Clinical Research Associate
Há 2 dias
Company Overview
Priovant is a company dedicated to developing therapies for autoimmune diseases. Our goal is to address high unmet needs in this field.
Job Description
We are seeking a Senior Clinical Research Associate to collaborate with investigative study sites and perform site management activities. The ideal candidate will ensure project timelines and deliverables are met, while building strong relationships with site staff and leveraging knowledge of protocol and regulatory guidelines.
The successful candidate will have experience in independent monitoring and be well-organized, with high attention to detail skills and the ability to adapt quickly to changing priorities. They will also be able to propose well-thought-out solutions and interact professionally with Principal Investigators and clinical site staff.
Required Skills and Qualifications
To succeed in this role, you will need:
- A minimum of 4 years of independent monitoring experience, preferably with experience at both CRO and Sponsor
- Deep understanding of ICH, GCP, FDA, and other regulatory guidelines
- Strong knowledge of drug development and clinical research processes
- Familiarity with NDA process and FDA/EMA inspection experience is highly desired
- Experience in Phase II - IV clinical trials preferred
- Risk Based Monitoring, Targeted SDV, and Remote monitoring experience
- Strong technical experience with clinical trial systems (CTMS, EDC, eTMF, ePRO, eREG eSource, EMR, IRT/IXRS, etc.)
- Dependable with a track record of collaborating and making an impact in team settings
- Adaptable with strong prioritization skills across multiple projects
Benefits
This position offers:
- A competitive salary of €60,000 - €80,000 per year, depending on experience
- An opportunity to work with a dynamic company in Porto, Portugal
- A chance to contribute to groundbreaking research and develop your career in clinical research
Salary: €68,000 - €72,000 per year
Eligible to work in Portugal
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