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Senior Clinical Research Associate
14 Premier Research Group Canada Limited
Source: Headcount Labs · original listing ↗
Job data: Headcount Labs, ODbL 1.0. Job descriptions belong to their employers.
Posted 3 days ago
About this role
Premier Research is looking for a Senior Clinical Research Associate to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success. * We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. * Your ideas influence the way we work, and your voice matters here. * As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. Join us and build your future here. ROLE RESPONSIBILITIES: * Delivers quality, timely monitoring reports for sponsor approval per the Clinical Monitoring Plan timelines * Maintains submission of expenses according to travel and expense requirements within company guidelines * Responsible for the validity, correctness, and completeness of the clinical data reviewed and collected at assigned sites as dictated by ICH GCP/ISO14155, protocol and client requirements * Monitors (remote, onsite or other approved mode of monitoring) with a focus on data integrity and patient safety in accordance with specific country regulations * Plans day to day activities for monitoring clinical study and sets priorities per site * Prepares for and conducts on-site qualification, study initiation, interim monitoring and close-out monitoring visits at investigator sites as required by clinical monitoring plan. * Takes the initiative to move the project/program forward by reducing backlog and keeping it at a minimum * Monitors with knowledge of quality/scope/timeline and budget parameters * Works with the Clinical Lead or equivalent to enhance and proactively manage site visits and trial issues during the monitoring phase * Monitors the quality of clinical deliverables and addresses quality issues with the appropriate team member. Escalates appropriately and in a timely manner to the appropriate team member. * Manages query resolution process with sites and Premier Research or equivalent Data Management * Maintains Trial Master File (TMF)/electronic Trial Master File (eTMF) as defined by the organization’s processes per filing guidelines. Has an understanding of the required essential documents according to ICH/GCP Appendix C. Reviews site documents and verifies they are accurate, complete, current, and include required updates. * Assists project team with assessing project feasibility and recruitment, as applicable * Maintains project tracking system of subjects and site information, as applicable * Participates in Investigators’ Meeting as designated by the Project Manager * Maintain communication with study sites as directed per CMP, and in agreement with the study site and complete documentation of contacts. * Attends meetings as required * Ensures site visit metrics and utilization are maintained as required and escalates available time as necessary to line manager * Completes timely entry of hours worked and project codes per time entry guidelines * Maintains high level of attention to detail to ensure subject safety for our projects and delivery of quality data for our clients * Acquire basic knowledge of disease or condition under study. Participates in available training offered to increase therapeutic knowledge * Review of IP accountability and applicable logs (subject and site level) as directed per the Clinical Monitoring Plan * Maintains proper, timely communication with study teams and management, as needed. * Completes all required internal training (general and study-specific) on-time. * Identifies confidential information and complies with global and local laws and guidelines * In specific countries or situations, the CRA may be requested to also assume additional country specific responsibilities, being appointed as Subject Matter Expert in one or more areas including but not limited to the following: Start-up, Regulatory, Site Contracts, Office Manager, etc. This will be documented with the appropriate guidance or functional description * In specific projects, the CRA may be requested to also assume additional project specific responsibilities, e.g. Clinical Management for smaller or less complex studies, under the appropriate supervision of the line manager or functional lead * Acts as a resource/mentor for other CRAs and shares knowledge base and best practices * Performs other activities as designated REQUIREMENTS: * Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required * Successful previous experience as a CRA with 4+ years’ experience in clinical trials; previous clinical research experience required, completion of CRA training program * Read, write and speak fluent English; fluent in host country language * Experience in coaching/mentoring other CRAs * Global experience preferred * Experience in monitoring complex trials or global trials or equivalent experience * Knowledge of ICH / GCP regulations * Working knowledge of FDA Guidance Documents / EU Directives / local regulations / ISO14155 regulations, drug / device development, and clinical monitoring procedures * Knowledge of web-based communication tools for conferences and any other IT systems required for the job * Knowledge of clinical/health systems as well as knowledge of cultural/professional practices appropriate to the country/region where the site monitoring activities will be carried out * Full-time availability to internal and external project team members * Excellent team player, collaborative and able to enable an effective team * Ability to multitask and work effectively in a fast-paced environment with changing priorities * Strong verbal and written communication skills * Excellent organizational and time-management skills, able to meet deadlines * Self-starter with a lot of common sense and able to act on own initiative * Accountable, dependable and strong commitment * Applies clear and consistent performance standards and handles problems decisively and objectively * Customer service focused in approach to work, both internally and externally * Maintains a positive, results orientated work environment * Travel: 70-85% * Lifting up to 25lbs * Valid driver’s license, passport as required * Premier Research is more than a company – it’s a community furthering research to improve the lives of patients in critical need. We are a diverse staff thinking creatively, challenging ideas, and solving complex problems. * Our Values – We Aim High, We Work Together, We Stay Agile, We Get It Done, We Care – mirror the determination, flexibility and trust that our team embodies. * As a Premier team member, you have the power to make an impact, regardless of job title and location. * Our dedication to biotech and specialty pharma is unlike any other. * We provide our staff with innovative technologies and continuous learning. Introduce yourself to our Talent Team and we will reach out if there is a role that aligns with your experience and interests. Premier Research is a global clinical research, product development, and consulting company. We are dedicated to helping biotech, specialty pharma, and MedTech innovators transform life-changing ideas and breakthrough science into new medical treatments. Our team is inspired by this common purpose. Premier is a place where you can change lives, and feel rewarded and celebrated. We aim high - we will not stop until we reach our goals. And we care about each other, about our customer and partners, and, most importantly, about all the patients that we touch with our work.