of Research & Development India to join our team.Job Summary:We are seeking a talented and motivated...

About the JobWe are seeking a highly skilled Senior Regulatory Affairs Specialist- Q&R to join our team at Lifelancer, a leading talent-hiring platform in Life Sciences, Pharma, and IT. As a key member of our regulatory affairs function, you will play a critical role in ensuring compliance with global regulations and maintaining the highest standards of...

Bristol Myers Squibb is a global biopharmaceutical leader that delivers innovative, life-changing medicines for patients.About the RoleAs a Senior Manager, Global Submission Management, Clinical Trials, you will be responsible for managing and coordinating the timely, compliant, and accurate delivery of core submission documents and dossiers to BMS HA/EC...