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Job Details

Regulatory Lead CTA

Company: i-Pharm Consulting
Location: Cambridge
Reference: NIBE10018
Closing Date: 09 Dec 16
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

Regulatory Lead CTAMy client, a leading Regulatory Affairs consultancy, is looking for an experienced candidate to join their development team as a CTA lead/Manager. My client works with over 400 global pharmaceutical and biotechnology customers and they need a strong candidate to work co-ordinate and lead a CTA team. Candidates must be eligible to work in the UK. ...

Requirements:

Regulatory Lead CTA

My client, a leading Regulatory Affairs consultancy, is looking for an experienced candidate to join their development team as a CTA lead/Manager. My client works with over 400 global pharmaceutical and biotechnology customers and they need a strong candidate to work co-ordinate and lead a CTA team. Candidates must be eligible to work in the UK.

Job Title: Regulatory Lead/Manager
Location: Cambridge / London / Essex
Benefits: Very good annual salary + benefits

Job Responsibilities
• Manage and co-ordinate CTA
• Responsible for ensuring that submission documentation is maintained in a timely manner
• Leads and co-ordinates a team
• Supports Regulatory management in ensuring compliance for all regulatory and ethic procedures and submissions
• Project Management/lead responsibilities

Ideal Candidate
1. Minimum of a science degree with further education ideal (MSc, PhD)
2. Strong understanding of the regulatory environment including guidelines
3. In depth knowledge of CTA applications
4. Knowledge of ICH/GCP and clinical trial directive
5. Leadership experience would be good
6. Ability to work under pressure and achieve timely submission and regulatory approvals
7. 3+ years’ experience within Regulatory CTA
8. Strong communication style and the ability to liaise directly with clients
9. Ability to project manage

TO APPLY
If you would like to discuss this vacancy further, please call Regulatory Affairs Recruitment Consultant on +44 (0)20 3189 0463, or email nbehan@i-pharmconsulting.com. If this role is not suitable, Niall is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

www.i-pharmconsulting.com

KEY WORDS

Pharmaceutical, Biotech, Biotechnology, Biochemistry, CRO, Pharma, Pharmaceutical, Clinical, Clinical Regulatory Affairs, Regulatory Affairs Manager, Regulatory Affairs Senior Manager, Senior Regulatory Affairs Manager, Regulatory Affairs Management, Reg Affairs, Reg Affairs Manager, Regulatory Affairs Coordinator, Regulatory Affairs Consultant, Principal Consultant, Principal Regulatory Consultant, Regulatory Affairs Associate, Regulatory Affairs Officer, Regulatory Affairs Expert, Regulatory Affairs Specialist, Regulatory Affairs Executive Associate, Submissions, GRA, RA, Regulatory Affairs Submissions Associate, Regulatory Affairs Submissions Coordinator, RA Submissions Coordinator, Senior Regulatory Affairs Associate, Regulatory Submissions, Regulatory, Regulatory Affairs Associate, Regulatory Affairs Associate II, Regulatory Line Management, Oncology, cardiovascular, vaccines, general medicines, CNS, Respiratory, London, England, UK, Greater London, Central London, East London, West London, North London, South London, Cambridge





Apply for this job: Regulatory Lead CTA

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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