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Site Management Associate - Boston-based candidates preferred!

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About the role

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The Site Management Associate I/II  is responsible for managing, implementing and monitoring clinical studies in a team setting. 
 
Responsibilities include, but are not limited to:
  • Identifying, training/initiating and closing out study sites
  • Conducts and completes remote site managmenet activities, with support as needed, accorgind to the Site Managmennt Plan.
  • Manage study sites and required protocols, amendments and deviations.
  • Assure data is reported accurately and timeline are maintained.
  • Serves as the primary contact for sites and investigatos participating in studies.
  • Maintains, reviews, and ensures adequacy of information and data contained in site management reports, tracking systems (CTMS or others) and other site management documents.
  • Review drug storage and drug accountability procedures in accordance with applicable SOPs.
Educational Requirements:
  • Bachelor’s degree or local equivalent in medicine, science or related discipline.
 
Requirements:
  • Minimum of one year of relevant experience in a health care or research environment strongly preferred.
  • Ability to review and evaluate clinical data
  • Strong oral and written communication skills
  • This position may require travel up to 25% of the time. 
ICON Plc is an equal opportunity employer.  All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
 
For more information about personal rights under Equal Employment Opportunity, visit:
 
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