Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Apply Offsite

Clinical Research Coordinator

Job

Society of Clinical Research Associates (SOCRA)

Baton Rouge, LA (In Person)

$85,000 Salary, Full-Time

Posted 3 weeks ago (Updated 5 days ago) • Actively hiring

Expires 7/23/2026

Review key factors to help you decide if the role fits your goals.
How is this calculated?
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
82
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Job Details Title:
Clinical Research Coordinator
Company:
Vitreoretinal Institute
Location:
Vitreoretinal Institute AMC
  • Baton Rouge, LA Vitreoretinal Institute AMC is a growing, multi-physician retina practice launching a dedicated clinical trials program focused on vitreoretinal disease and uveitis.
We are seeking an experienced Clinical Research Coordinator (CRC) to build and manage our research operations. This is a unique opportunity to help build a program from the ground up with strong physician support, an established patient base, and a clear path to growth. ⸻
Key Responsibilities:
Study Coordination:
  • Manage all aspects of clinical trials from startup to closeout
  • Coordinate patient visits per protocol (screening, baseline, follow-ups)
  • Ensure compliance with
GCP, FDA
regulations, and protocol requirements ⸻
Patient Management:
  • Identify and pre-screen eligible patients from clinic schedules and EMR
  • Coordinate informed consent process
  • Serve as primary point of contact for study participants ⸻
Regulatory & Documentation:
  • Prepare and maintain regulatory binders
  • Submit documents to IRBs (central IRB preferred)
  • Track adverse events and protocol deviations
  • Ensure audit readiness at all times ⸻
Sponsor & CRO Interaction:
  • Act as liaison with sponsors, monitors, and CROs
  • Participate in site initiation visits (SIVs), monitoring visits, and audits
  • Manage queries and data entry (EDC systems) ⸻ Operational Development (IMPORTANT):
  • Help develop SOPs and workflows for a new research program
  • Assist in building scalable processes for future growth
  • Contribute to site feasibility assessments ⸻
Qualifications:
Required:
  • 2+ years experience as a Clinical Research Coordinator
  • Experience managing clinical trials independently
  • Strong knowledge of: 1. GCP (Good Clinical Practice) 2. Informed consent process 3. Regulatory requirements 4. Excellent organizational and communication skills Preferred (Strongly):
  • Ophthalmology or retina trial experience
  • Experience with: 1.
OCT imaging 2. Visual acuity testing 3. Injection-based studies 4. Experience working in a private practice setting ⸻
Compensation & Benefits:
  • Salary:
    $75,000
  • $95,000+ (based on experience)
  • Performance-based bonus potential
  • Health benefits
  • Paid time off
  • Opportunity for career growth as the research division expands ⸻
What Makes This Role Unique:
  • Build a research program from day one
  • Work directly with retina specialists
  • Access to a large, established patient population
  • Strong institutional commitment to research growth To apply for this position or to learn more, please contact "retinaresume@gmail.
com".
SOCRA Exp:
7/2/2026