Medical Writing and Clinical Disclosure Professional

Job DescriptionKey ResponsibilitiesPlan, Handle, Manage, Structure, and Write Clear Regulatory Documents: As a Medical Writing and Clinical Disclosure Professional, your objective will be to plan, handle, manage, structure, and write clear, concise, and audience-friendly regulatory, scientific, and medical documents fit for purpose.Lead Cross-Functional...

About the RoleWe are seeking a highly skilled Clinical Trial Disclosure Specialist to join our team at Genmab. In this role, you will play a crucial part in executing global and national clinical trial disclosure requirements across our entire portfolio.Key ResponsibilitiesManage and track public disclosure of clinical trial protocols, results, and document...

Job OverviewPharma IT is seeking an experienced Senior/Principal Medical Writing Consultants to join our Regulatory Affairs & Medical Writing Team. In this role, you will work as a consultant to support our clients in the Pharma, Biotech and Medical Device industries.This position offers an exciting opportunity for a highly skilled medical writer to take on...

Job OverviewPharma IT is seeking a seasoned Senior/Principal Medical Writing Consultant to join our Regulatory Affairs & Medical Writing Team.The ideal candidate will have extensive experience in medical writing, with a strong understanding of international regulations and ICH guidelines.You will work as a consultant to support clients in the Pharma,...

Senior/Principal Medical Writing ConsultantsPharma IT is hiring experienced Senior/Principal Medical Writer Consultants to join our Regulatory Affairs & Medical Writing TeamIn this role, you will work as a consultant to support our clients in the Pharma, Biotech and Medical Device industries.In this position, you will work on-site at the client's location or...

Senior/Principal Medical Writing Consultants Pharma IT is hiring experienced Senior/Principal Medical Writer Consultants to join our Regulatory Affairs & Medical Writing Team In this role, you will work as a consultant to support our clients in the Pharma, Biotech and Medical Device industries. In this position, you will work on-site at the client's...

About the RoleGenmab A/S is seeking a highly skilled Senior Disclosure Specialist to join our Clinical Trial Disclosure & Transparency team. As a key member of this team, you will be responsible for executing global and national clinical trial disclosure requirements across Genmab's entire portfolio.Key ResponsibilitiesManage, track, and oversee public...

At Genmab, we're committed to building extraordinary futures together, by developing antibody products and pioneering therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in science, we believe that being...

Sr. Associate/Manager, Clinical Trial Disclosure & Transparency Sr. Associate/Manager, Clinical Trial Disclosure & Transparency Location : This role can be based in Copenhagen, Denmark (DK), or Utrecht, Netherlands (NL), and offers a hybrid work arrangement. Role Overview As a Sr. Associate/Manager in the Clinical Trial Disclosure & Transparency team, you...

About Our TeamOur Clinical Trial Disclosure & Transparency team plays a crucial role in ensuring successful clinical trial conduct and reporting. We recognize the scientific and ethical value of sharing clinical trial information in an unbiased and timely manner, benefiting patients and external stakeholders alike.Job OverviewThis Sr. Associate/Manager...

Company OverviewAbout LEO PharmaWe are an ambitious team driven by a high level of integrity, science, and passion for our work. Our Medical Communication team in Global Clinical Development is responsible for planning, managing, and writing clear, concise, and audience-friendly regulatory, scientific, and medical documents.In this role, you will play a...

Direct message the job poster from ScientaPartnering with Life Science Organizations to Optimize their Hiring Process & Identify the Best TalentPosition Overview: Our client, a commercialized biotech, is looking for an experienced Medical Director specializing in Oncology to lead their global clinical development programs. The successful candidate will...

Direct message the job poster from ScientaPartnering with Life Science Organizations to Optimize their Hiring Process & Identify the Best TalentPosition Overview: Our client, a commercialized biotech, is looking for an experienced Medical Director specializing in Oncology to lead their global clinical development programs. The successful candidate will...

Direct message the job poster from Scienta Partnering with Life Science Organizations to Optimize their Hiring Process & Identify the Best Talent Position Overview: Our client, a commercialized biotech, is looking for an experienced Medical Director specializing in Oncology to lead their global clinical development programs. The successful candidate will...

Disclosure Operations LeadGenmab A/S is an international biotechnology company dedicated to improving the lives of patients through innovative and differentiated antibody therapeutics.Job DescriptionWe are seeking a highly skilled Global Disclosure Operations Lead to join our Clinical Trial Disclosure & Transparency team. As a key member of this team, you...

Responsibilities:Clinical Development Leadership: Manage the direction, planning, execution, and interpretation of clinical trials or research activities across one or more clinical development programs. Ensure that clinical trials are conducted in compliance with applicable regulations, guidelines, and company policies.Clinical Document Development:...

About the RoleAs a Principal Medical Writer Specialist, you will be responsible for leading medical writing projects and collaborating with cross-functional teams to ensure successful outcomes.You will work closely with clients to understand their needs and provide expert-level medical writing services, including clinical document preparation and review.Our...

We are seeking a highly skilled professional to manage our Digital Medical Writing Team as the Digital Medical Writing Team Manager at Lundbeck A/S, H. As a key member of our Global Regulatory Affairs, Medical Documentation, and R&D Quality (GRAMDQ) department, you will play a vital role in shaping our commitment to advancing brain health.This role requires...

Clinical Trial Disclosure & Transparency TeamGenmab A/S is an international biotechnology company with a core purpose guiding its unstoppable team to strive towards improving the lives of patients through innovative and differentiated antibody therapeutics.Job SummaryWe are seeking a motivated and detail-oriented Clinical Trial Transparency Manager to join...

Job OverviewWe are seeking a detail-oriented and organized individual to join our Clinical Trial Disclosure & Transparency team at Genmab A/S. As a Regulatory Affairs Manager Clinical Trials, you will be responsible for ensuring high-quality disclosure of clinical trial information and overseeing the relationship with our disclosure vendor(s) to ensure...