Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Job Details

Country Approval Specialist, SIA - Israel-147256

Company: PPD
Location: Europe, Middle East & Africa-Israel-Tel Aviv Metro
Reference: 147256
Closing Date: 25 Oct 18
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. ...

Requirements:

PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations.
With offices in 47 countries and approximately 20,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help clients and partners bend the cost and time curve of drug development to deliver life-changing therapies that improve health.


PPD is recruiting a Country Approval Specialist (CAS) for our Site and Patient Access department in our Tel Aviv office. The Country Approval Specialist will manage the preparation, review and coordination of Ethics Committee and Regulatory submission in Israel and will coordinate all activities to get investigational sites ready to enroll patients in our clinical trials.

 

Duties include:

  • Preparation, reviewing and coordinating local ethics and regulatory submissions in alignment with global submission strategy
  • Providing local regulatory strategy and advice
  • Acting as a key contact on a country level for all submission related activities and provide oversight for projects
  • Taking ownership of bringing qualified sites to the status of ‘ready to enroll’
  • Draft, review and track contracts, utilizing your legal and commercial acumen.
  • Work with global project teams to provide them with contract and legal support of a high caliber to meet tight deadlines.
  • Maintain knowledge of and understand PPD SOPs, Client SOPs/directives, and current regulatory guidelines as applicable to services provided
  • Additional tasks in line with business and department needs

Qualifications

Qualifications:

·        

  • Bachelor’s degree in a life science subject
  • Regulatory and submission experience and a good knowledge of applicable local requirements.
  • Basic medical/therapeutic area and medical terminology knowledge
  • Excellent communication and organizational skills and a self-motivated, flexible and professional attitude. The ability to handle multiple tasks effectively, often within strict deadlines is essential.
  • English language skills

PPD is equal opportunities employer.


If you are interested in the advertised position, please submit your CV in English.

Apply for this job: Country Approval Specialist, SIA - Israel-147256

Contact Information:

Address:  PPD Cambridge
Granta Park
Great Abington
Cambridge

CB21 6GQ
England
Website:  Visit Our Web Site

Advertising
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.