Regulatory Writer and Project Manager

**Job Opportunity**We are seeking a highly skilled Senior Medical Writer Oncology to join our dynamic team at Gilead. As a senior-level medical writer, you will be responsible for authoring complex regulatory documents, leading review and planning processes, and representing Medical Writing on cross-functional teams.With significant experience in the...

Job DescriptionVCLS is a renowned company in the pharmaceutical industry, seeking an experienced Senior Medical Writer to join its team. As a key member of the VCLS team, you will be responsible for creating high-quality medical documents for various client projects.Key Responsibilities:Lead authoring of clinical and regulatory documents, including study...

Gilead Sciences is a global biopharmaceutical company that is committed to making a difference in the lives of people with life-threatening diseases. We are seeking a highly skilled Senior Medical Writer to join our dynamic team. As a Senior Medical Writer, you will be responsible for authoring complex regulatory documents, including clinical study reports,...

Job OverviewWe are seeking a highly skilled Regulatory Document Specialist to join our team at VCLS. As a key member of the team, you will be responsible for creating high-quality medical documents for various client projects.The ideal candidate will have a strong background in regulatory affairs and excellent writing skills. You will work closely with...

Vivify Talent Overview:We're a small yet ambitious regulatory writing consultancy looking for a talented Principal Medical Writer to drive our projects forward. With a focus on flexibility and work-life balance, we offer a unique opportunity to excel in a fully remote role.As a key member of our team, you'll be responsible for leading the creation of...

At Outlier, we're looking for a talented Content Writer to help us improve our AI models. With your expertise in German, you'll be responsible for training generative artificial intelligence models by reviewing and rating text responses.About the OpportunityThis freelance opportunity allows you to work remotely with flexible hours, making it perfect for...

Job Title: Content Writer for AI TrainingWe're seeking a skilled writer to help train AI models for innovative companies worldwide. This freelance opportunity offers flexibility, allowing you to work remotely and at hours that suit you best.About the Opportunity:We're looking for talented writers with fluency in German to assist in training generative...

Join Our TeamWe are seeking a highly skilled Documentation and Standards Writer to join our team. As a Graduate Technical Writer, you will be responsible for creating and maintaining high-quality technical content and user documentation.This is an exciting opportunity to work with a diverse group of professionals who bring a rich mix of technical and...

**Job Overview**We are seeking a highly skilled Medical Writing Senior Manager to join our dynamic team at Gilead. As a senior-level medical writer, you will be responsible for authoring complex regulatory documents, leading review and planning processes, and representing Medical Writing on cross-functional teams.With significant experience in the biopharma...

About GileadGilead Sciences, Inc. is a global biopharmaceutical company dedicated to developing innovative treatments for life-threatening diseases. We're looking for talented individuals to join our team as Regulatory Affairs Manager.Job DescriptionThis role will act as the Regional Regulatory Lead on complex or multiple products, compounds, indications or...

Job Overview">We are seeking experienced Dutch writers to help train generative artificial intelligence models at Outlier AI. As a freelancer, you will work remotely and have flexible hours.">Key Responsibilities">">Read and rank Dutch text produced by an AI model">Write short stories in Dutch about given topics">Evaluate the factual accuracy of Dutch text...

Job OverviewWe are seeking experienced writers with fluency in French to help train generative artificial intelligence models.This freelance opportunity is remote and hours are flexible, so you can work whenever is best for you.Your expertise will be utilized in the following ways:You will read French text to rank a series of responses produced by an AI...

At Gilead Sciences, Inc., we're seeking a highly experienced Regulatory Affairs Manager to lead our Global Regulatory team in the development and implementation of regulatory strategies for our Therapeutic Area (TA) portfolio. This role will oversee the preparation and submission of regulatory documents, as well as ensure compliance with global...

Senior Medical Writing PositionWe are partnering with AL Solutions to find a highly skilled Senior Manager of Medical Writing. This key role involves creating high-quality regulatory documents and working closely with cross-functional teams to drive project success.About the OpportunityThe successful candidate will have extensive experience in medical...

Job DescriptionWe are seeking an experienced Global Regulatory Affairs Manager to join our team. This role will be responsible for leading the development and implementation of global regulatory strategies for multiple products or projects. The ideal candidate will have a strong background in regulatory affairs, excellent leadership skills, and the ability...

MoonLake Immunotherapeutics is an exciting place to work, offering a unique opportunity to contribute to ground-breaking projects that have the potential to transform global healthcare. As a Global Regulatory Strategy Manager, you will play a key role in developing and implementing innovative regulatory strategies for sonelokimab lead indication(s).About the...

About the RoleWe are seeking a Senior Manager of Medical Writing to join our team at AL Solutions. As a key member of our regulatory content team, you will be responsible for creating high-quality documents that meet regulatory requirements.Your primary focus will be on producing regulatory documents, facilitating the review and editing process, and...

**Key Responsibilities** The key responsibilities of this role include:Creating and maintaining user documentation and other technical contentParticipating in documentation projects, taking a leading or supporting role based on project sizeEnsuring content meets the needs of end users, is precise, and adheres to ARM's writing standardsCollaborating with...

About the RoleThis is an exciting opportunity to join Gilead Sciences, Inc. as a Regulatory Affairs Manager within the Virology Franchise. You will be responsible for developing and executing regulatory strategies for designated products, preparing and maintaining regulatory submissions, and partnering with cross-functional teams.ResponsibilitiesManage and...

Job OverviewVivify Talent Limited is seeking an experienced Regulatory Content Lead to spearhead the development of critical regulatory documents and contribute to project strategy and planning.The ideal candidate will have a strong understanding of science and regulatory principles, excellent communication and project management skills, and proven...