Note: The job is a remote job and is open to candidates in USA. Piper Companies is actively seeking a Clinical Research Associate to join a well‑established, full‑service CRO supporting global clinical programs. This position is fully remote and requires 60–80% travel, playing a key role in ensuring studies are conducted in compliance with protocols, regulatory requirements, and timelines across multiple therapeutic areas.
Responsibilities
- Monitor and oversee clinical trial activities across Phase I–IV studies in alignment with study protocols and regulatory standards
- Serve as the primary point of contact between sponsors and investigative sites
- Conduct onsite and remote monitoring visits, ensuring data integrity and patient safety
- Review and maintain study documentation and perform data evaluation to ensure accuracy and compliance
- Collaborate cross‑functionally to support study timelines, deliverables, and overall program execution
- Identify and escalate risks, deviations, and issues, supporting resolution and compliance efforts
Skills
- 1+ years of on-site clinical monitoring experience
- Experience working within a CRO or supporting full-service clinical programs
- Strong knowledge of FDA regulations, ICH‑GCP guidelines, and clinical trial processes
- Bachelor's degree in Life Sciences or a related field
- Ability to travel 60–80% regionally
- Therapeutic experience in Cardiovascular, CNS, and/or Diabetes/GLP‑1 studies
Benefits
- Medical
- Dental
- Vision
- 401(k)
- PTO
- Additional benefits
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