Role Description IQVIA est à la recherche d'un ARC II expérimenté en surveillance d'essais cliniques en oncologie. Ce poste, basé à domicile dans l'est du Canada, nécessite la maîtrise du français et de l'anglais. L'ARC II est responsable de la surveillance des essais cliniques de phase I à IV afin d'assurer la conformité aux protocoles, aux BPC/ICH et aux exigences réglementaires. Elle gère les activités des sites, du début à la clôture. Key Responsibilities - Effectuer les visites de sélection, d'initiation, de suivi et de clôture des sites - Former le personnel des sites aux protocoles d'étude, aux systèmes EDC et aux exigences de l'étude - Assurer la qualité de la documentation source, l'intégrité des données et la résolution rapide des requêtes - Superviser la responsabilité des enquêteurs et la collecte des documents réglementaires - Être l'interlocuteur principal du site et maintenir une communication régulière - Préparer les rapports de suivi conformément aux procédures opérationnelles standard (SOP) et aux échéanciers - Soutenir les réunions des enquêteurs et collaborer avec les coordonnateurs principaux d'étude/ARC Qualifications - Bilingue français-anglais (obligatoire) - Baccalauréat requis. De préférence en sciences de la vie ou dans une discipline connexe - Une combinaison équivalente de formation et d'expérience peut être acceptée au lieu du diplôme - Au moins 1 an d'expérience en suivi sur place (requis) - Disponibilité pour des déplacements à hauteur de 65 à 70 % Benefits - La fourchette salariale de base potentielle pour ce poste, annualisée, est de $84,000.00 - $170,900.00 - Le salaire de base réel offert peut varier selon plusieurs facteurs, notamment les qualifications liées à l’emploi telles que les connaissances, les compétences, la formation et l’expérience; l’emplacement; et/ou l’horaire (temps plein ou temps partiel) - Des régimes d’incitation, des primes et/ou d’autres formes de rémunération peuvent être proposés, en plus d’une gamme d’avantages sociaux liés à la santé, au bien-être et/ou d’autres bénéfices

Role Description Join HIA's growing team of hard working, and dedicated people, who continually grow and improve our company, and services to our clients. Our team of professionals offer abstracting services to our clients with abstracting current cases, backlogs, and reports and many more lines of specialized services. This provides a solution to our clients through outsourcing. HIA is seeking an experienced Blood and Marrow Transplant (BMT) Research Registry Specialist to support the collection, abstraction, management, and submission of transplant data to the Center for International Blood and Marrow Transplant Research (CIBMTR). The ideal candidate will possess strong analytical skills, attention to detail, and experience working with blood and marrow transplant programs and oncology-related registries. This is a remote subcontractor (1099) position requiring a high level of independence, organization, and commitment to data quality and compliance. Must be able to work a minimum of 20 hours per week. Qualifications - Minimum 3–5 years of current Blood and Marrow Transplant Registry experience preferred - Bachelor’s Degree in related area and/or equivalent combination of experience/training - Understanding of medical terminology required - Experience working with CIBMTR reporting and FormsNet preferred - Strong understanding of oncology, hematology, and transplant terminology - Experience abstracting clinical data from electronic medical records - Knowledge of medical terminology, anatomy, physiology, and disease processes - Strong attention to detail and ability to analyze complex medical information - Ability to work independently in a remote environment - Excellent organizational, communication, and time management skills - Proficiency with Microsoft Office, web-based systems, and remote technologies Requirements - Reliable high-speed internet connection - Must have a secure personal computer suitable for remote work - Ability to consistently dedicate scheduled hours weekly - Strong interpersonal and professional communication skills - May require background check and drug screening depending on facility requirements Company Description

Role Description The Medical Policy Research Analyst Intern will primarily identify, appraise, and summarize scientific literature and clinical practice guidelines for the development and implementation of medical policies to be used by Medical Directors, internal clinical staff, and external providers and members. Additionally, the Intern will gain insight into broader projects that may include work on systems for electronic authorizations of medical claims or other ongoing projects. The ideal candidate will have interest in learning about evidence-informed health policy and policy development. - Research, critically appraise, and summarize scientific literature and clinical practice guidelines to develop medical policy and clinical practice guidelines. - Document all research processes and medical policy decisions including literature searches, research summaries, and procedure code (CPT, HCPCS, etc) changes. - Present research and policy recommendations to the Medical Policy Workgroup for approval. - Collaborate and communicate across teams to ensure successful medical policy implementation and maintenance processes are completed. - Participate in Medical Policy team meetings and issue forums. - Additional team duties or projects as assigned or relevant to interests. Qualifications - Must be currently enrolled in a graduate degree program in Public Health, epidemiology, biostatistics, or other closely related field. - Familiarity with anatomy and physiology/disease processes; clinical research methods; medical terminology; and interpretation and application of medical policies. - Knowledge of techniques for conducting literature searches, analyzing and interpreting scientific medical literature for quality of study design and reliability of data. - Familiarity with factors that go into clinical decision-making (evidence, practice guidelines, etc). - Ability to work in a team environment along with the self-motivation to work independently. - Excellent written and verbal communications skills. - Strong organization, time management, problem resolution, and analytical skills. - Strong attention to detail with the ability to identify problems and recommend actionable solutions. - Experience with Microsoft Office applications (e.g. Excel, Word, PowerPoint) and ability to learn new technology quickly and effectively. - Must have a minimum of a 3.0 cumulative grade point average in the current program. Requirements - The expected hiring range for an intern is $22.00 – $27.00 per hour depending on skills, experience, education, and training. Benefits - Work alongside diverse teams building cutting-edge solutions to transform health care. - Earn a competitive salary and enjoy generous benefits while doing work that changes lives. - Grow your career with a company committed to helping you succeed. - Give back to your community by participating in Cambia-supported outreach programs. - Connect with colleagues who share similar interests and backgrounds through our employee resource groups. - Work from home options available for most roles, requiring a wired internet connection with a minimum upload speed of 5Mb and a minimum download speed of 10 Mb. Company Description Working at Cambia means being part of a purpose-driven, award-winning culture built on trust and innovation anchored in our 100+ year history. Our caring and supportive colleagues are some of the best and brightest in the industry, innovating together toward sustainable, person-focused health care. Whether we're helping members, lending a hand to a colleague or volunteering in our communities, our compassion, empathy and team spirit always shine through.

Role Description Premier Research is looking for a Clinical Research Associate I (Canada) to join our Global Clinical Monitoring and Site Management 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. What You'll Be Doing: - Delivers quality, timely monitoring reports for sponsor approval per the Clinical Monitoring Plan (CMP) timelines. - 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, on site or other approved mode of monitoring) with a focus on data integrity and subject safety in accordance with local/regional laws and country specific regulations. - Plans day-to-day activities for monitoring of a clinical study and sets priorities per site. - Prepares for and conducts on site and/or remote qualification, study initiation, interim monitoring, dosing observation, and close out monitoring visits as directed per CMP. - Works with the Clinical Lead or equivalent to enhance and proactively manage site visits and trial issues during the monitoring phase. Qualifications - 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. - Patient facing, study coordinating experience preferred. - Knowledge of ICH-GCP/ISO14155, FDA Guidance Documents, EU Directives, local/regional regulations, and drug/device development and clinical monitoring procedures. - Knowledge of clinical/health systems as well as knowledge of cultural/professional practices appropriate to the country/region where site monitoring activities will be conducted. - Ability to multitask and work effectively with technology and people in a fast-paced environment with changing priorities, self-starter. - Fluency in French is required. Requirements - Travel up to 70-85%. Company Description