Trial Disclosure Specialist

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

Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our Clinical Trials team at Genmab A/S. As a key member of the team, you will be responsible for executing global and national clinical trial disclosure requirements across our entire portfolio.You will work closely with trial teams to ensure high-quality disclosure of clinical...

Job DescriptionWe are seeking a highly skilled Clinical Trials Disclosure Manager to join our team in Copenhagen or Utrecht.Your primary responsibility will be to ensure the disclosure of clinical trial protocols, results, and document redaction across our entire portfolio. You will work closely with trial teams to develop and maintain timelines for protocol...

Job DescriptionAs a Regulatory Affairs Specialist in our Clinical Trials team, you will be responsible for executing global and national clinical trial disclosure requirements across our entire portfolio.Key responsibilities include managing the public disclosure of clinical trial protocols, results, and document redaction, developing and maintaining...

About UsGenmab is a pioneering biotechnology company dedicated to developing innovative antibody products that transform the lives of patients suffering from cancer and serious diseases. Our mission is to build extraordinary futures together by leveraging cutting-edge science and technology to create therapies that make a meaningful difference in people's...

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

Job OverviewAs a Regulatory Affairs Specialist in our Clinical Trials team, you will play a crucial role in ensuring the successful execution of global and national clinical trial disclosure requirements across our portfolio.Your key responsibilities will include managing the public disclosure of clinical trial protocols, results, and document redaction,...

As a Global Disclosure Manager at Genmab A/S, you will play a crucial role in ensuring high-quality disclosure of clinical trial information and implementing new transparency requirements. You will be responsible for supporting trial teams, developing and maintaining timelines for protocol registration and results disclosure, and overseeing the relationship...

Job SummaryGenmab is seeking a highly skilled Sr. Associate/Manager to join our Clinical Trial Disclosure & Transparency team. In this role, you will be responsible for ensuring the successful execution of global and national clinical trial disclosure requirements, supporting trial teams, and overseeing the relationship with our disclosure vendor(s). Your...

About the OpportunityWe're expanding our Clinical Trial Disclosure & Transparency team with a Sr. Associate/Manager position. This role offers a unique chance to work collaboratively with a talented team of professionals who share your passion for making a difference in patients' lives. As a key member of our team, you'll be instrumental in executing global...

Key ResponsibilitiesThe ideal candidate will have previous experience with clinical trial disclosure and a strong understanding of the pharmaceutical industry.They will be responsible for managing the public disclosure of clinical trial protocols, results, and document redaction, developing and maintaining timelines for protocol registration and results...

Company OverviewAt Genmab, we're committed to pushing the boundaries of what's possible in biotechnology. Our unwavering dedication to improving patient outcomes drives us to develop innovative treatments that change lives. We're passionate about fostering a culture of collaboration, creativity, and excellence, where our employees can thrive and grow...

About the RoleThe Global Trial Transparency Lead will play a critical role in ensuring Genmab's adherence to relevant industry guidelines. You will be responsible for monitoring the external landscape, assessing technology needs, and implementing required software solutions.As a key member of our team, you will oversee the relationship with our disclosure...

About GenmabGenmab 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.We are committed to fostering workplace diversity at all levels of the company and believe it is essential for our continued success. We...

At Novo Nordisk A/S, we develop, manufacture, and distribute drug candidates for clinical trials. We are committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve, and the communities we operate in.We are seeking a highly skilled Protein Purification Specialist to join our R&D team. As a Protein...

At MSD Danmark ApS, we are seeking a highly skilled Clinical Research Associate Specialist to join our team. This role is an excellent opportunity for individuals who are passionate about conducting clinical trials and ensuring high site performance.The successful candidate will be responsible for managing assigned trials and sites, working closely with the...

About Novo Nordisk A/SWe are a global biopharmaceutical company dedicated to improving human health through innovative treatments and therapies. Our research and development activities focus on creating novel approaches for treating chronic diseases.Our Product & Process Development team is responsible for developing, manufacturing, and distributing drug...

In this exciting role, you will join our growing department with an anticipated future expansion of new drug candidates. As a CMC Development Quality Assurance Specialist, you will support the progression of our pipeline of promising drug candidates by ensuring patient safety and GMP compliance of the IMP for clinical trials.Your responsibilities will...

Job DescriptionThe Senior Clinical Research Scientist will contribute to the implementation of the global development strategy, leading or co-leading one or more clinical trials in a therapeutic area for one or more compounds in early clinical development.This position involves:Leading or co-leading clinical trials in a therapeutic area for one or more...

About Novo Nordisk A/SWe are a proud life-science company, inspired by life in all its forms and shapes. Our research and development activities focus on creating innovative treatments for patients with chronic diseases across the world.Our team within Product & Process Development makes a real difference for patients by developing, manufacturing, and...