cro oversight

Job ID: 7226We are looking for credit risk experts to contribute to the good credit quality of Nordea. Job ID: 7226We are looking for credit risk experts to contribute to the good credit quality of Nordea. About Our Teams Meet the Credit Risk Control and CRO Delegates teams within Group Credit Risk. Our role is to add value by controlling and monitoring...

Zealand Pharma A/S seeks a Head of Clinical Trial Documentation to lead a seven‑strong team and own TMF, trial administration, and related processes. You will oversee eTMF in Veeva Vault, ensure quality oversight of CROs and internal stakeholders, and drive readiness for inspections across global trials. The role combines leadership with hands‑on...

Zealand Pharma A/S seeks a Head of Clinical Trial Documentation to lead a seven‑strong team and own TMF, trial administration, and related processes. You will oversee eTMF in Veeva Vault, ensure quality oversight of CROs and internal stakeholders, and drive readiness for inspections across global trials.The role combines leadership with hands‑on...

Does it excite you to lead a team and own the processes and systems behind our clinical trial documentation, and do you have experience with ICH-GCP and Trial Master File (TMF)? 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 position As Head of Clinical Trial...

Does it excite you to lead a team and own the processes and systems behind our clinical trial documentation, and do you have experience with ICH-GCP and Trial Master File (TMF)? 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 position As Head of Clinical Trial...

Does it excite you to lead a team and own the processes and systems behind our clinical trial documentation, and do you have experience with ICH-GCP and Trial Master File (TMF)? 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 position** As Head of Clinical Trial...

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...

Key Responsibilities Support the planning, setup, and execution of global clinical trials, ensuring activities are delivered in accordance with timelines, quality standards, and regulatory requirements. Ensure trial oversight by maintaining accurate documentation and participating in inspection readiness activities. Collaborate with CROs and internal...

Summary This position reports to the Head of Clinical Operations,This role is responsible for leading the development, planning, launch, conduct, closure, and submission of Gan & Lee sponsored clinical trials in accordance with all applicable federal, state, and local laws/regulations and Company’s policies, procedures, and guidelines. The Senior Clinical...

Join a leading international life science company in an exciting role and assume end-to-end responsibility for a high-impact role at the intersection of operational strategy and execution. Lead a Complex Global Clinical Study with strategic impact As Clinical Trial Program Lead, you will play a key role in shaping and executing the company’ clinical...

Your impact begins here. As GLP QA Professional, you will help ensure non-clinical research at Novo is carried out to Good Laboratory Practice (GLP) standards. You will oversee studies, inspect internal and external work, and turn what you see into clear, practical recommendations that keep research reliable and moving. You will shape how quality is built...

Your impact begins here As GLP QA Professional, you will help make sure non-clinical research at Novo is carried out to Good Laboratory Practice (GLP) standards. You will oversee studies, inspect internal and external work, and turn what you see into clear, practical recommendations that keep research reliable and moving. You will shape how quality is built...

As GLP QA Professional, you will help make sure non-clinical research at Novo is carried out to Good Laboratory Practice (GLP) standards. You will oversee studies, inspect internal and external work, and turn what you see into clear, practical recommendations that keep research reliable and moving. You will shape how quality is built into non-clinical...

Director, Clinical Administration & Compliance About the job Director, Clinical Administration & Compliance Join Pharmacosmos in a newly established function, in a role combining people leadership with direct involvement in clinical processes, compliance and continuous improvement. Build and lead a new Clinical Administration & Compliance functionAs...

Reporting to: Director, Bioanalytics About Hemab Hemab is building preventative treatments for serious, underserved bleeding disorders. These are therapies designed to work with the body's own biology and stop bleeds before they start, instead of treating them after they happen. We're patient-first, science-led and clinical-stage - with a pipeline that...

Does it excite you to work with drug metabolism and pharmacokinetics across peptides, proteins and small molecules, and do you have experience with in vitro ADME assays and liquid chromatography-mass spectrometry (LC-MS) bioanalysis? If this sounds like you, and you are ready to take on a broad area of responsibilities, then you could be our new colleague....

Does it excite you to work with drug metabolism and pharmacokinetics across peptides, proteins and small molecules, and do you have experience with in vitro ADME assays and liquid chromatography-mass spectrometry (LC-MS) bioanalysis? If this sounds like you, and you are ready to take on a broad area of responsibilities, then you could be our new...

Does it excite you to work with drug metabolism and pharmacokinetics across peptides, proteins and small molecules, and do you have experience with in vitro ADME assays and liquid chromatography-mass spectrometry (LC-MS) bioanalysis? If this sounds like you, and you are ready to take on a broad area of responsibilities, then you could be our new...

Does it excite you to work with drug metabolism and pharmacokinetics across peptides, proteins and small molecules, and do you have experience with in vitro ADME assays and liquid chromatography-mass spectrometry (LC-MS) bioanalysis? If this sounds like you, and you are ready to take on a broad area of responsibilities, then you could be our new...

Are you ready to ensure that patients worldwide receive uninterrupted access to innovative clinical trial treatments? Join Novo Nordisk and play a central role in driving clinical supply strategies across global trials. This is your opportunity to combine operational excellence, stakeholder collaboration, and supply expertise to support life-changing...