Clinical Documentation Specialist
3 days ago
Lundbeck is seeking a highly skilled Clinical Submission Coordinator to join our Medical Documentation team. As a key member of our team, you will be responsible for managing clinical documentation and ensuring the submission readiness of clinical trial reports and clinical submission documents across our clinical development programmes.
Your Key Responsibilities- Manage clinical documentation and ensure the electronic integrity of the documentation
- Ensure compliance with internal and external standards and requirements
- Assist in the production of documents and perform quality control
- Be involved in activities to ensure public transparency of Lundbeck's clinical research
You will be part of a dynamic team that drives the development of clinical and regulatory documents. We are a collaborative and imaginative team that uses our writing, story-lining, and collaboration skills to ensure that scientific information and clinical data are presented clearly and concisely.
What We Offer- A rewarding career with a mix of exciting tasks and development opportunities
- A positive and engaged working climate
- Flexible working conditions
- Opportunities for growth and professional development
- Degree in life science and knowledge of the pharmaceutical industry
- Strong organizational skills and a methodological approach to work
- Drive for and experience with how IT and systems can facilitate processes and procedures
- Experience with clinical documentation, ideally related to clinical trials
- Familiarity with Documentum-based systems and advanced knowledge in word-processing programs and how they can be applied to clinical documentation
- Strong interpersonal and communication skills in a global environment
- Fluency in spoken and written English
If you are a motivated and detail-oriented individual with a passion for clinical documentation, we encourage you to apply for this exciting opportunity. Please upload your CV and include a few lines about your motivation for applying. We look forward to hearing from you
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Clinical Documentation Specialist
3 weeks ago
Copenhagen, Copenhagen, Denmark Lundbeck Full timeJob SummaryLundbeck is seeking a highly skilled Clinical Documentation Specialist to join our team. As a Clinical Documentation Specialist, you will be responsible for managing clinical documentation and ensuring the submission readiness of clinical trial reports and clinical submission documents across Lundbeck's clinical development programmes.Key...
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Clinical Documentation Specialist
3 weeks ago
Copenhagen, Copenhagen, Denmark Lundbeck Full timeJob SummaryLundbeck is seeking a highly skilled Clinical Documentation Specialist to join our team. As a key member of our Medical Documentation department, you will be responsible for managing clinical documentation and ensuring the submission readiness of clinical trial reports and clinical submission documents across Lundbeck's clinical development...
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Clinical Documentation Specialist
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Copenhagen, Copenhagen, Denmark Lundbeck Full timeAbout the RoleLundbeck is seeking a highly skilled Clinical Submission Coordinator to join our Medical Documentation team. As a key member of our team, you will be responsible for managing clinical documentation and ensuring the submission readiness of clinical trial reports and clinical submission documents across our clinical development programmes.You...
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Clinical Documentation Specialist
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Copenhagen, Copenhagen, Denmark Lundbeck Full timeJob Title: Clinical Submission CoordinatorLundbeck is seeking a highly organized and detail-oriented Clinical Submission Coordinator to join our Medical Documentation team. As a key member of our team, you will be responsible for managing clinical documentation and ensuring the submission readiness of clinical trial reports and clinical submission documents...
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Clinical Documentation Specialist
2 weeks ago
Copenhagen, Copenhagen, Denmark Lundbeck Full timeJob Title: Clinical Submission CoordinatorLundbeck is seeking a highly organized and detail-oriented Clinical Submission Coordinator to join our Medical Documentation team. As a key member of our team, you will be responsible for managing clinical documentation and ensuring the submission readiness of clinical trial reports and clinical submission documents...
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Clinical Documentation Specialist
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Copenhagen, Copenhagen, Denmark Lundbeck Full timeAbout the RoleLundbeck is seeking a highly skilled Clinical Submission Coordinator to join our Medical Documentation team. As a key member of our team, you will be responsible for managing clinical documentation and ensuring the submission readiness of clinical trial reports and clinical submission documents across Lundbeck's clinical development...
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Clinical Documentation Specialist
2 weeks ago
Copenhagen, Copenhagen, Denmark Lundbeck Full timeAbout the RoleLundbeck is seeking a highly skilled Clinical Submission Coordinator to join our Medical Documentation team. As a key member of our team, you will be responsible for managing clinical documentation and ensuring the submission readiness of clinical trial reports and clinical submission documents across our clinical development programmes.Your...
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Copenhagen, Copenhagen, Denmark Lundbeck Full timeAbout the RoleLundbeck is seeking a highly skilled Clinical Submission Coordinator to join our Medical Documentation team. As a key member of our team, you will be responsible for managing clinical documentation and ensuring the submission readiness of clinical trial reports and clinical submission documents across our clinical development programmes.Key...
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Copenhagen, Copenhagen, Denmark Lundbeck Full timeAbout the RoleLundbeck is seeking a highly skilled Clinical Submission Coordinator to join our Medical Documentation team. As a key member of our team, you will be responsible for managing clinical documentation and ensuring the submission readiness of clinical trial reports and clinical submission documents across our clinical development programmes.Key...
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