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Hans Postlind Location
Basel, BS, CH
Hans Postlind Work
2022 -now Vice President, Clinical Program Planning and Execution, Rdma - Swedish Orphan Biovitrum Ab @
2022 -now Research and Development @
2020 -now Toxicologist @
2017 -2019 Drug Development Consultant @ Hp Life Science Consulting
2015 -2018 Managing Partner @
2015 -2015 Consultant in Drug Development @ Hp Life Science
2013 -2014 Head of Project Leadership, R and D, Bioscience @
2012 -2013 Vice President Non Clinical Development @
2010 -2012 Vice President Portfolio, Project and Alliance Management @
2008 -2010 Head Portfolio Office @
2008 Vice President Preclinical Development @
1998 -2000 Head PPKM @
Hans Postlind Education
Uppsala University 1982-1990
Uppsala University
(Pharmacy)
1982-1986
Hans Postlind Skills
Pharmaceutical Industry
Clinical Development
Pharmacokinetics
Clinical Trials
Drug Discovery
CRO
Drug Development
Pharmacology
Lifesciences
Biotechnology
Medicinal Chemistry
Regulatory Affairs
Pharmacovigilance
GCP
Regulatory Submissions
In Vitro
Pharmaceutics
Chromatography
Biopharmaceuticals
Organic Chemistry
HPLC
Toxicology
Immunology
GLP
Technology Transfer
Pharmaceutical Research
Neuroscience
Drug Delivery
Validation
Clinical Pharmacology
Market Access
Formulation
Oncology
GMP
Regulatory Requirements
Sop
Medical Affairs
IND
Bioanalysis
Drug Design
Biomarkers
Therapeutic Areas
Translational Medicine
R&D
Life Sciences
Hans Postlind Summary
Hans Postlind, based in Basel, BS, CH, is currently a Vice President, Clinical Program Planning and Execution, Rdma - Swedish Orphan Biovitrum Ab at Sobi - Swedish Orphan Biovitrum Ab (Publ). Hans Postlind brings experience from previous roles at Sobi - Swedish Orphan Biovitrum Ab (Publ), Swedish Chemicals Agency, Hp Life Science Consulting and RCP Pharma LLP. Hans Postlind holds a 1982 - 1990 Uppsala University. With a robust skill set that includes Pharmaceutical Industry, Clinical Development, Pharmacokinetics, Clinical Trials, Drug Discovery and more. Hans Postlind has 4 emails on RocketReach.
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