
Biotechnology • Pharmaceuticals • Science
Peachtree BioResearch Solutions is a full-service Clinical Research Organization based in the United States. The company focuses on providing a solutions-based approach to small and mid-size sponsors by offering a range of services including site management, clinical monitoring, study feasibility, data management, biostatistics, project management, quality assurance, and medical writing and monitoring. Peachtree emphasizes flexibility, scalability, and reliability in its services, with experienced staff in biostatistics, data integrity, and medical trial management.
51 - 200 employees
Founded 2013
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
September 24

Biotechnology • Pharmaceuticals • Science
Peachtree BioResearch Solutions is a full-service Clinical Research Organization based in the United States. The company focuses on providing a solutions-based approach to small and mid-size sponsors by offering a range of services including site management, clinical monitoring, study feasibility, data management, biostatistics, project management, quality assurance, and medical writing and monitoring. Peachtree emphasizes flexibility, scalability, and reliability in its services, with experienced staff in biostatistics, data integrity, and medical trial management.
51 - 200 employees
Founded 2013
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
• Work closely with the Site Management team and sponsor stakeholders to plan and manage work effectively • Perform site selection, initiation, monitoring and close-out visits, and maintain appropriate documentation • Establish relationships with sites and administer protocol and related study training • Work with Peachtree's Data Management team and sites to ensure all queries are resolved • Complete all reports and follow up items in a timely manner • Work with project leadership to customize solutions that bring value to the sponsor • Provide visibility across the entire project beyond monitoring role
• Bachelors degree • 1-5 years of experience working on clinical trials (CRO or Sponsor) with at least a year of site monitoring • Experience on CNS or neuro studies highly desirable • Willing to travel 65% (may be hectic at times) • Highly proficient with business software (MS365) • Experience working in a CTMS and EDC system • Excellent organizational and critical thinking skills • Excellent written and verbal communication and presentation skills • Be resourceful and curious - you figure out problems and think about the business beyond the task at hand. • A team player who elevates others • Leadership traits and attitude
• Medical, Dental, Vision, Life, Disability coverage • 20 days PTO + PTO rollover + 13 paid holidays • 401(k)
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