Clinical Research Associate (CRA)

Piper Companies; L'Âge; Hybride; EUR 61 000 - 75 000; Plein temps

Résumé du poste

A leading clinical research organization is looking for an experienced Clinical Research Associate (CRA) to join the team. The CRA will play a key role in monitoring and managing clinical trials for a top pharmaceutical client, ensuring compliance with regulations and maintaining data integrity. Responsibilities include conducting site visits, training site staff, and reporting adverse events. The ideal candidate has a related Bachelor’s degree and at least 2 years of on-site CRA experience. Comprehensive benefits and a salary range of $100,000 - $120,000 CAD are offered.

Prestations

Comprehensive Benefits including medical, dental, and vision

401K

Paid Time Off

Sick Leave

Holidays

Qualifications

• At least 2 years of experience as an On-site CRA.
• Comfortable with up to 70% travel (2-3 days per week).
• Strong understanding of regulatory requirements.
• Must be comfortable handling RECIST and CTCAE inquiries.

Responsabilités

• Monitor clinical trials for compliance with protocols and regulations.
• Conduct site visits including pre-study and monitoring.
• Review CRFs and source documents for accuracy.
• Ensure timely reporting of adverse events.
• Provide training to site staff on protocols.
• Maintain communication with study sites and investigators.

Connaissances

Clinical Trial Processes

Interpersonal Skills

Organizational Skills

Communication Skills

Time Management

Formation

Bachelor’s degree in a related field

Description du poste

Piper Companies is seeking an experienced Clinical Research Associate (CRA) to join our client’s team. This opportunity is with an industry‑leading Clinical Research organization supporting one of the top pharmaceutical companies in the world. The CRA will play a critical role in monitoring and managing clinical trials, ensuring compliance with regulatory requirements, and maintaining high standards of data integrity and patient safety.

Locations for the Clinical Research Associate: United States (PST, MST, CST) and Canada

Responsibilities for the Clinical Research Associate:

• Monitor clinical trials to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
• Conduct site visits, including pre‑study, initiation, monitoring, and close‑out visits.
• Review and verify case report forms (CRFs) and source documents for accuracy and completeness.
• Ensure timely and accurate reporting of adverse events and protocol deviations.
• Provide training and support to site staff on study protocols, procedures, and regulatory requirements.
• Maintain effective communication with study sites, investigators, and other stakeholders.
• Assist in the preparation and review of study‑related documentation, including informed consent forms, study manuals, and monitoring plans.
• Participate in study team meetings and provide updates on site status and study progress.

Qualifications for the Clinical Research Associate:

• At least 2 years of experience as an On‑site CRA.
• Comfortable with up to 70% travel (2‑3 days per week).
• Must have a valid driver’s license.
• Must be comfortable handling questions regarding RECIST (Response Evaluation Criteria in Solid Tumors) and CTCAE (Common Terminology Criteria for Adverse Events).
• Strong understanding of clinical trial processes and regulatory requirements.
• Excellent organizational and time management skills.
• Strong communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Bachelor’s degree in a related field (e.g., life sciences, nursing, pharmacy).

Compensation/Benefits for the Clinical Research Associate:

• Salary: $100,000 - $120,000 CAD
• Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays

This job opens for applications on 12/11/2025. Applications for this job will be accepted for at least 30 days from the posting date.

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