ELC GROUP is one of the most reputable regulatory affairs organizations in Europe and a leading provider of Regulatory services to Pharmaceutical, Biotech, Generic, and Medical Device companies supporting their clinical development, pre & post marketing obligations.
We provide customised solutions which ensure fast and successful development, authorisation or maintenance of our client's products.
ELC GROUP Regulatory team provides a global service offering with offices located in Prague (Czech Republic), Ahmedabad (India) and Cambridge (UK). Our Regulatory Affairs team is a highly experienced group of professionals who have the expertise to help develop your research into revenue.
Post: Preclinical/Clinical Project Manager
Job Description:
- Vendor Coordination for preclinical and clinical studies
- Review of preclinical and clinical study documentation
- Monitoring and audit of preclinical and clinical study activities
- Organization of preclinical and clinical study activities
- Ensure compliance with company SOPs, ICH GCP, GLP and regulatory requirements
Requirements:
- Qualification: Pharmacy Degree
- The successful candidate will have 3-4 years working as a CRA at pharma company / CRO
- Preclinical research experience will be preferred
- Languages: Must have excellent written and oral communication skills in English and Russian
- Willingness to travel
- Ability to manage multiple projects
Additional Information:
Experience: 3-4 years
Location: Prague
Education: Pharmacy Degree
Industry Type: Pharma/ Healthcare/ Clinical research
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