... e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines ... data query generation and resolution. May support start-up phase. * Ensure copies/originals (as ...
... e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines ... data query generation and resolution. May support start-up phase. * Ensure copies/originals (as ...
Montreal, QC · On-site
... e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines ... data query generation and resolution. May support start-up phase. * Ensure copies/originals (as ...
Montreal, QC · On-site
... e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines ... data query generation and resolution. May support start-up phase. * Ensure copies/originals (as ...
Identify new vendors, tools, and data sources to deliver innovative epidemiology solutions for ... Experience applying epidemiologic methods inpharmacoepidemiology,clinical development, or outcomes ...
Identify new vendors, tools, and data sources to deliver innovative epidemiology solutions for ... Experience applying epidemiologic methods inpharmacoepidemiology,clinical development, or outcomes ...
Identify new vendors, tools, and data sources to deliver innovative epidemiology solutions for ... Experience applying epidemiologic methods in pharmacoepidemiology, clinical development, or ...
Identify new vendors, tools, and data sources to deliver innovative epidemiology solutions for ... Experience applying epidemiologic methods in pharmacoepidemiology, clinical development, or ...
... of clinical-stage recombinant protein candidates. The Director will also guide the technology ... Provide leadership, mentoring and guidance for protocol execution, data analysis, and technical ...
... of clinical-stage recombinant protein candidates. The Director will also guide the technology ... Provide leadership, mentoring and guidance for protocol execution, data analysis, and technical ...
Montreal, QC · On-site
The role: Evidence Project Management (Mgr EPM) will support the Client Associate Director ... Deep understanding of data sources, clinical systems, and vendor management, with the ability to ...
Montreal, QC · On-site
The role: Evidence Project Management (Mgr EPM) will support the Client Associate Director ... Deep understanding of data sources, clinical systems, and vendor management, with the ability to ...
Montreal, QC · On-site
Clinical Research Associate ICON is a global healthcare intelligence and clinical research ... Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data * Excellent ...
Montreal, QC · On-site
Clinical Research Associate ICON is a global healthcare intelligence and clinical research ... Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data * Excellent ...
COAs are questionnaires completed during clinical trials which allow sponsors to collect data about ... Provides assistance and training to Associate Project Managers during projects at the direction of ...
COAs are questionnaires completed during clinical trials which allow sponsors to collect data about ... Provides assistance and training to Associate Project Managers during projects at the direction of ...
COAs are questionnaires completed during clinical trials which allow sponsors to collect data about ... Provides assistance and training to Associate Project Managers during projects at the direction of ...
COAs are questionnaires completed during clinical trials which allow sponsors to collect data about ... Provides assistance and training to Associate Project Managers during projects at the direction of ...
Montreal, QC · On-site
Perform in-depth data analysis and interpretation for each experiment * Provide clear presentations ... Train Research Associates on sample preparation and analytical techniques * Provide scientific ...
Quick apply
Montreal, QC · On-site
Perform in-depth data analysis and interpretation for each experiment * Provide clear presentations ... Train Research Associates on sample preparation and analytical techniques * Provide scientific ...
$16 - $21.10/hr
PRN associates will be cross-trained in multiple departments as needed. Ready to start a meaningful ... You'll be more than a data collector - you'll be a calm, helpful presence during stressful times.
$16 - $21.10/hr
PRN associates will be cross-trained in multiple departments as needed. Ready to start a meaningful ... You'll be more than a data collector - you'll be a calm, helpful presence during stressful times.
Sherbrooke, QC · On-site
CA$18 - CA$21.75/hr
Refer to the pharmacist all clinical inquiries * Set realistic customer expectations as to wait ... Data entry for new prescriptions, and managing refill request processing * Select medications to ...
Sherbrooke, QC · On-site
CA$18 - CA$21.75/hr
Refer to the pharmacist all clinical inquiries * Set realistic customer expectations as to wait ... Data entry for new prescriptions, and managing refill request processing * Select medications to ...
Quebec, QC · On-site
Administer and adhere to case-management protocols, including clinical monitoring, data collection ... year associate's degree program or equivalent combination of experience and education. Work ...
Quebec, QC · On-site
Administer and adhere to case-management protocols, including clinical monitoring, data collection ... year associate's degree program or equivalent combination of experience and education. Work ...
... clinical studies. In this role, primary responsibilities include: * Write and/or review study ... Review and approve raw data; * Notify the Senior Director, Laboratory Sciences and/or the Associate ...
... clinical studies. In this role, primary responsibilities include: * Write and/or review study ... Review and approve raw data; * Notify the Senior Director, Laboratory Sciences and/or the Associate ...
Administer and adhere to case-management protocols, including clinical monitoring, data collection ... year associate's degree program or equivalent combination of experience and education. Work ...
Administer and adhere to case-management protocols, including clinical monitoring, data collection ... year associate's degree program or equivalent combination of experience and education. Work ...
JOB SUMMARY Under the supervision of the Associate Program Manager, the Reimbursement Specialist ... with data integrity/ rounds as required. Participate in ongoing internal and/ or external ...
JOB SUMMARY Under the supervision of the Associate Program Manager, the Reimbursement Specialist ... with data integrity/ rounds as required. Participate in ongoing internal and/ or external ...
$16.35 - $20.67
9% of jobs
$20.67 - $25
13% of jobs
$26.01 is the 25th percentile. Wages below this are outliers.
$25 - $29.33
16% of jobs
The median wage is $33.65 / hr.
$29.33 - $33.65
13% of jobs
$37.56 is the 75th percentile. Wages above this are outliers.
$33.65 - $37.98
28% of jobs
$37.98 - $42.31
12% of jobs
$42.31 - $46.63
2% of jobs
$46.63 - $50.96
3% of jobs
$50.96 - $55.29
1% of jobs
$55.29 - $59.62
2% of jobs
$59.62 - $63.94
2% of jobs
$16
$35
$63
A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.
| Aspect | Clinical Data Associate | Clinical Research Coordinator |
|---|---|---|
| Primary Role | Manage and ensure accuracy of clinical trial data | Oversee trial operations, patient recruitment, and site management |
| Credentials | Bachelor's in life sciences or related field; familiarity with data management | Bachelor's in health sciences or related field; clinical trial experience |
| Work Environment | Data management teams, clinical trial databases | Clinical sites, hospitals, research facilities |
| Industry Usage | Pharmaceutical companies, CROs, biotech firms | Hospitals, research institutions, clinical trial sites |
While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.
Quebec, QC
Full-time
Posted 22 days ago
8.1
Based on 51 frontline employees who took The Breakroom Quiz
54th of 204 rated it services
Vue d'ensemble du poste
Effectuer des taches de suivi et de gestion de site pour une variete de protocoles, de sites et de domaines therapeutiques. Doit etre bilingue francais et anglais et situe a Montreal.
Responsabilites essentielles
Effectuer des visites de suivi des sites (visites de selection, de lancement, de suivi et de cloture) conformement a la portee contractuelle des travaux et les exigences reglementaires, c'est-a-dire les directives de pratiques exemplaires cliniques (BPC) et de la Conference internationale sur l'harmonisation (ICH).
Travailler avec les sites pour adapter, mener et suivre les plans de recrutement des sujets conformement aux besoins du projet afin d'ameliorer la previsibilite.
Gerer la formation liee au protocole et a l'etude pour les sites assignes et maintenir une communication reguliere avec les sites pour gerer les attentes et les problemes des projets en cours.
Evaluer la qualite et l'integrite des pratiques du site d'etude liees au bon deroulement du protocole et au respect de la reglementation applicable. Soumettre les problemes de qualite a l'echelon superieur, le cas echeant.
Gerer l'avancement des etudes assignees en suivant les soumissions et approbations reglementaires, le recrutement et l'inscription, l'achevement et la soumission du cahier d'observation, ainsi que la generation et la resolution des requetes de donnees. Peut soutenir la phase de lancement.
S'assurer que les copies/originaux (comme requis) des documents du site sont disponibles pour etre classe(e)s dans le dossier permanent de l'essai (DPE) et verifier que le dossier de l'investigateur du site (DIC) est tenu conformement aux directives GCP/ICH et aux exigences reglementaires locales.
Creer et tenir la documentation appropriee concernant la gestion de site, les resultats des visites de suivi et les plans d'action en soumettant des rapports de visite reguliers, et en generant des lettres de suivi et d'autres documents d'etude requis.
Servir de mentor pour le personnel clinique, notamment par des visites de cosuivi et de formation.
Collaborer et assurer la liaison avec les membres de l'equipe de l'etude pour le soutien a l'execution du projet, au besoin.
Le cas echeant, peut etre responsable de soutenir l'elaboration du plan de recrutement des sujets du projet pour chaque site.
Le cas echeant, peut etre responsable de la gestion financiere du site conformement a l'accord d'essai clinique signe et recuperer les factures conformement aux exigences locales.
Diplomes et experience requise
Baccalaureat dans une discipline scientifique ou en soins de sante de privilegie. Requis
Necessite au moins 3ans d'experience en surveillance sur site.
Une combinaison equivalente d'etudes, de formation et d'experience peut etre acceptee a la place d'un diplome.
Connaissance approfondie et aptitude a appliquer les exigences reglementaires applicables en matiere de recherche clinique, c'est-a-dire les lignes directrices des bonnes pratiques cliniques (BPC) et de la Conference internationale sur l'harmonisation (ICH).
Solides connaissances therapeutiques et protocolaires telles que fournies dans la formation en entreprise.
Competences informatiques, y compris la maitrise de Microsoft Word, Excel et PowerPoint et l'utilisation d'un ordinateur portable, d'un iPhone et d'un iPad (le cas echeant).
Competences en communication ecrite et verbale, y compris une bonne maitrise de la langue anglaise.
Solides competences en organisation et resolution de problemes.
Competences de gestion efficace du temps et des ressources financieres.
Capacite a etablir et entretenir des relations de travail efficaces avec les collegues, les responsables et les clients.
Job Overview
Job Profile Summary
Perform monitoring and site management work for a variety of protocols, site and therapeutic areas. Must be bi-lingual in French and English and located in Montreal.
Responsibilities
Essential Functions
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Act as a mentor for clinical staff including conducting co-monitoring and training visits.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
Required Education and Experience
Bachelor's Degree in scientific discipline or health care preferred.
Requires at least 3 years of year of on-site monitoring experience.
Equivalent combination of education, training and experience may be accepted in lieu of degree.
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Strong therapeutic and protocol knowledge as provided in company training.
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
Written and verbal communication skills including good command of English language.
Effective time and financial management skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
IQVIA est un fournisseur mondial de premier plan de services de recherche clinique, d'informations commerciales et de renseignements sur les soins de sante pour les secteurs des sciences de la vie et de la sante. IQVIA se consacre a accelerer le developpement et la commercialisation de traitements medicaux innovants pour aider a ameliorer les resultats des patients et la sante de la population dans le monde entier. Pour en savoir plus, visitez https://jobs.iqvia.com
IQVIA est fiere d'etre un employeur souscrivant au principe de l'egalite d'acces a l'emploi. Tous les candidats qualifies seront pris en consideration pour un emploi sans egard a la race, la couleur, la religion, le sexe, l'orientation sexuelle, l'identite de genre, l'origine nationale, le handicap, l'age, l'etat matrimonial ou tout autre statut protege par la loi applicable. Des mesures d'adaptation pour les candidats handicapes sont disponibles sur demande dans tous les aspects du processus de recrutement. Si vous avez un handicap qui necessite une mesure d'adaptation, nous vous encourageons a contacter notre equipe d'acquisition de talents au workday_recruiting@iqvia.com, afin qu'IQVIA puisse soutenir votre participation au processus de recrutement.
IQVIA s'engage a faire preuve d'integrite dans son processus de recrutement et applique une politique de tolerance zero en matiere de fraude des candidats. Toutes les informations et toutes les qualifications soumises dans votre candidature doivent etre veridiques et completes. Toute fausse declaration, presentation trompeuse ou omission importante au cours du processus de recrutement entrainera la disqualification immediate de votre candidature, ou la cessation d'emploi si elle est decouverte ulterieurement, conformement aux lois applicables. Nous apprecions votre honnetete et votre professionnalisme.
Veuillez noter qu'il est possible que nous utilisions l'intelligence artificielle (IA) dans le traitement de votre candidature. Cependant, nous utilisons l'IA uniquement pour aider notre equipe de recrutement a selectionner ou a evaluer les candidatures, et non pas pour remplacer la prise des decisions par les membres de notre equipe.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law. Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation, we encourage you to contact our Talent Acquisition Team at: workday_recruiting@iqvia.com, so that IQVIA can support your participation in the recruitment process.
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Please note that we may use artificial intelligence (AI) in the processing of your application. However, we only use AI to assist our recruitment team with the screening or assessment of candidacies, and not as a substitute for human decision-making.
La fourchette salariale de base potentielle pour ce poste, annualisee, est de $102,500.00 - $170,900.00. Le salaire de base reel offert peut varier selon plusieurs facteurs, notamment les qualifications liees a l'emploi telles que les connaissances, les competences, la formation et l'experience; l'emplacement; et/ou l'horaire (temps plein ou temps partiel). Selon le poste offert, des regimes d'incitation, des primes et/ou d'autres formes de remuneration peuvent etre proposes, en plus d'une gamme d'avantages sociaux lies a la sante, au bien-etre et/ou d'autres benefices.The potential base pay range for this role, when annualized, is $102,500.00 - $170,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and wellness and/or other benefits.
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At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.
Health care and social assistance
10,000+ Employees
Durham, NC, US
