ServiceUpdated on 22 May 2026
Medical and Scientific Writing
Business Development Lead – EMEA & APAC at DLRC Regulatory Consultancy
London, United Kingdom
About
DLRC consultants, and a team of dedicated medical writers, have considerable experience of medical and scientific writing across a wide range of therapeutic areas and classes of molecules, including non-clinical, clinical and quality aspects. DLRC has a flexible approach, therefore, consultants can write regulatory submissions in their entirety, write documents in collaboration with clients, or provide strategic support and review to clients authoring their own medical and scientific documents.
How can we help?
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Clinical Trial Documents
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Clinical Study Reports (CSRs)
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Global Submission Documents
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Annual and Safety Reports
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SOPs and Controlled Documents
Type
- Consulting
Applies to
- Biology/Biotechnology
- Life Science
- Medicine
- Therapeutic Area
Organisation
Similar opportunities
Service
- Medicine
- Consulting
- Life Science
- Therapeutic Area
- Biology/Biotechnology
Ankita Jain
Business Development Lead – EMEA & APAC at DLRC Regulatory Consultancy
London, United Kingdom
Service
- Medicine
- Consulting
- Life Science
- Therapeutic Area
- Biology/Biotechnology
Ankita Jain
Business Development Lead – EMEA & APAC at DLRC Regulatory Consultancy
London, United Kingdom
Service
Expert CDMO for Complex Biologics from Development through Manufacturing
- Development
- Life Science
- Manufacturing
- Biology/Biotechnology
Sabrina Schubert
Associate Director Business Development at KBI Biopharma
Plan-Les-Ouates, Switzerland