Quality Control Associate - CRO

Job Description

<h3>Job Description</h3><p>Job Description<p><p>Pharma Medica Research is a full service contract research organization specialized in conducting early phase clinical trials in healthy volunteers, special and patient populations. We&#39;re currently searching for a <em><strong>Clinical QC Associate</strong></em> <strong>I</strong> to join our growing team!</p><p>The function of the Clinical QC Associate I is to ensure all prepared study source documents and/or forms of clinical activities are in accordance with the protocols, SOPs and regulations at Pharma Medica Research Inc. (<strong><em>PMRI</em></strong>). Review study files upon data entry at the screening, check-in, on-study, and post-study procedures. Observe, on a random basis, the clinical procedures during the conduct of studies and make sure that they are performed in accordance with protocols, <strong><em>PMRI</em></strong> SOPs, GCP requirements and regulations. Review study files after study completion and ensure the documentation is in accordance with protocols, <strong><em>PMRI</em></strong> SOPs, GCP requirement and regulations. This position reports to the Manager, Clinical QC and/or designate.</p><p><strong>Duties and Responsibilities</strong></p><p><strong></strong>1.Prepare study source documents and/or forms in accordance with protocols, PMRI SOPs and regulations.<br><br>2.Review and lock the electronic study setting in accordance with protocols.<br><br>3.Review study tube arrangement for complicated study procedures based on risk assessment. <br><br>4.Review study files upon data entry at the screening, check-in, on-study and post-study procedures.<br><br>5.Observe, on a random basis, the clinical procedures during the conduct of studies (i.e. screening procedures, subject entrance, meals, sample bundling, etc.), and make sure that they are performed in accordance with protocols, PMRI SOPs, GCP requirements and regulations. <br><br>6.Ensure that study files after study completion are accurate and legible according to protocols, PMRI SOPs, GCP requirements and regulations.<br><br>7.Review other study or non-study related documents (e.g. pharmacy and equipment calibration records etc.).<br><br>8.Provide reports on the <span >observations/reviewed</span> data to the relevant <span >supervisors/managers</span> and follow up upon resolution.<br><br>9.Liaise with other departments to improve the accuracy and quality of data.<br><br>10.Perform other assigned duties as required.<br /></p><p><strong><em>Qualifications</em></strong></p><ul><li>College degree or B.SC. in clinical research, health, or science-related field or equivalent.</li><li>At least 1 year of CRO experience or equivalent is an asset</li><li>Good understanding of Phase I study protocols and conduct.</li><li>Good knowledge of GCP requirements.</li><li>Good communication and interpersonal skills.</li><li>Detail-oriented and good organizational skills.</li><li>Excellent computer skills.</li><li>Ability to work both independently and as a team member.</li></ul><p><strong>We Offer</strong><br /></p><ul><li>Competitive compensation plan</li><li>Opportunities for advancement and career progression</li><li>A generous Employee Milestones Awards Program</li><li>Corporate Discounts Program</li><li>Learning Support Programs</li><li>Friendly atmosphere, culture of learning</li></ul><ul></ul><ul></ul><p>Please note all applications must be eligible to work within Canada.</p><p><strong>PMR</strong>I is an Equal Opportunity Employer; promoting accessibility and inclusivity at work and offering accommodation for applicants as required and requested.</p><p>We thank all applicants for their interest; however, only those selected to proceed in the interview process will be contacted.<br /></p><p><strong>If you&#39;re looking for an exciting place to work with an incredible team, apply today!</strong></p><p></p></p></p>