Job Description
At Target RWE, our mission is driven by a deep commitment to people—whether it’s the patients we serve, the partners we collaborate with, or the dedicated team members who power our work. As a purpose-driven organization, we leverage real-world data to advance clinical research and inform better healthcare decisions. We foster a collaborative environment where every voice is heard, every idea has impact, and every contribution helps improve lives. If you're seeking a place where your work truly matters, join us to advance science.
We are seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to support observational and prospective studies. The CRA will be responsible for site management and data monitoring of assigned clinical sites, ensuring compliance with Good Clinical Practices (GCP) and Standard Operating Procedures (SOP). This role requires strong organizational skills, independent judgment, and the ability to collaborate with cross-functional teams to ensure the success of clinical research studies.
What You'll Do
Site Selection & Initiation:
Site Management & Monitoring:
Study Support & Compliance:
Travel & Additional Responsibilities:
What You'll Bring
If you are ready to be part of a team where your work truly matters - where your expertise is valued, your growth is supported, and your contributions help shape the future of healthcare, Target RWE is the place for you. We’re building something meaningful together, and we’d love for you to be a part of it.
Total Rewards
The salary estimated for this position is $62,000-92,000 per year. Compensation will vary depending on job-related knowledge, skills and experience. Actual compensation will be confirmed in writing at the time of offer.
What we offer you
Hybrid + remote work environment
Comprehensive health, dental, and vision for you and your family
401(k) with company match
Generous PTO and company holidays
Paid parental leave
Hybrid role: 1 day per week in office located in Raleigh/Durham, NC or Dallas, TX
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