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Study Start-Up Specialist

Czech Republic   •  Negotiable  •  Permanent, Full time


Study Start-Up Specialist

Prague Czech Republic

CRO

Excellent salary and benefits

Are you a recent graduate looking to start your clinical research career?

A global, leading CRO, working within medical devices, pharmaceuticals and biotechnology, have a requirement for a Project Co-ordinator to join their growing team.They work on all major therapeutic areas including cardiology, oncology, central nervous system, endocrinology, metabolic disease, anti-viral and anti-infective whilst following a scientific and disciplined approach.

Key Responsibilities:

Preparation, review, and filing of clinical trial applications

Reporting on regulatory submissions documents and timelines;

Maintaining submission compliance with relevant guidelines and regulations

Keep up to date with changing country regulations and compliance requirements and help implement changes where necesarry

Track submissions and ensure timely filing of documents.

Key Requirements:

Bachelors degree

Strong organisation, communication and attention to detail

Fluency in English and Czech

Proficient in using Microsoft Office

If this role is of interest, please send your CV to Hanna.Poole@cpl.com to apply, or email for further information.

  • Agency: Cpl Life Sciences
  • Contact: Hanna Poole
  • Reference: JO-2201-483547
  • Posted: 14th January 2022
  • Expires: 11th February 2022

Cpl Life Sciences

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