Senior Clinical Research Associate job opportunity at Jobgether.

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Date2026-05-12 bot
Jobgether Senior Clinical Research Associate
Experience: 5-years
Pattern: Full-time
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loacation Canada, Canada
loacation Canada....Canada
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<p> </p><p data-start="0" data-end="147"><strong>This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Senior Clinical Research Associate in Canada.</strong></p> <p data-start="149" data-end="1108">This is an excellent opportunity for an experienced clinical research professional passionate about advancing oncology innovation and improving patient outcomes through cutting-edge clinical trials. In this role, you will oversee site monitoring and management activities across early-phase oncology studies, ensuring regulatory compliance, patient safety, and data integrity throughout the trial lifecycle. You will collaborate closely with investigative sites, clinical teams, and stakeholders in a highly dynamic and quality-focused environment. The position offers a balance of remote flexibility and field engagement, allowing you to build strong relationships with leading research centers while contributing to impactful clinical development programs. This role is ideal for a proactive and detail-oriented professional who thrives in fast-paced settings and enjoys mentoring, problem-solving, and driving operational excellence in clinical research.</p> <p></p>\n<p></p><p><br></p><b>Accountabilities:</b><div> <ul data-start="1132" data-end="2384"> <li data-section-id="1e7og3l" data-start="1132" data-end="1304">Manage and monitor oncology clinical trial sites throughout all study phases, ensuring compliance with protocols, regulatory standards, and Good Clinical Practices (GCP).</li> <li data-section-id="157plha" data-start="1305" data-end="1430">Conduct remote and on-site monitoring visits including qualification, initiation, interim monitoring, and close-out visits.</li> <li data-section-id="1pypw54" data-start="1431" data-end="1580">Serve as the primary liaison between clinical trial teams and investigative sites, facilitating clear communication and efficient issue resolution.</li> <li data-section-id="1lbuled" data-start="1581" data-end="1710">Ensure inspection readiness by maintaining accurate documentation, essential files, and Trial Master File (TMF) reconciliation.</li> <li data-section-id="11d9kxy" data-start="1711" data-end="1842">Review site performance metrics, identify operational risks, and implement corrective and preventive action plans when necessary.</li> <li data-section-id="wj9twz" data-start="1843" data-end="1958">Support Institutional Review Board (IRB) and Ethics Committee (EC) submissions and verify approval documentation.</li> <li data-section-id="1trfge" data-start="1959" data-end="2071">Deliver training and ongoing guidance to site personnel on study protocols, SOPs, and regulatory requirements.</li> <li data-section-id="efqcfs" data-start="2072" data-end="2209">Contribute to site feasibility assessments, activation activities, and long-term engagement strategies with oncology research networks.</li> <li data-section-id="1dpa6lj" data-start="2210" data-end="2310">Mentor junior CRAs and support monitoring oversight activities to maintain high-quality standards.</li> <li data-section-id="athlq2" data-start="2311" data-end="2384">Assist sites and stakeholders during regulatory inspections and audits.</li> </ul> <h3 data-section-id="1j0fx74" data-start="2386" data-end="2403">Requirements:</h3> <ul data-start="2404" data-end="3523"> <li data-section-id="1bpltqt" data-start="2404" data-end="2468">Bachelor’s degree in a scientific or healthcare-related field.</li> <li data-section-id="i62gri" data-start="2469" data-end="2593">Minimum of 5 years of independent oncology clinical trial monitoring experience, including both remote and on-site visits.</li> <li data-section-id="bo2dsc" data-start="2594" data-end="2672">At least 1 year of experience supporting early development clinical studies.</li> <li data-section-id="itxg0o" data-start="2673" data-end="2793">Strong understanding of oncology clinical research processes, GxP guidelines, and risk-based monitoring methodologies.</li> <li data-section-id="ui8dgu" data-start="2794" data-end="2879">Experience managing site relationships from study startup through close-out phases.</li> <li data-section-id="17c05de" data-start="2880" data-end="2982">Knowledge of site activation procedures, regulatory submissions, and inspection readiness practices.</li> <li data-section-id="ckdjns" data-start="2983" data-end="3083">Ability to independently identify issues, analyze root causes, and implement effective CAPA plans.</li> <li data-section-id="1g8u7vn" data-start="3084" data-end="3146">Experience training and supporting investigative site staff.</li> <li data-section-id="zck9k9" data-start="3147" data-end="3242">Familiarity with Veeva systems and functional service provider models is considered an asset.</li> <li data-section-id="1yjfvha" data-start="3243" data-end="3320">Excellent organizational, communication, and stakeholder management skills.</li> <li data-section-id="1qqdvla" data-start="3321" data-end="3387">Bilingual proficiency in French and English is highly preferred.</li> <li data-section-id="4fozv3" data-start="3388" data-end="3463">Based in Toronto or Montreal and willing to travel up to 50% as required.</li> <li data-section-id="qcj2y6" data-start="3464" data-end="3523">Must be authorized to work in Canada without sponsorship.</li> </ul> <h3 data-section-id="1iaul7c" data-start="3525" data-end="3538">Benefits:</h3> <ul data-start="3539" data-end="4262"> <li data-section-id="1mmaaz3" data-start="3539" data-end="3568">Competitive salary package.</li> <li data-section-id="kwez41" data-start="3569" data-end="3624">Fully remote work environment with field flexibility.</li> <li data-section-id="1s5wsz1" data-start="3625" data-end="3693">Comprehensive health insurance options for employees and families.</li> <li data-section-id="s0noi7" data-start="3694" data-end="3757">Retirement savings and long-term financial planning programs.</li> <li data-section-id="7nr8ql" data-start="3758" data-end="3809">Generous paid time off and annual leave policies.</li> <li data-section-id="ty20z0" data-start="3810" data-end="3875">Life insurance coverage and employee wellness support programs.</li> <li data-section-id="czbllq" data-start="3876" data-end="3956">Access to a global Employee Assistance Program with 24/7 well-being resources.</li> <li data-section-id="1ck8jm2" data-start="3957" data-end="4086">Flexible country-specific benefits including fitness discounts, travel support, childcare assistance, and wellness initiatives.</li> <li data-section-id="1v9k4c" data-start="4087" data-end="4182">Inclusive and collaborative workplace culture focused on professional growth and development.</li> <li data-section-id="ea0he6" data-start="4183" data-end="4262">Opportunity to contribute to meaningful oncology research with global impact.</li> </ul> </div><p><br></p><p></p>\n<p><strong>How Jobgether works:</strong></p> <p>We use an <strong>AI-powered matching process</strong> to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.</p> <p>We appreciate your interest and wish you the best!</p> <p><a href="https://jobgether.com/how-jobgether-works">&nbsp;Why Apply Through Jobgether?</a>&nbsp;</p> <p>&nbsp;</p> <p><strong>Data Privacy Notice:</strong> By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.</p> <p>&nbsp;</p> <p>&nbsp;</p> <p>#LI-CL1</p>

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