Clinical Research Associate - 173725

Piper Companies; United States; Remote; USD 100,000 - 125,000; Full time

Benefits offered by this job

Health, Vision, Dental

PTO and paid holidays

Remote with travel reimbursement

Job summary

Piper Companies is seeking a Clinical Research Associate to support a growing client in the pharmaceutical industry in the United States. The Clinical Research Associate role is fully remote with regional travel required to clinical trial sites.

Ideal candidates have 3+ years of CRA experience with exposure to cardiovascular, CNS, diabetes, and GLP-1 trials, and a strong knowledge of ICH-GCP and FDA regulations.

Qualifications

• 3+ years of CRA experience with exposure to cardiovascular, CNS, diabetes, and GLP-1 trials.
• Demonstrated ability to independently monitor studies and manage multiple sites.
• In-depth knowledge of ICH-GCP guidelines, FDA regulations, and clinical trial processes.
• Prior experience working with sponsors or CROs in a fast-paced environment.
• Ability to travel approximately 25–40% as needed.

Responsibilities

• Conduct routine and complex monitoring visits to ensure study compliance with protocols, regulatory requirements, and GCP standards.
• Manage site performance by reviewing enrollment progress, data accuracy, and protocol adherence across multiple studies.
• Act as a key point of contact for investigative sites, providing ongoing support and resolving study-related issues.
• Evaluate clinical data and documentation to ensure patient safety and data integrity throughout the trial lifecycle.
• Collaborate with cross-functional teams and sponsors to drive study milestones and maintain timelines.

Skills

ICH-GCP knowledge

FDA regulations

Study monitoring

Travel readiness

Job description

Piper Companies is seeking a Clinical Research Associate to support a growing client in the pharmaceutical industry in the United States. The Clinical Research Associate role is fully remote with regional travel required to clinical trial sites. The Clinical Research Associate role is ideal for an experienced professional with strong expertise across non-oncology therapeutic areas including Cardiovascular, CNS, Diabetes, and GLP-1 studies.

Responsibilities of the Clinical Research Associate include:

• Conduct routine and complex monitoring visits to ensure study compliance with protocols, regulatory requirements, and GCP standards
• Manage site performance by reviewing enrollment progress, data accuracy, and protocol adherence across multiple studies
• Act as a key point of contact for investigative sites, providing ongoing support and resolving study-related issues
• Evaluate clinical data and documentation to ensure patient safety and data integrity throughout the trial lifecycle
• Collaborate with cross-functional teams and sponsors to drive study milestones and maintain timelines

Requirements of the Clinical Research Associate include:

• 3+ years of CRA experience with strong exposure to Cardiovascular, CNS, Diabetes, and GLP-1 trials
• Demonstrated ability to independently monitor studies and manage multiple sites simultaneously
• In-depth knowledge of ICH-GCP guidelines, FDA regulations, and clinical trial processes
• Prior experience working directly with sponsors or CROs in a fast-paced environment
• Ability to travel approximately 25–40% as needed

Compensation for the Clinical Research Associate include:

• $100,000 – $125,000 annually
• Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.
• Remote work flexibility with travel reimbursement
• This job opens for applications on 918/2026. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: Clinical Research Associate, CRA, Cardiovascular, CNS, Diabetes, GLP-1, Clinical Trials, Remote, Monitoring

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