Study Start-Up Specialist

Role – Study Start-Up Specialist                                

Location – Prague, Czech Republic  

Rate – Competitive in line with skills and experience

Type – Permanent

For one of Planet Pharma global clients we urgently seek a talented Submissions Specialist to join on a permanent basis. In this role you will within a team to accomplish tasks and projects that are instrumental to the company’s success.

Responsibilities

• Prepare, review, and file clinical trial applications to domestic and international regulatory agencies;
• Ensure submissions comply with applicable regulations and guidance documents;
• Advise sponsors on changing regulations and compliance requirements; and
• Track submissions and ensure timely filing of documents.

Requirements

• Bachelor's degree in life sciences;
• At least one year of work experience as a Regulatory Submissions Coordinator
• Excellent organization and communication skills;
• Hands-on experience preparing, reviewing, and submitting regulatory documentation;

To Apply

If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone on +44 (0)20 3928 6631 or email on mowusu-ansah@planet-pharma.co.uk 

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. Planet Pharma is an Employment Agency providing Global Staffing services