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Contract Clinical Research Associate (CRA)

Remote: 
Full Remote
Contract: 
Work from: 

Offer summary

Qualifications:

Experience in solo monitoring within a CRO environment., Strong consulting background with a track record of success., Resourceful and curious, with a desire to learn and improve., Technically savvy and able to utilize technology effectively..

Key responsabilities:

  • Collaborate with Site Management and sponsor stakeholders to plan and manage work effectively.
  • Conduct site selection, initiation, monitoring, and close-out visits while maintaining documentation.
  • Establish relationships with sites and administer protocol training as the prime contact.
  • Track submissions, recruitment, and data query resolution to manage project progress.

Peachtree BioResearch Solutions logo
Peachtree BioResearch Solutions Pharmaceuticals SME http://www.peachtreebrs.com/
51 - 200 Employees
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Job description

Peachtree BioResearch Solutions is a specialized full-service CRO providing pharmaceutical and medical device companies with highly specialized teams for their studies.  Formed over 15 years ago by a leadership team experienced in buying CRO services on the sponsor side, our operational teams are highly experienced, bring valuable insight, and create trusting partnerships for our 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. 

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 on some great teams, full-time employees will get:
  • Medical, Dental, Vision, Life, Disability coverage
  • 20 days PTO + 13 Paid Holidays
  • 401(k)

 

Required profile

Experience

Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Adaptability
  • Teamwork
  • Communication
  • Problem Solving

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