Senior Clinical Research Associate (Contract)

Piper Companies is seeking a Senior Clinical Research Associate (Contract) to join a growing Clinical Research Organization (CRO) supporting late-phase clinical studies across the United States. The Senior Clinical Research Associate (Contract) will play a key role in monitoring and site management activities for a Phase III endocrinology study, while partnering with cross-functional teams to ensure high-quality study execution. This is a remote, 12-month contract opportunity (35-40% travel) requiring approximately 30 hours per week initially, with workload decreasing to approximately 20 hours per week after the first several months.

Responsibilities for the Senior Clinical Research Associate (Contract) include:

· Perform remote and on-site monitoring visits to ensure compliance with study protocols, GCP guidelines, and regulatory requirements.

· Support site activation, enrollment oversight, and ongoing site management activities across assigned research centers.

· Review clinical laboratory and pharmacokinetic (PK) data to identify trends, discrepancies, and potential study risks.

· Build strong relationships with investigators and site personnel while providing protocol guidance and training as needed.

· Complete monitoring documentation, track site performance metrics, and communicate study updates to project stakeholders.

Qualifications for the Senior Clinical Research Associate (Contract) include:

· 5+ years of clinical monitoring experience with independent management of investigative sites.

· Experience supporting Phase II and/or Phase III clinical trials within a CRO, biotechnology, or pharmaceutical setting.

· Strong understanding of pharmacokinetic (PK) assessments, laboratory data review, and clinical trial operations.

· Advanced knowledge of GCP, ICH guidelines, FDA regulations, and clinical research best practices.

· Bachelor's degree in Life Sciences, Nursing, Health Sciences, or a related scientific discipline.

Compensation for the Senior Clinical Research Associate (Contract):

Salary Range: $60-$75/hr

Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K

This job opens for applications on 8/21/26. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: clinical research, clinical trials, senior CRA, clinical research associate, CRO, clinical monitoring, site management, pharmacokinetics, PK studies, laboratory data review, GCP, ICH guidelines, FDA regulations, site activation, source data verification, risk-based monitoring, remote monitoring, oncology, endocrinology, phase III clinical trial, phase II clinical trial, biotechnology, pharmaceutical research, protocol compliance, regulatory compliance, CTMS, EDC, investigator relations, clinical operations, monitoring visits, data quality, study startup, trial management, subject enrollment, adverse event review, clinical development, therapeutic area experience, audit readiness, clinical documentation.

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