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Job Details

Freelance - Regulatory and Site Services Lead - home or office based - UK/EU

Company: Chiltern
Location: Home or office based - anywhere in the EU/UK
Reference: 899226a
Closing Date: 08 Sep 17
Type: Permanent
Salary (£): On Application
Benefits: Excellent and competitive benefits

Job Summary:

Freelance - RSS Lead - working for Chiltern - home or office based anywhere in the EU/UK

Requirements:

 Job Background

Due to our continuing success and expansion, we are looking to recruit a number of Regulatory and Site Services Leads across Europe.  We can hire staff in the UK/EU.

Chiltern is Europe’s largest privately owned full service (Phase I-IV) Clinical Research Organization, with 4300 employees and offices throughout Europe, both Eastern and Western, North and South America and Asia. We have worked in virtually every therapeutic area for all the major pharmaceutical companies and very many of the smaller ones.

About the department: This department provides an efficient, quality-centric approach to study start-up activities with a growing focus on site relationships. RSS perform regulatory and ethics submissions (initial and amendment), document collection and quality control through all phases of the clinical trial, and execution of site level feasibility in coordination with the Feasibility department.  There are opportunities to develop your career, take on more responsibilities and be involved in cutting edge global studies.

Job Background

Due to our continuing success and expansion, we are looking to recruit a number of Regulatory and Site Services Leads across Europe.  We can hire staff in the UK/EU.

Chiltern is Europe’s largest privately owned full service (Phase I-IV) Clinical Research Organization, with 4300 employees and offices throughout Europe, both Eastern and Western, North and South America and Asia. We have worked in virtually every therapeutic area for all the major pharmaceutical companies and very many of the smaller ones.

Duties:

Expert in, project startup and/or related maintenance activities for a particular study/studies on a regional and/or global level.  Responsible for leading, ensuring and overseeing, startup and/or maintenance activities on projects, on time, within budget, and in compliance with SOPs and/or other quality and regulatory requirements.

Skills:

  • Bachelors degree in biomedical life science, pharmacology or a nursing background is preferred
  • Extensive experience in a clinical research role with a pharmaceutical company and/or CRO, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job
  • Experience in study co-ordination activities across more than one country with start-up co-ordination experience preferred
  • Understanding of the principles of project management, ICH-GCP, and regulatory requirements
  • Leadership and mentoring qualities
  • Understanding of the scope of start-up activities and the challenges faced in start-up
  • Client facing experience is preferred
  • Proficiency with MS Office applications
  • Ability to communicate effectively in English
  • This is a full time permanent role, office or home based

 

Additional information:

To apply for this position please email your CV and covering letter to nicky.cooke@chiltern.com - nicky.cooke@chiltern.com

For more information about Chiltern International, please visit our web site at www.chiltern.com

 Please note that if your experience does not mirror that of our requirements for this role you may not receive a response

 Candidates must be eligible to work in the UK/EU

 

Salary

Negotiable

Position Type

Contract
Full Time or Part Time

Contact

Email Nicky Cooke - Nicky.Cooke@chiltern.com
+44 (0) 1753 216729

 

Apply for this job: Freelance - Regulatory and Site Services Lead - home or office based - UK/EU

Contact Information:

Address:  London, UK
171 Bath Road Slough Berkshire
SL1 4AA, UK
England
Tel:  +44 (0) 1753 512000
Fax:  +44 (0) 1753 511116
Website:  Visit Our Web Site

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