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Job Details

Senrior Regulatory Affairs Consultant (m/w) Preclinical

Company: i-Pharm Consulting
Location: München
Reference: CRN9997
Closing Date: 22 Nov 17
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

Senior Regulatory Affairs Consultant (m/w) PreclinicalOffice-based in Munich / Full-time, permanentJob Description:- Consulting clients on a wide range of regulatory and technical problems through all stages of product development;- Train, mentor and lead project teams specifically in the product development stages building up to market authorization;- Positioning, regulatory problem solving and regulatory strategy development;- Gap analyses of dossiers at all stages of development;- Writi ...

Requirements:


Senior Regulatory Affairs Consultant (m/w) Preclinical
Office-based in Munich / Full-time, permanent


Job Description:


- Consulting clients on a wide range of regulatory and technical problems through all stages of product development;

- Train, mentor and lead project teams specifically in the product development stages building up to market authorization;

- Positioning, regulatory problem solving and regulatory strategy development;

- Gap analyses of dossiers at all stages of development;

- Writing documents for submission and generating of dossiers for a wide range of product types;

- Representation of clients at regulatory agency meetings, participation and contribution to presubmission meetings, scientific advice meetings

- You will focus on Early Phase Development, including preclinical documents, toxicology reports and the transition into clinical trials from a regulatory perspective.



Requirements:


- Degree in life sciences, ideally medicine, pharmacy, biology or chemistry

- 5 or more years of experience in the field of Regulatory Affairs in the pharmaceutical industry

- Master of Regulatory Affairs (DGRA/EUCRAF) preferred, but not a must

- Experience with Early Development, Preclinical Development and Toxicology

- Good communication, interpersonal interaction, project management and organizational skill essential

- Fluent in English and German, with strong negotiation skills in both languages

- Ability to multitask with exceptional time management skills

- Customer-oriented approach



To Apply:


i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in Europe and Germany. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device,
Biotechnology Contract Research Organizations (CROs) and Contract Manufacturing Organizations (CMO’s). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance, drug safety and Bioinformatics.

www.i-pharmconsulting.com


If you would like to discuss this vacancy further, please call Recruitment Consultant Christian Rommerskirchen on +49 89 71 677 25 41 or email: crommerskirchen@i-pharmconsulting.com.
If this role is not suitable, Christian is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

Apply for this job: Senrior Regulatory Affairs Consultant (m/w) Preclinical

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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