Expert Medical Regulatory Content Specialist

Job Title: Regulatory Medical Writer SpecialistJob Type: Full-timeSalary: $120,000 - $150,000 per yearLocation: Hyderabad, Telangana, IndiaAbout Company: Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT.About Job: We are seeking an experienced Regulatory Medical Writer Specialist to join our team. As a key member of our medical writing...

Job Title: Regulatory Affairs Expert for Medical DevicesLocation: Hyderabad, Telangana, IndiaSalary: ₹2,100,000 per annum (based on industry standards)About the Job:Lifelancer is a leading talent-hiring platform in Life Sciences, Pharma, and IT. We connect talented professionals with opportunities in pharma, biotech, health sciences, healthtech, and IT...

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...

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,...

About the Role:We are seeking a skilled Content Writer to join our team as a Specialist for Regulatory Documentation at Vimta Labs Ltd in Hyderabad, Telangana, India.Job Overview:This is a full-time mid-senior level position that requires experience in protocol design, clinical trial management, and regulatory submission.Key Responsibilities:Design and...

About the JobAs a Medical Regulatory Writer with our team at Sanofi Global Hub, you will play a crucial role in creating high-quality safety and clinical documents that meet regulatory requirements.ResponsibilitiesDevelop and edit medical sections of Periodic Benefit-Risk Evaluation Reports, Clinical Study Reports, and other critical documents.Collaborate...

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 the Job">We are seeking a highly skilled Regulatory Writer Expert to join our team at Sanofi Global Hub in Hyderabad, India.">As a key member of our medical writing team, you will be responsible for creating high-quality safety and clinical documents, including Periodic Benefit-Risk Evaluation Reports, Clinical Study Reports, and product alerts.">Your...

Job OverviewWe are seeking an experienced Medical Regulatory Writer to join our team at Lifelancer, a leading talent-hiring platform in Life Sciences, Pharma and IT. The successful candidate will be responsible for creating high-quality clinical and safety documents for submission to regulatory authorities.About the RoleWrite and/or edit complex Clinical...

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 UsLifelancer is a talent-hiring platform connecting professionals with opportunities in the life sciences, pharma, and IT domains.Job DescriptionWe are seeking a highly skilled Medical Regulatory Writer to join our Global Hub team. As a Senior Medical Regulatory Writer, you will be responsible for writing and/or editing high-quality safety and clinical...

Job OverviewIn this role, you will work as a Senior Regulatory Writer creating high-quality medical documents for the pharmaceutical industry. The ideal candidate has 5+ years of experience in regulatory writing and is proficient in English.

We are seeking a highly skilled Regulatory Medical Writer to lead our medical writing team at Lifelancer.Job OverviewThis is an exciting opportunity for a seasoned medical writer to join our dynamic team and contribute to the development of high-quality medical documents. As a key member of our regulatory affairs team, you will be responsible for creating...

Medtronic is a global healthcare technology leader that empowers innovators to boldly attack the most challenging health problems. We're committed to alleviating pain, restoring health, and extending life through cutting-edge solutions.">Job Overview: As a Senior Regulatory Affairs Specialist at Medtronic, you'll play a crucial role in ensuring compliance...

About Lifelancer">Lifelancer is a leading talent-hiring platform in Life Sciences, Pharma and IT, connecting professionals with exciting opportunities in pharma, biotech, health sciences, healthtech and IT domains.Competitive Salary: $100,000 - $150,000 per yearThe ideal candidate will have a strong background in Regulatory Affairs, with experience in the...

Job Title: Pharmaceutical Regulatory Content WriterSalary: ₹ 1,500,000 per year (estimated)About the JobWe are seeking an experienced Pharmaceutical Regulatory Content Writer to join our team at Lifelancer. As a key member of our organization, you will be responsible for writing and editing high-quality safety and clinical documents, medical sections of...

OverviewLifelancer is a dynamic platform connecting talented professionals with opportunities in life sciences, pharma, and IT. We're seeking an exceptional Regulatory Affairs Specialist II to join our team.Job DescriptionThis role will focus on supporting the launch of new products, ensuring regulatory compliance across global markets. Key responsibilities...

About the RoleWe are seeking a highly skilled Medical Documentation and Quality Assurance Specialist to join our team at Lifelancer. In this role, you will be responsible for ensuring the accuracy and quality of medical documentation, as well as collaborating with cross-functional teams to implement quality assurance processes.Job ResponsibilitiesDevelop and...

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...

About the RoleAs a Global Regulatory Writing Expert at Lifelancer, you will play a crucial role in authoring and gaining approval of scientific and regulatory submission documents that comply with global regulatory standards.Maintaining key business relationships with cross-functional product team members is essential for success in this position. This role...