JOB DESCRIPTION
Contract Type
Candidate (Freelancer)
Company Type
Pharma
Company Size
Small 100 – 1000
Requested Expertise
Pharmaceutical Product Development / Quality /
Profile Required
pharmaco-toxicological expert
Project Description
You will be in charge of building & drafting pharmaco-toxicological dossier as part of the regulatory dossier (CTD, DT): – assessment report of biological risk, toxicological risk & environmental risk – literature review using pharmaco-toxicological databases – read-across or predictive studies using QSAR in line with international regulatories requirements – manager vendors (brief, quote, review, follow-up, deliverables…) – be the interface for pharmaceutical development, analytical & regulatory affairs – participate actively to Quality Assurance within R&D
Therapeutic Area
All
Language
English,German (only Standard German)
Seniority Level
Experience 5 – 10 years
Starting Date
2022-09-18
Project Duration
12 months
FTE / nb of days per week
5
Project Location
Frankfurt, Germany
Remote Flexibility
Yes
Travel Expected
No
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