Regulatory Submissions (Study Start-up) Manager

Dauerhaft | Germany, | 9 Monate | Frist: Mittwoch, 24. Januar 2018, 00:00 Uhr
Diese Position ist abgelaufen. Nicht bewerben!

Jobübersicht

Dauerhaft
; Negotiable
Germany
i-Pharm Consulting

Arbeitsbeschreibung


Job Details
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Job 115 of 1000
Regulatory Submissions (Study Start-up) Manager

Company: i-Pharm Consulting
Location: Germany
Reference: GA100118
Closing Date: 24 Jan 18
Type: Permanent
Salary (£): Negotiable
Benefits:


Job Summary:

Regulatory Submissions (Study Start-up) Manager Our client is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. They are active in over 45 countries across the globe. They continue to steadily grow and are looking to add to their team! Their clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. ...


Requirements:

Regulatory Submissions (Study Start-up) Manager
Our client is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. They are active in over 45 countries across the globe. They continue to steadily grow and are looking to add to their team!
Their clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. This position plays a key role in the clinical trial management process at our client. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
- Efficiently manage and successfully execute all aspects of global start-up according to Sponsor specifications;
- Perform quality checks on submission documents and site essential documents;
- Prepare and approve informed consent forms;
- Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and
- Present during bid defenses, general capabilities meetings, and audits.
- More than 5 years of experience in clinical research, preferably with a CRO. Experience may include CRA or project management experience;
- Knowledge and experience with Clinical Trial Applications within Europe; and
- Strong oral and written communication skills.
- Fluency in English and local language.
Travel: Minimal


Contact Information:
Address:  Head Office
212 New King’s Road London
SW6 4NZ
England
Reasons to work for i-Pharm Consulting
Tel:  +44 (0) 20 3189 2299
Website:  Visit Our Web Site

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