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Level: Guru
Member Since: 14/07/2017

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First name Diana
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I am the Head of Scientific and Medical Affairs and Senior Scientific Lead at IAG. http://imageanalysisgroup.com. Sn. Scientific Lead to advise and direct the development and execution of imaging as a measure of efficacy, eligibility and safety in drug development. With 10+ years in medical imaging, strategic drug development expertise, PhD in computational neuroimaging and hands-on work with world-leading clinical institutions. I work with biotech and pharma to bring imaging expertise into clinical trial design, advise bio-pharma clients on regulatory pathways and trial management. With extensive experience of planning and directing all functions of clinical trial designs in line with stringent ICH/GCP guidelines and FDA regulations, compliance and quality assurance standards, Diana is responsible for all aspects of clinical trial management, including monitoring clinical investigations, imaging endpoint study design, and clinical trial analysis. Specialities: Solid Tumours, Immuno-Oncology, Inflammation Rare Diseases & Orphan Drugs. My background is in medical computer science, medical devices, CAD software, advanced therapies and digital health and healthcare start ups.

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Name

Diana

I have professional experience in:

Biotechnology, Business strategy, Clinical strategy, Diagnostics, Digital health, Market access, Medical devices, Regulatory affairs, Pharmaceuticals, Startups

Help us confirm that you're an expert

I am the Head of Scientific and Medical Affairs and Senior Scientific Lead at IAG. http://imageanalysisgroup.com. Sn. Scientific Lead to advise and direct the development and execution of imaging as a measure of efficacy, eligibility and safety in drug development. With 10+ years in medical imaging, strategic drug development expertise, PhD in computational neuroimaging and hands-on work with world-leading clinical institutions. I work with biotech and pharma to bring imaging expertise into clinical trial design, advise bio-pharma clients on regulatory pathways and trial management. With extensive experience of planning and directing all functions of clinical trial designs in line with stringent ICH/GCP guidelines and FDA regulations, compliance and quality assurance standards, Diana is responsible for all aspects of clinical trial management, including monitoring clinical investigations, imaging endpoint study design, and clinical trial analysis. Specialities: Solid Tumours, Immuno-Oncology, Inflammation Rare Diseases & Orphan Drugs. My background is in medical computer science, medical devices, CAD software, advanced therapies and digital health and healthcare start ups.

LinkedIn

http://www.linkedin.com/in/dianaroettger

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Last Name

Roettger