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Senior Site Manager (CRA) - Tel Aviv - Global Pharma Leader

Business Type: Clinical Research Organisation
Job Type: Clinical Research Associate (CRA)
Job Level: Management
Position: Contract
Location: Israel
Reference: PP 294980 5
Closing Date: 29/10/21
Job Details:

Senior Site Manager (CRA) - Tel Aviv

An international medical device/pharma company is looking for Senior Site Manager (CRA) to join their international team. Our client Provides global, regional or complex local management of clinical research activity in multiple countries worldwide! Creating pioneering solutions and pushing the boundaries of what''s next in talent, they help you to not only reach and exceed your goals but to build your future.

Work together with an international team - Expand your network internationally - will help you in your future career and it will be interesting to learn from other cultures as well as an excellent opportunity to build your career within a world leader in pharmaceutical industry.

Working with us, you can reach your full potential and make a concrete contribution to global healthcare. Our client combines decades of industry experience with the latest technology and analytics, to deliver trailblazing products and solutions that help customers to outpace the competition.

Location: Israel, 2 days of site travel
Contract: 1+ years, multiple extensions.

Some Responsibilities include:

  • Site Management services provides Trial Co-ordination and Site Management services as primary point of contact between the sponsor and the investigational site.
  • Manage 8-10 sites across 3 studies in the area assigned.
  • Focus on early stages Phase I, II and III
  • Services/deliverables include ensuring trial sites are inspection ready, through compliance with the clinical research protocol, company''s Standard Operating Procedures (SOP), International Conference on Harmonization for Good Clinical Practice (ICH-GCP) and applicable regulations from start-up through data-base lock.
  • Further, services/deliverables will include pre-trial assessment, site selection, subject recruitment and retention planning, site initiation, monitoring and close-out.
  • Partners with the Clinical Trial Assistant (CTA)/Investigator Document Assistant (IDA), Local Trial Manager (LTM) and Central Trial Manager (CTM)/Global Trial Manager (GTM) to ensure overall site management while performing trial related activities for assigned protocols.


  • BA/BS degree/Degree in a health or science related field or equivalent industry experience
  • Advanced: 3 to 5+ years of clinical trial monitoring experience.
  • 4 years of relevant experience ( CRA or similar)
  • Experience with early stages trials Phase II and III or similar
  • Available to travel 30-40%
  • Specific therapeutic area experience depending on the services need.
  • Strong working knowledge of ICH GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines.
  • Strong IT skills in appropriate software and company systems.
  • Willingness to occasional travel with overnight stay away from home according to business needs.
  • Proficient in speaking and writing in English and the country language where services will be provided. Effective communication skills, oral and written.
  • Experience with monitoring and site management of complex Early Phase of clinical development, as applicable.


  • Build your career within a world leader in pharmaceutical industry
  • Attractive benefit package
  • Diverse job activities and opportunity to develop as a Site Manager
  • Join a diverse team, who all work together to make a concrete contribution to global healthcare

Apply and send your CV to or give me a call on Phone: +44 207 940 2105 Internal Extension: 3363. My name is Patrick Powell, I am a specialist Head-Hunter working for NonStop Consulting, which is one of the largest and fastest-growing specialised life sciences recruitment companies in Europe.

We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Luxembourg, Switzerland, Romania, the US, and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.

Posted: 22/10/2021 | NPJ Ref: 286948
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