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Clinical Research Associate
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08-01
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We are seeking full-time clinical research associates (CRA) to join our clinical operations team. This Western Canada based home position requires up to 70% of travel, including overnight stays.
The CRA will act as the primary contact with the investigative sites and be responsible for the oversight of all aspects of Phase I to IV clinical research projects at the site level, assuring investigative site adherence to Good Clinical Practice (GCP) guidelines and compliance to Allphase and client study protocols.
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Clinical Research Associate
Duties:
- Perform site selection, site initiation, interim monitoring and site closure visits
- Coordinate investigator and study meetings, including preparation and presentation of information and training investigative site staff on protocol, study conduct, GCP Guidelines & regulatory requirements
- Document clinical trial progress to ensure completeness of documentation and data collection, management of supplies and resources in adherence with the project timelines, budgets and quality standards
- Complete investigative site file reconciliation; request new or updated site-related essential and non-essential documents and analyze for accuracy, content, consistency and compliance
- Monitor clinical trial progress for compliance with regulatory and budgetary requirements
- Complete visit or trip reports at the conclusion of each monitoring visit according to company and sponsor standard operating procedures (SOPs)
- Interact with internal groups including data management, quality assurance and business development during clinical study lifecycle
- Assist the clinical study team with the development of clinical protocols, case report forms and clinical study reports
- Fulfill other duties as required
Qualifications:
- Degree in life or medical sciences such as nursing, pharmacy or basic sciences. Advanced degree considered an asset.
- A minimum of two (2) years of experience in clinical research with primary site monitoring responsibilities
- Therapeutic experience in Oncology
- Valid driver’s license and passport required
- Must be able to travel up to 70% of the time
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Resumes are retained for a period of six (6) months. Should you wish that
Allphase not retain your application, please specify in your cover letter.
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Allphase Clinical Research is an equal opportunity employer. While we
appreciate all applications received, only those considered for an
interview will be acknowledged. No telephone calls, please.
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