Clinical Trials Associate - Santa Monica, United States - Infotree Global Solutions

Infotree Global Solutions
Infotree Global Solutions
Verified Company
Santa Monica, United States

1 week ago

Mark Lane

Posted by:

Mark Lane

beBee recruiter
Description
Provides administrative assistance in site selection, study implementation and ongoing coordination of study sites, either directly or via CROs.


Monitors fairly routine study sites, performing routine data collection, source data verification, and review of routine regulatory documents/files in compliance with protocol, regulatory requirements, SOPs, and Monitoring Plan, as required.


Under supervision may assist in review of protocols, informed consents, and case report forms, monitoring plans, abstracts, presentations, manuscripts and clinical study reports.

Assists in preparation of safety, interim and final study reports, including resolving data discrepancies.

Travel is required.

Excellent verbal, written, interpersonal and presentation skills are required. Must be familiar with routine medical/scientific terminology.

Must be familiar with Word, PowerPoint, and Excel.

Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable.

Must be able to participate in departmental or interdepartmental strategic initiative under general supervision.

Must be able to contribute to SOP development.


Job Type:
Contract


Pay:
$ $40.00 per hour


Schedule:

  • 8 hour shift
  • Day shift
  • Monday to Friday

Experience:


  • Site monitoring: 2 years (required)

Ability to Commute:

  • Santa Monica, CA required)

Work Location:
In person
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