cta

Zealand Pharma A/S is seeking a Regulatory Documentation Specialist to drive the operational delivery of CTA/IND/NDA/MAA/PIP submissions and related documents. You will work closely with RA and cross-functional colleagues, coordinating with CROs and publishers to ensure submission readiness. You will maintain trackers, handle CTIS activities, and act as a...

We are extra[not]ordinary (ex tra not or di nary | ik-ˈstr-not-ȯr-də-ˌner-ē) Adjective: A unique word for Genmab meaning to go way beyond what is usual; to be remarkable; proudly unique and authentic Back to search results Previous job Next job JOB DESCRIPTION At Genmab, we are dedicated to building extra[not]ordinary futures, together, by developing...

Company DescriptionAt Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team,...

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions...

Company DescriptionAt Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.Company DescriptionAt Intuitive, we are united behind our mission: we believe that minimally invasive care is...

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions...

Genmab seeks a Contract Manager to lead end-to-end management of Clinical Trial Agreements (CTAs) and FMV negotiations. You will serve as the primary contract execution contact, ensuring compliance and maintaining inspection-ready records across sites. Strong negotiation and cross-functional collaboration are essential. The role requires experience in...

Zealand Pharma A/S is seeking a Regulatory Documentation Specialist to drive the operational delivery of CTA/IND/NDA/MAA/PIP submissions and related documents. You will work closely with RA and cross-functional colleagues, coordinating with CROs and publishers to ensure submission readiness.You will maintain trackers, handle CTIS activities, and act as a...

Genmab is seeking a Contract Manager to lead end-to-end management of Clinical Trial Agreements (CTAs) and FMV negotiations. You will be the primary contact for trial sites, ensuring contracts meet legal and regulatory requirements and are audit-ready.In this role, you will partner with Legal, Compliance and trial teams to manage budgets, documentation, and...

Company DescriptionAt Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team,...

Company DescriptionAt Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team,...

Job Overview At Genmab, we are dedicated to building extra[not]ordinary® futures together by developing antibody products and groundbreaking KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued...

Zealand Pharma A/S is seeking a Principal Toxicologist to guide safety assessments from discovery through clinical development. You will design nonclinical strategies, oversee studies at CROs, and author regulatory toxicology sections for INDs, CTAs, and NDAs while collaborating with multidisciplinary teams.You will bring a deep toxicology background, drive...

We are extra[not]ordinary(ex tra not or di nary | ik-ˈstr-not-ȯr-də-ˌner-ē)Adjective: A unique word for Genmab meaning to go way beyond what isusual; to be remarkable; proudly unique and authenticBack to search resultsPrevious job Next jobJOB DESCRIPTIONAt Genmab, we are dedicated to building extra[not]ordinary futures, together, by developing antibody...

Does it excite you to keep regulatory submissions on track for one of the industry's most closely watched obesity programs, and do you have a talent for turning cross-functional input into submission-ready documentation? If this sounds like you, and you are ready to take on a broad area of responsibilities across our clinical pipeline, then you could be our...

Does it excite you to keep regulatory submissions on track for one of the industry's most closely watched obesity programs, and do you have a talent for turning cross‑functional input into submission‑ready documentation? If this sounds like you, and you are ready to take on a broad area of responsibilities across our clinical pipeline, then you could be...

Genmab seeks a Contract Manager to lead end-to-end management of Clinical Trial Agreements (CTAs) and FMV negotiations. You will serve as the primary contract execution contact, ensuring compliance and maintaining inspection-ready records across sites.Strong negotiation and cross-functional collaboration are essential. The role requires experience in...

Does it excite you to keep regulatory submissions on track for one of the industry's most closely watched obesity programs, and do you have a talent for turning cross-functional input into submission-ready documentation? If this sounds like you, and you are ready to take on a broad area of responsibilities across our clinical pipeline, then you could be our...

Does it excite you to keep regulatory submissions on track for one of the industry's most closely watched obesity programs, and do you have a talent for turning cross‑functional input into submission‑ready documentation? If this sounds like you, and you are ready to take on a broad area of responsibilities across our clinical pipeline, then you could be...

Does it excite you to work with nonclinical drug development, and do you have experience with preclinical and regulatory toxicology? If this sounds like you, and you are ready to take on a broad area of responsibilities, then you could be our new colleague.Your new positionAs Principal Toxicologist at Zealand Pharma, you will be guiding the safety assessment...