Clinical Research Associate

Full Time
Alameda, CA 94501
$50 - $59 an hour
Posted Just posted
Job description

PLEASE NOTE THAT THE CANDIDATE WILL START AS SOON AS SELECTED AND HAS CLEARED ONBOARDING.

Local Candidates needed

POSITION IS 6 MONTHS FROM START DATE WITH POSSIBLE EXTENSIONS.

ONSITE ONLY IN ALAMEDA UNLESS TRAVELING AND UP TO 50% TRAVEL WHEN NEEDED BUT MAY NOT BE IMMEDIATELY.

Requesting that candidate is local and work on-site in Alameda, CA, 5 days a week when not traveling.

  • Bachelor’s degree REUIRED WITH A PREFERANCE IN Biological Sciences which fit best BUT “Life Sciences” degrees will also be considered
  • Minimum of 3 to 5 years of clinical exp. within industry
  • Specifically looking for monitoring exp. on the sponsor side
  • Will be supporting a multi-site study
  • Exp. with site selection
  • Will be doing monitoring visits
  • Medical device exp. of at least 1 year
  • Exp. coordinating site initialization and site close
  • Familiar with IRB (Institution Review Board) submission
  • ICF (informed consent forms) revision exp.
  • Exp. editing/revising CRF “case report forms”
  • Familiarity with data cleaning and database process (Queries)
  • Basic MS Office with Outlook, Project, PowerPoint and Excel
  • Training PI staff
  • HCI Guidelines
  • “Viva” exp. is for electronic filing is preferred
  • Device Trial Study where will be tracking adverse events
  • Take ownership and coordinate shipping out devices, the return of devices and device accountability

Question ~ Medical device exp. needed or is Pharma exp. ok? Answer = want 1 year medical device exp.

Question ~ Is the travel domestic or international? Answer = domestic only.

Job Type: Contract

Salary: $50.00 - $59.00 per hour

Schedule:

  • 8 hour shift
  • Day shift

Ability to commute/relocate:

  • Alameda, CA 94501: Reliably commute or planning to relocate before starting work (Required)

Education:

  • Bachelor's (Preferred)

Experience:

  • site monitoring: 5 years (Preferred)
  • site visit and site close out: 5 years (Preferred)
  • editing/revising CRF “case report forms”: 4 years (Preferred)
  • Familiar with IRB (Institution Review Board) submission: 4 years (Preferred)
  • pharma or medical device industry: 1 year (Preferred)

Work Location: One location

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