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. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a
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Location - Copenhagen The Medical Lead is responsible for the Medical Affairs Tactics in line with the overall strategy for the Therapeutic Area as well as the Medical Engagement plans. Further
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-clinical, clinical trial data post-marketing, literature) throughout the development and post-approval process in an appropriate and timely manner • Initial development and ongoing maintenance of safety
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Primary Location: Barcelona, Spain (hybrid) Alternate Location: United Kingdom (remote) About this role: As our Global Program Safety Lead within the CRM therapeutic area you will provide scientific
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the development and post-approval process. • Responsible for documentation/tracking/record keeping of the assigned compounds medical safety activities. • Is responsible for initial development and ongoing
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); ensuring that this team reviews all medical safety data from various sources (e.g. pre-clinical, clinical trial data post-marketing, literature) throughout the development and post-approval process in