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Contract Clinical Research Associate (CRA)

Contract Clinical Research Associate (CRA)

Peachtree BioResearch SolutionsRaleigh, NC, US
1 day ago
Job type
  • Full-time
Job description

Job Description

Job Description

Peachtree BioResearch 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.

We're looking to add a Contract Clinical Research Associates (CRA) who is open to partial FTE. This role will be remote - US Only. Our CRAs value relationship building, are business minded, and want to work with other high performers on winning teams. CRAs at Peachtree are highly consultative with superior communication skills that bring knowledge / value to each project.

Some of the responsibilities :

  • Work closely with 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
  • As prime contact, you'll establish relationships with sites while administering protocol and related study training
  • Work with dynamic Data Management team and sites to ensure all queries are resolved
  • Complete all reports and follow up in a timely manner
  • Manage progress by tracking submissions, recruitment, case report form (CRF) completion, and data query resolution
  • Contribute to process efficiencies and provide input when gaps are identified

Qualifications :

  • solo monitoring experience within a CRO environment
  • Incorporated with a track record of consulting
  • Be resourceful and curious - always looking to learn and improve
  • A team player who elevates others
  • high sense of urgency and extremely positive attitude
  • Technically savvy - not afraid to use technology to become more efficient
  • CNS, rare disease, oncology study experience is ideal but not required.
  • EMR and critical care experience preferred
  • 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)
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    Clinical Research Associate • Raleigh, NC, US

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