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Clinical Research Associate (CRA)

Canada, Canada

Piper Companies Logo

Job Id:
139017

Job Category:

Job Location:
Canada, Canada

Security Clearance:
None

Business Unit:
Piper Companies

Division:
Piper Enterprise Solutions

Position Owner:
Anne Green

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
  • Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays


This job opens for applications on 3/21/2025. Applications for this job will be accepted for at least 30 days from the posting date.


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