Budhesh Dhamija Email & Phone Number
Director, Clinical Regulatory Affairs @ ITM Isotope Technologies Munich SE
Budhesh Dhamija's Location
Frankfurt Am Main, Hesse, Germany
Budhesh Dhamija's Work
- Director, Clinical Regulatory Affairs @ ITM Isotope Technologies Munich SE
- Team Leader Clinical Regulatory Affairs @ ITM Isotope Technologies Munich SE
- Senior Strategist Clinical Regulatory Affairs @ ITM Isotope Technologies Munich SE
- Senior Manager, Regulatory Intelligence and Policy @ CSL Behring
- Regulatory Regional Manager EU @ CSL Behring
- Senior Regulatory Affairs Professional- Victoza team @ Novo Nordisk
- Senior Safety Surveillance Medical Writer @ Novo Nordisk
- Safety Medical Writer and Advisor @ Novo Nordisk
- Medical writing-Consultant for Novo Nordisk @ S-cubed
- Team Lead - Medical Writing @ APCER PHARMA
Budhesh Dhamija's Education
- Manipal Academy of Higher Education
Masters in Pharmacy (Pharmacy (Pharmaceutical Marketing))
2004 - 2006 - Institute of Clinical Research (India)
Post Graduate Degree in Advanced Clinical Research (Clinical Research and Medical Writing)
2007 - 2008 - Delhi University
Bachelors in Pharmacy (Pharmacy)
2000 - 2004
Budhesh Dhamija's Skills
- Clinical Trials
- Medical Writing
- Ich Gcp
- Selling Skills
- Clinical Research
- Good Clinical Practice Gcp
- Regulatory Affairs
- Medical Devices
- Sop
- Pharmacovigilance
Budhesh Dhamija's Summary
Budhesh Dhamija, based in Frankfurt Am Main, Hesse, Germany, is currently a Director, Clinical Regulatory Affairs at ITM Isotope Technologies Munich SE, bringing experience from previous roles at ITM Isotope Technologies Munich SE and CSL Behring. Budhesh Dhamija holds a 2004 - 2006 Masters in Pharmacy in Pharmacy (Pharmaceutical Marketing) @ Manipal Academy of Higher Education. With a robust skill set that includes Clinical Trials, Medical Writing, Ich Gcp, Selling Skills, Clinical Research and more, Budhesh Dhamija contributes valuable insights to the industry. Budhesh Dhamija has 4 emails and 2 mobile phone numbers on RocketReach.
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