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

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