Senior Clinical Research Associate

Piper Companies; United States; Sur place; USD 110 000 - 150 000; Plein temps

Avantages offerts par ce poste

Medical coverage

Dental coverage

Vision coverage

Retirement plan

Résumé du poste

Piper Companies is seeking a Senior Clinical Research Associate (CRA) to support a leading organization in the clinical research and biotechnology sector. The Senior CRA will oversee clinical trial sites, ensure adherence to study protocols and regulatory guidelines, and help execute trials across various therapeutic areas including oncology, cardiology, medical technology, and other complex fields.

Responsibilities include on-site and remote monitoring, data quality review, and risk

Qualifications

• 3+ years of CRA experience in CRO, pharmaceutical, biotech, or medical device environments.
• Strong understanding of ICH-GCP guidelines, FDA regulations, and trial operations.
• Excellent communication, organizational, and relationship-management skills.

Responsabilités

• Conduct on-site and remote monitoring visits to ensure compliance with study protocols, GCP, and regulatory requirements.
• Review site performance, source documents, and data quality to maintain trial integrity and participant safety.
• Identify risks and deviations, implementing corrective actions.
• Partner with investigators and cross-functional teams to support enrollment, study execution, and inspection readiness.
• Mentor junior CRAs and provide guidance to sites on quality standards.
• Assist with audit preparation, CAPA activities, and process improvement.

Connaissances

CRA experience

ICH-GCP / FDA regulations

Communication skills

Travel ready

Formation

Bachelor's degree

Description du poste

Piper Companies is seeking a Senior Clinical Research Associate (CRA) to support a leading organization within the clinical research and biotechnology industry. The Senior Clinical Research Associate (CRA) will be responsible for overseeing clinical trial sites, ensuring compliance with study protocols and regulatory guidelines, and supporting successful trial execution across a variety of therapeutic areas, including oncology, cardiology, medical technology, and other complex focuses.

Responsibilities of the Senior Clinical Research Associate (CRA)

• Conduct on-site and remote monitoring visits to ensure compliance with study protocols, GCP guidelines, and specific regulatory requirements.
• Review site performance, source documentation, and data quality to maintain trial integrity and participant safety.
• Identify potential risks, protocol deviations, and operational challenges, implementing corrective actions when necessary.
• Partner with investigators, site staff, and cross-functional teams to support enrollment, study execution, and inspection readiness.
• Mentor junior CRAs and provide guidance to research sites on best practices and quality standards.
• Assist with audit preparation, CAPA activities, and ongoing process improvement initiatives.

Qualifications of the Senior Clinical Research Associate (CRA)

• 3+ years of Clinical Research Associate (CRA) experience within a CRO, pharmaceutical, biotechnology, or medical device environment.
• Bachelor's degree required in a scientific, healthcare, or related discipline.
• Ability to travel approximately 10-12 days per month for on-site monitoring activities.
• Strong understanding of ICH-GCP guidelines, FDA regulations, and clinical trial operations.
• Experience monitoring oncology studies preferred; candidates with experience in other complex therapeutic areas will also be considered.
• Excellent communication, organizational, and relationship-management skills.

Compensation for the Senior Clinical Research Associate (CRA) includes

• Salary range: $110,000 - $150,000 depending on experience
• Comprehensive benefits package including medical, dental, vision, and retirement plans
• Location: West/West Coast based

This job opens for applications on 10/26/2026. Applications for this job will be accepted for at least 30 days from the posting date.

SEO Keywords

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