Clinical Research Associate (CRA II / Senior CRA)

Overview

Remote
54 - 65
Contract - W2
Contract - 06 Month(s)
No Travel Required
Unable to Provide Sponsorship

Skills

Clinical Research Associate (CRA) experience
Site monitoring (SIV
IMV
COV)
GCP / ICH / FDA regulatory knowledge
CRO and vendor coordination
Protocol
ICF
CRF review

Job Details

Immediate need for a talented Clinical Research Associate (CRA II / Senior CRA). This is a 06 months contract opportunity with long-term potential and is located in Santa Monica,CA(Remote). Please review the job description below and contact me ASAP if you are interested.

Job ID: 25-96074

Pay Range: $54 - $65/hour.  Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).

Key Responsibilities:

  • Conduct site qualification, initiation, routine monitoring, and close-out visits
  • Ensure compliance with study protocols, Google Cloud Platform, ICH, FDA/EMEA regulations
  • Review clinical trial documents including protocols, ICFs, CRFs, and monitoring plans
  • Coordinate CROs and vendors with limited supervision
  • Assist in data review, discrepancy resolution, and preparation of safety and study reports
  • Participate in cross-functional meetings with Clinical Operations, Data Management, and Regulatory teams
  • Support training of CRAs and Clinical Project Assistants
  • Identify risks, anticipate obstacles, and implement proactive solutions
  • Support departmental and interdepartmental strategic initiatives

Key Requirements and Technology Experience: 

  • Key Skills;Clinical Research Associate (CRA) experience
  • Site monitoring (SIV, IMV, COV)
  • Google Cloud Platform / ICH / FDA regulatory knowledge
  • CRO and vendor coordination
  • Protocol, ICF, CRF review
  • Strong written and verbal communication
  • Ability to manage multiple studies and priorities
  • Clinical trial operations experience
  • 4 years of CRA or clinical monitoring experience
  • Bachelor’s degree in life sciences OR RN with relevant experience
  • Working knowledge of FDA, EMEA, ICH, and Google Cloud Platform guidelines
  • Strong organizational and problem-solving skills
  • Willingness to travel as required

Our client is a leading Biopharmaceutical Industry and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.

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