I will conduct clinical research, manage clinical trial and data
PhD Pharmacist, Clinical Research Scientist and Medical Writer
About this Gig
Do you need expert clinical data analysis, pharmacovigilance reporting, or regulatory documentation for your pharmaceutical or biotech company?
I am Dr. Arfat Yameen, a PhD pharmacist and active clinical research scientist at Continuum Research Center (CRO) with 15+ years of industry experience.
What I offer:
- Clinical trial data analysis and statistical reporting
- Pharmacovigilance and drug safety reporting for industry clients
- Regulatory document preparation for pharmaceutical submissions
- SOP writing and clinical trial protocol development for CROs
- Drug efficacy and safety data interpretation
- GCP-compliant clinical research documentation
WHY CHOOSE ME:
- PhD in Microbiology from Quaid-i-Azam University
- Active scientist at Continuum Research Center (CRO)
- Experience with GCP, ICH, FDA, and EMA regulatory standards
- Trusted by international pharma and biotech companies
Order now for expert, GCP-compliant clinical research services!
Service type:
Research
Language:
English
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