Clinical Research Associate (Cra)

Peachtree BioResearch Solutions is a specialized full-service CRO that "thinks like a sponsor". Formed almost 15 years ago by a leadership team experienced in buying CRO service while at a global pharma, our operational teams are highly experienced and bring valuable insight for our small sponsor clients - no matter their budget. We do this by investing in people who thrive in an environment where their experience and insight can be leveraged beyond their main functional area. This is a great environment for people who want to do more.

Peachtree Bioresearch Solutions is a fast growing, full-service Clinical Research Organization with expertise in CNS and rare disease. We create strong, consultative relationships with sponsor clients. We're looking to grow our Site Management team with a west coast based CRA. To be successful in this role, CRAs must be business-minded and willing to consistently go above and beyond.

This is a great opportunity for someone who has some clinical research experience but is looking learn more. You'll be mentored by industry experts with a proven track record of success. At Peachtree, great work is recognized and rewarded. If you're looking to contribute in a meaningful way and do more than just 'check boxes', this is the role for you.

Responsibilities:

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

Qualifications:

• Be resourceful and curious - you figure out problems and think about the business beyond the task at hand.
• Experience working in a CTMS and EDC system
• Highly proficient with business software (MS365)
• Experience with CNS, rare disease and/or oncology studies preferred
• Excellent written and verbal communication and presentation skills
• Bachelor's degree
• 1-5 years of experience working on clinical trials (CRO or Sponsor) as either a coordinator or CRA I
• Leadership traits and attitude
• Excellent organizational and critical thinking skills
• Willing and able to travel up to 65%
• A team player who elevates others
• Nursing experience ideal

In addition to working on some great teams, full-time employees will get:

• Medical, Dental, Vision coverage (Company contributes significantly to premiums)
• 100% employer matching 401(k)
• 20 days PTO + 13 Paid Holidays
• Short & Long-term disability benefits