Senior Clinical Research Associate

Upsilon Global - Streamlining Clinical Trials

Upsilon Global is seeking a freelance SCRA based on the East Coast to support sites in Atlanta, GA, for an addiction / abuse liability study due to launch early February. This will be an 0.5-0.7 FTE study, possibly increasing to 0.8-0.9 FTE depending on enrollment.

This CRO partner specializes in early-phase/translational trials, meaning a strong background in phase I/II studies as well as a keen scientific focus for clinical monitoring is essential.

Experience in abuse liability is essential, with experience in either opioid abuse or tobacco addiction being highly advantageous.

• Position:
  Freelance SCRA
• Employment: 1099 contract
• FTE: 0.5-0.7 fte (possibly up to 0.8-0.9 fte)
• Indication:
  Abuse liability (opioids / tobacco)
• Start Date:
  
  February 2026
• Travel:
  Single site in Atlanta, GA
• Location:
  
  Greater Atlanta area preferable, although anyone within reasonable distance considered

• Conduct on-site visits, monitoring and assessment of clinical trial site, ensuring adherence to study protocols, Good Clinical Practice (GCP) guidelines, and applicable regulatory requirements.
• Perform source document verification, data collection, and accurate recording of study data, ensuring data integrity and compliance.
• Collaborate with site investigators, site staff, and study team members to ensure successful execution of clinical trials.
• Assist in the development and review of study documents, including protocols, informed consent forms, and case report forms.
• Maintain effective communication with study site, sponsors, and other stakeholders to provide timely updates, address queries, and resolve issues.
• Monitor subject safety, reporting adverse events, and ensuring appropriate follow-up actions are taken.
• Contribute to the preparation and coordination of study initiation, monitoring, and close-out activities.
• Assist in the preparation and participation in regulatory inspections and audits as necessary.
• Stay updated with current regulations, guidelines, and industry trends related to clinical research in translational/early-phase trials.

• 5+ years independent monitoring experience
• Experience in abuse liability essential
• A strong background in early-phase / phase I/II trials
• In-depth knowledge of U.S. regulatory requirements and clinical trial processes.
• Strong organizational and communication skills, with the ability to manage multiple priorities.
• Ability to work independently, demonstrating initiative, attention to detail, and problem-solving skills
• Willingness to travel across the East Coast

For more information, please apply via the link or contact a