Remote CRA for Cardiovascular & CNS Trials

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.

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.