Remote CRA – Multispecialty Cardiovascular/CNS Trials

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

Benefits offered by this job

Remote work

Travel reimbursement

Comprehensive benefits

Job summary

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

Ideal for an experienced professional with strong exposure to Cardiovascular, CNS, Diabetes, and GLP-1 studies, the CRA will monitor sites, ensure compliance with ICH-GCP and FDA regulations, and collaborate with sponsors to meet milestones.

Qualifications

• 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.

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

Cardiovascular trials

CNS trials

Diabetes trials

GLP-1 studies

ICH-GCP knowledge

FDA regulations

Job description

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

Ideal for an experienced professional with strong exposure to Cardiovascular, CNS, Diabetes, and GLP-1 studies, the CRA will monitor sites, ensure compliance with ICH-GCP and FDA regulations, and collaborate with sponsors to meet milestones.