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Job Details

Start-up and Regulatory Specialist (Israel)

Company: ProClinical Ltd
Location: Israel
Reference: CR.TS.10851
Closing Date: 24 Feb 17
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

An exciting clinical regulatory job has emerged as a Start Up and Regulatory Specialist at one of the world's largest global CROs. This contract research organisation provides support services to many of the biggest names in pharmaceuticals, biotech, medical devices and health care, and has helped to commercialise many leading therapies. This position will be based at their site in Israel. ...

Requirements:

An exciting clinical regulatory job has emerged as a Start Up and Regulatory Specialist at one of the world's largest global CROs. This contract research organisation provides support services to many of the biggest names in pharmaceuticals, biotech, medical devices and health care, and has helped to commercialise many leading therapies. This position will be based at their site in Israel.

Job Role:

  • Under direction of line manager, support the delivery of activities as determined by the appropriate country, regional lead or global lead. May conduct specific tasks under guidance of senior staff. Responsibilities may include all or some of the activities listed at any one time.

Job Responsibilities:

  • Assist the team in the preparation, handling, distribution, filing and archiving of documentation according to the scope of work and standard operating procedures
  • Review documents for completeness, consistency and accuracy, under guidance of senior staff
  • Prepare client deliverable documents using appropriate tools and may draft text for straightforward documents, under guidance of senior staff
  • Assist with completion of relevant Clinical Trial Management System (CTMS) fields, databases, tracking tools, timelines and project plans with project specific information
  • Provide support for administrative tasks, e.g. meeting coordination, minute taking, travel arrangements, faxing, copying, couriers
  • Interact with internal and external clients, under guidance of senior staff
  • May perform IP release activities on small, straightforward projects or support reviews for larger projects

Job Requirements:

  • CRA course, with profound knowledge in ICH-GCP
  • At least few months experience as Study Coordinator
  • Experience with Ethic Committee submission preparations
  • Individual learning ability, ability to work independently and also within a team
  • Very high level of English and Hebrew
  • Excellent interpersonal skills

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Theodora Savlovschi-Wicks on +44 203 7520 314 or upload your CV on our website www.proclinical.com.
A full job description is available on request.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Apply for this job: Start-up and Regulatory Specialist (Israel)

Contact Information:

Address:  ProClinical Ltd
Eldon House Eldon Street London
EC2M 7LS
England
Tel:  0800 988 4437
Fax:  +44 (0)207 834 9470
Website:  Visit Our Web Site

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