Tatiana Asie
Tell me more about Tatiana Asie?
Tatiana Asie is a highly experienced Regulatory Affairs specialist with 14.6 years of work experience in the pharmaceutical industry. Based in Ukraine, she has expertise in regulatory affairs, submissions, clinical trials, and pharmacovigilance. Tatiana has worked at MSD Sharp & Dohme GmbH, a leading pharmaceutical manufacturing company, in the United States, where she held the position of Ra Specialist In Cis in the Other department. With a strong background in GMP and pharmaceutics, Tatiana is skilled in market access and market access.
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About
Regulatory Affairs specialist at MSD Sharp & Dohme GmbH
Work Experience
RA Specialist In CIS
Pharmaceutical Manufacturing
Tatiana Asie's Professional Milestones
- RA Specialist In CIS (2009-02-01~): Optimized CA system performance by implementing advanced CRM technology.
Skill
Pharmaceutical Industry
Regulatory Affairs
Regulatory Submissions
Clinical Trials
Pharmacovigilance
Gmp
Pharmaceutics
Pharmaceutical Sales
Market Access
Sop
Gcp
Certification
Colleagues
Amie Qin
Data Product Owner
Hendyono Lim
application management services lead | aws practitioner | finops certified practitioner | devsecops | itil 4 | agile product owner | certified agile service manager
Henry QIN
pharma b2b technical product owner
July Verhoosel
Planner | Owner
Barbara Brezni
owner @wooden house brezni
Other Named Tatiana Asie
Frequently asked questions
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Tatiana Asie's social media include: Linkedin,
Tatiana Asie works for MSD
Tatiana Asie's role in MSD is RA Specialist In CIS
Tatiana Asie works in the industry of Pharmaceutical Manufacturing
Tatiana Asie's colleagues are Amie Qin,Hendyono Lim,Henry QIN
Tatiana Asie's latest job experience is RA Specialist In CIS at MSD