Entry Level Clinical Research Associate - 105184 Job at Medix™, Baton Rouge, LA

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  • Medix™
  • Baton Rouge, LA

Job Description

Are you a seasoned Clinical Research Coordinator ready to step into the world of monitoring? We’re seeking an enthusiastic and detail-oriented Entry-Level CRA to support a pivotal HIV device trial launching this summer.

This is a hybrid, contract-based role specifically designed for someone with strong site-level experience—ideally a Senior CRC —who's eager to learn the ropes of monitoring and grow into a CRA position. You'll receive hands-on training and mentorship as you begin to conduct site visits and develop monitoring skills.

Please note: While this is an entry-level CRA role, there will still be some Clinical Research Coordinator responsibilities involved, so strong site experience is essential. The position will average 30 hours in-office and 10 hours remote per week.

Key Responsibilities

  • Assist with site monitoring visits under supervision, including initiation, routine, and close-out visits
  • Support investigational sites with compliance, protocol adherence, and data quality
  • Help review regulatory documents, source data, and case report forms (CRFs)
  • Act as a liaison between the sponsor and clinical sites to ensure clear communication
  • Participate in training activities to build a strong foundation in GCP and monitoring best practices
  • Maintain accurate trial documentation and reporting
  • Perform some on-site CRC duties as needed to support trial activities

What We’re Looking For

  • 3+ years of experience as a Clinical Research Coordinator, preferably with senior-level responsibilities
  • Hands-on experience working on diagnostic device trials (required)
  • Familiarity with regulatory documents, protocol implementation, and site coordination
  • Strong communication and organizational skills
  • Comfortable with limited travel for monitoring visits
  • Eager to transition into a CRA role and open to learning
  • Prior experience in HIV research or medical device trials is a plus (not required)
  • Must be based in Baton Rouge – this is a hybrid role with some in-person responsibilities

Why This Role?

  • Step into a CRA career path with mentorship and training
  • Get experience in the high-impact field of HIV device research
  • Work in a supportive, learning-focused environment
  • Make a real contribution to a meaningful trial
  • Enjoy the flexibility of a hybrid schedule while gaining monitoring experience

Job Tags

Contract work, Summer work, Remote job,

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