Clinical Research Associate; CRA Raleigh, NC

Clinical Research Associate (CRA) job at Peachtree Bio Research Solutions. Raleigh, NC.

Peachtree Bio Research Solutions, a Julius Clinical Company, is a global specialized full-service CRO providing highly specialized study operations teams for pharmaceutical, biotech, and medical device companies. Formed over 15 years ago by a pharma leadership team experienced in buying CRO services with the purpose of creating trusting partnerships with sponsor clients - no matter their budget. We do this by investing in people who thrive in an environment where their experience and contributions can be felt throughout the organization.

It's an exciting time as we expand our global reach, while still offering a personalized approach to sponsors and delivering incredible value.

Peachtree Bioresearch Solutions is a fast growing, full-service Clinical Research Organization with expertise in CNS and other therapeutic areas. We create strong, consultative relationships with sponsor clients and we're looking to add CRAs who are dedicated, want to make an impact, and enjoy having visibility across the entire project beyond their monitoring role.

As a small/mid CRO, we focus on building great teams where all ops functions can provide a high level of service. You can see the impact you make, and get recognized for it. It's also fun working with others who are very good at what they do.

Responsibilities:

• Work closely with the Site Management team and sponsor stakeholders so you can plan and manage your work most effectively
• Perform site selection, initiation, monitoring and close-out visits, plus maintain the appropriate documentation
• Establish relationships with sites while administering 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

Qualifications:

• Bachelor's 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%. Sometimes it's hectic. Sometimes it's not. We do a good job trying to manage it.
• 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

In addition to working with great people on high performing teams, full-time employees receive:

• Medical, Dental, Vision, Life, Disability coverage
• 20 days PTO + PTO rollover + 13 paid holidays
• 401(k)