Study Start-up Specialist – Regulatory Submissions,
Global CRO, Permanent
Regulatory Submissions Specialist contractor is required within this global, Top 15 CRO. The position will be home-based in Spain and focused in the ICF review preparation, EC submissions and work with French health authorities to deliver as appropriate.
Requires those confident in start-up activities, happy to work in home-based.
Employing over 5,000 people worldwide as a full service CRO they can boast a client base of the world’s Top 10 Pharmaceutical & Biotech companies. Giving you the chance to span across multiple therapeutic fields (oncology, cardio, respiratory, CNS, neurology etc) and the full clinical development lifecycle work is varied but rewarding. With strong cross-divisions promotion and a friendly, close-knit environment with a strong pipeline and likelihood of extensions on contracts.
Working within this Top 10, leading CRO as a Regulatory Affairs Specialist (Start-up Associate) as an permanent employee.
Submission to MoH
Submission to Ethics Committees
Labeling creation, customization experience
Facilitate the transition of study activities to local CRAs
Fantastic role that offers no travel and financially competitive hourly rate. Apply below immediately to receive full details.
*Proven start up and ICF review experience
*Start-up or CRA employment history
*CRO or Pharma background
*Fluent in English and Spanish
Salary – €negotiable, competitive based on experience, plus benefits
Do not hesitate to apply, varied background will be considered and offer excellent growth within this dynamic, growing CRO.
Find out more about Meet at www.peoplewithchemistry.com
Or contact Keeley Munday on +44(0)2030196022 or email your CV to firstname.lastname@example.org
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