Clinical Research Associate-Freelance

<span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="line-height:normal;">Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today. </span></span></span><br><br><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">TRIO is seeking a <strong>Clinical Research Associate (CRA)</strong> to join our <strong>Monitoring Resource team</strong>. This is a <strong>remote, part-time freelance opportunity</strong> on a <strong>6-month contract</strong>, open to candidates based in Canada.</span></span><br><br><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="line-height:normal;"><span style="vertical-align:baseline;"><b><u><span style="color:#000000;">Responsibilities:</span></u></b></span></span></span></span></span><ul><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">Performing data verification of source documents;</span></span></span></span></span></li><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">Conducting site visits, including pre-study, initiation, monitoring, and termination;</span></span></span></span></span></li><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">Confirming adherence to all FDA, ICH-GCP, and local regulations;</span></span></span></span></span></li><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">Ensuring implementation and compliance with FDA, and ICH-GCP guidelines</span></span></span></span></span></li><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">Participating in budget negotiation and follow-up where applicable</span></span></span></span></span></li><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">Assisting with data validation and query resolution</span></span></span></span></span></li><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">Mentoring junior team members as required</span></span></span></span></span></li><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">Ensuring the completion and collection of regulatory documents</span></span></span></span></span></li></ul><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="line-height:normal;"><span style="vertical-align:baseline;"><b><u><span style="color:#000000;">Qualifications:</span></u></b></span></span></span></span></span><ul><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">A minimum of 2 years of monitoring experience in oncology trials</span></span></span></span></span></li><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">Fluent in French and English</span></span></span></span></span></li><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">Experience monitoring in early-phase trials will be valued. </span></span></span></span></span></li><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">Completion of a science-related Bachelor’s degree</span></span></span></span></span></li><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">Excellent knowledge of medical terminology and clinical monitoring process</span></span></span></span></span></li><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">Strong ICH-GCPs knowledge</span></span></span></span></span></li><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">Experience with clinical trial information systems</span></span></span></span></span></li><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">Ability to travel up to 60% on average</span></span></span></span></span></li><li style="margin-bottom:11px;"><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="background:#FFFFFF;"><span style="color:#000000;"><span style="line-height:normal;">Must be legally authorized to work in the country</span></span></span></span></span></li></ul><div style="margin-bottom:11px;"><br><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.</span></span></div><p><span style="\"font-size:14px\""><span style="\"font-family:Arial,Helvetica,sans-serif\"">Prior to applying please review TRIO's <a href="\"https://drive.google.com/file/d/1OmkMw3kKL1z_Hic3hUqE_P34jSxWdEhT/view?usp=sharing\"">Applicant Information Notice</a></span></span></p> <p><span style="\"font-size:14px\""><span style="\"font-family:Arial,Helvetica,sans-serif\"">To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI.</span></span><br> <br> <span style="\"font-size:14px\""><span style="\"font-family:Arial,Helvetica,sans-serif\"">To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience.</span></span></p> <p style="\"text-align:center\""><strong><span style="\"font-size:20px\""><span style="\"font-family:Arial,Helvetica,sans-serif\"">Teamwork · Passion · Integrity · Innovation </span></span></strong></p>