Medical Writing and Clinical Disclosure Professional

Your Role: As a Medical Writing and Clinical Disclosure Professional, you will play a crucial part in planning, managing, and writing clear, concise, and audience-friendly regulatory, scientific, and medical documents. Your main tasks will include:Writing and editing original regulatory, scientific, and medical documents at a professional level.Leading and...

About UsGenmab is an international biotechnology company driven by its core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. Our team strives towards transforming cancer treatment and serious diseases, fostering a collaborative environment where employees can thrive.As a Sr. Associate/Manager in our...

Job DescriptionWe are seeking a Senior/Principal Medical Writing Consultant to join our team. As a key member of our Regulatory Affairs & Medical Writing Team, you will work as a consultant to support our clients in the Pharma, Biotech, and Medical Device industries.In this role, you will be responsible for writing and reviewing clinical (and nonclinical)...

Clinical Documentation SpecialistWe are looking for a skilled Clinical Documentation Specialist to join our Regulatory Affairs & Medical Writing Team at Pharma IT.In this role, you will be responsible for writing and reviewing clinical and nonclinical documents for regulatory submissions in the EU and US, including Module 2.5, 2.7, 2.4, 2.6, integrated...

At Genmab A/S, we are committed to transforming the lives of patients through innovative cancer treatment. We are seeking a highly skilled Sr. Associate/Manager, Clinical Trial Disclosure & Transparency, to join our team.Key Responsibilities:Manage and oversee public disclosure of clinical trial protocols, results, and document redaction.Develop and maintain...

We are seeking a highly motivated and organized Sr. Associate/Manager, Clinical Trial Disclosure & Transparency, to join our team at Genmab A/S. In this role, you will be responsible for managing and overseeing public disclosure of clinical trial protocols, results, and document redaction.Key Skills and Qualifications:Strong understanding of clinical...

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...

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...

Company Overview: We are an ambitious team driven by a high level of integrity, science, and passion for our work. Our goal is to create a collaborative atmosphere where you can reach out to a colleague or manager for support and sparring.Job Description: In this role, you will be responsible for planning, handling, managing, structuring, and writing clear,...

About the RoleThe ideal candidate for this position holds at least 10 years of experience within drug development in the pharma/biotech industry, with at least 5 years of experience in medical writing. Understanding of international regulations, ICH guidelines, and document preparation and production (CTDs) is required.A strong understanding of clinical...

Our PurposeWe are committed to promoting transparency in clinical trial research at Genmab. We recognize the scientific and ethical value of sharing clinical trial information in an unbiased and timely manner, benefiting patients and external stakeholders alike. Our Clinical Trial Disclosure & Transparency team plays a crucial role in ensuring successful...

Clinical Documents SpecialistWe are looking for a skilled Clinical Documents Specialist to join our Regulatory Affairs & Medical Writing Team at Pharma IT.In this role, you will be responsible for writing and reviewing clinical and nonclinical documents for regulatory submissions in the EU and US, including Module 2.5, 2.7, 2.4, 2.6, integrated summaries of...

In our line of work, life isn't a given - it's the ultimate goal. When life takes an unexpected turn, our technology and solutions enable caregivers to make informed diagnostic decisions to improve patient care. This is our shared purpose at Radiometer and what unites all +4000 of us - no matter our roles or where in the world we're located. Creating...

Medical Writing Expert ConsultantWe are seeking an experienced Medical Writing Expert Consultant to join our Regulatory Affairs & Medical Writing Team at Pharma IT.In this role, you will work as a consultant to support our clients in the pharmaceutical, biotechnology, and medical device industries. You will be responsible for writing and reviewing clinical...

Absorb knowledge and apply advanced medical skills as a Medical Advisor within AbbVie's Neuroscience team. Develop your career with us and represent the affiliate's medical/scientific voice of expertise for assigned products in the field of neuroscience.Responsibilities:Maintain professional relationships with experts and academic centersDeliver scientific...

The RoleIQVIA Argentina is seeking a Medical Monitor Professional to join our team. The ideal candidate will have experience in clinical research and be able to monitor clinical studies effectively.Key ResponsibilitiesMonitor clinical sites to ensure compliance with Good Clinical Practice (GCP).Collaborate with sites to develop and track subject recruitment...

Clinical Operations Manager - Rare Diseases is a vital role within Lundbeck A/S, H's Global Clinical Trial team. As a seasoned professional in the field, you will leverage your expertise to manage clinical trials in rare diseases, working collaboratively with internal stakeholders and external partners.Job DescriptionYour primary responsibility will be to...

Why Join UsWe are a unique organization that offers a chance to influence the future of dental imaging. As a member of our team, you will have the opportunity to work on innovative projects, collaborate with skilled colleagues, and contribute to the development of cutting-edge solutions.Our team is dedicated to bringing CBCT scanning to the next level by...

Radiometer Danmark / Danaher is a leading innovator in medical diagnostics, committed to empowering healthcare professionals with cutting-edge tools and technologies. We are seeking a talented Clinical Expert Partner to drive key internal and external medical and scientific activities to support our current portfolio and shape future development in acute...