Note: The job is a remote job and is open to candidates in USA. Piper Companies is seeking a Senior Clinical Research Associate I to join a global organization in the clinical research and life sciences industry. The role supports cardiovascular, CNS, diabetes, and metabolic clinical studies through site monitoring, data and documentation review, site staff training, and compliance oversight.
Responsibilities
- Perform routine and close-out monitoring visits to ensure studies are conducted in alignment with GCP, ICH, and applicable regulations
- Serve as the primary point of contact for assigned research sites, fostering strong relationships and ongoing communication
- Review site data, source documentation, and regulatory files to confirm accuracy, completeness, and protocol adherence
- Provide guidance and training to site staff on protocol requirements, study procedures, and compliance expectations
- Identify, document, and escalate quality or compliance concerns while supporting resolution efforts
Skills
- 1–4 years of onsite clinical monitoring experience, aligned to CRA II or Senior CRA I level
- Experience supporting clinical trials within cardiovascular, CNS, diabetes, or metabolic indications
- Strong working knowledge of GCP, ICH guidelines, and FDA regulatory requirements
- Proficiency with CTMS, EDC systems, and standard clinical trial documentation
- Bachelor's degree in life sciences, nursing, or a related discipline
- Spanish fluency is highly preferred for candidates based in Florida or Puerto Rico
Benefits
- Medical
- Dental
- Vision
- Sick leave if required by law
- 401(k)
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