Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...
Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...
In this role, you will collaborate with cross-functional teams, including clinical research associates (CRAs), data managers, and regulatory personnel, to deliver high-quality clinical data while ...
In this role, you will collaborate with cross-functional teams, including clinical research associates (CRAs), data managers, and regulatory personnel, to deliver high-quality clinical data while ...
Associate Director, Regulatory Affairs & Submissions - Nonclinical Development
Montreal, QC · On-site
Conduct gap analyses of nonclinical data packages, identifying risks and defining mitigation ... Excellent analytical, problem-solving, and project management skills. * Strong communication skills ...
Associate Director, Regulatory Affairs & Submissions - Nonclinical Development
Montreal, QC · On-site
Conduct gap analyses of nonclinical data packages, identifying risks and defining mitigation ... Excellent analytical, problem-solving, and project management skills. * Strong communication skills ...
Conduct gap analyses of nonclinical data packages, identifying risks and defining mitigation ... Excellent analytical, problem-solving, and project management skills. * Strong communication skills ...
Conduct gap analyses of nonclinical data packages, identifying risks and defining mitigation ... Excellent analytical, problem-solving, and project management skills. * Strong communication skills ...
Verifies required clinical data entered in the case report form (CRF) is accurate and complete. * Manages reporting of protocol deviations and appropriate follow-up. * Applies query resolution ...
Verifies required clinical data entered in the case report form (CRF) is accurate and complete. * Manages reporting of protocol deviations and appropriate follow-up. * Applies query resolution ...
Nurse
Montreal, QC · On-site
Manage nursing protocols Collect data from standardized clinical data sheets and assess clinical situations Perform various administrative tasks on the computer Answering questions from parents and ...
Nurse
Montreal, QC · On-site
Manage nursing protocols Collect data from standardized clinical data sheets and assess clinical situations Perform various administrative tasks on the computer Answering questions from parents and ...
Clinical Trial Manager
Montreal, QC · On-site
... data verification (SDV/SDR) is performed per the monitoring plan • Monitor Electronic Data ... CLINICAL TRIAL MANAGER, FIRST NAME LAST NAME Only candidates selected for an interview will be ...
Clinical Trial Manager
Montreal, QC · On-site
... data verification (SDV/SDR) is performed per the monitoring plan • Monitor Electronic Data ... CLINICAL TRIAL MANAGER, FIRST NAME LAST NAME Only candidates selected for an interview will be ...
Medical Science Liaison
Montreal, QC · On-site
Deliver balanced, accurate, and non-promotional scientific exchange on disease state, clinical data ... Highly organized, self-directed, and comfortable managing field-based responsibilities, travel ...
Medical Science Liaison
Montreal, QC · On-site
Deliver balanced, accurate, and non-promotional scientific exchange on disease state, clinical data ... Highly organized, self-directed, and comfortable managing field-based responsibilities, travel ...
CRA II / Sr CRA - Sponsor Dedicated | Oncology | Bilingual in French and English (Home-Based - Mo...
Montreal, QC · On-site
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
CRA II / Sr CRA - Sponsor Dedicated | Oncology | Bilingual in French and English (Home-Based - Mo...
Montreal, QC · On-site
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
CRA I / CRA II - Sponsor Dedicated - Bilingual French and English (Home-based - Montreal, Quebec)
Montreal, QC · On-site
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
CRA I / CRA II - Sponsor Dedicated - Bilingual French and English (Home-based - Montreal, Quebec)
Montreal, QC · On-site
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
Clinical Project Manager
Montreal, QC · On-site
We are looking for a Clinical Project Manager to serve as the Regional Lead and the tactical owner ... You have experience with advanced CTMS, eTMF, and EDC platforms, using these tools to drive data ...
Clinical Project Manager
Montreal, QC · On-site
We are looking for a Clinical Project Manager to serve as the Regional Lead and the tactical owner ... You have experience with advanced CTMS, eTMF, and EDC platforms, using these tools to drive data ...
Enter observed clinical data and administer medication: record data and consult work plans (Health Portal Management), administer medication (Xpill Pro). Providing meal service: reheating meals ...
Enter observed clinical data and administer medication: record data and consult work plans (Health Portal Management), administer medication (Xpill Pro). Providing meal service: reheating meals ...
... data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded
... data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded
Partnering across data management, project management, and medical teams to influence enrollment ... We are a clinical-stage biotechnology company focused on discovering and developing antibody-based ...
Partnering across data management, project management, and medical teams to influence enrollment ... We are a clinical-stage biotechnology company focused on discovering and developing antibody-based ...
Fortrea's FSP team is hiring a Clinical Trial Coordinator- Regulatory - Hybrid in Montreal, Canada ... on Fortrea or client data management systems, as assigned by management. * Assistwith the ...
Fortrea's FSP team is hiring a Clinical Trial Coordinator- Regulatory - Hybrid in Montreal, Canada ... on Fortrea or client data management systems, as assigned by management. * Assistwith the ...
As the primary sponsor liaison and advocate, the Clinical Project Manager will plan, execute ... data, documents, equipment and tools, including protocols, SOPs, informed consent forms, case ...
As the primary sponsor liaison and advocate, the Clinical Project Manager will plan, execute ... data, documents, equipment and tools, including protocols, SOPs, informed consent forms, case ...
As the primary sponsor liaison and advocate, the Clinical Project Manager will plan, execute ... data, documents, equipment and tools, including protocols, SOPs, informed consent forms, case ...
As the primary sponsor liaison and advocate, the Clinical Project Manager will plan, execute ... data, documents, equipment and tools, including protocols, SOPs, informed consent forms, case ...
As the primary sponsor liaison and advocate, the Clinical Project Manager will plan, execute ... data, documents, equipment and tools, including protocols, SOPs, informed consent forms, case ...
As the primary sponsor liaison and advocate, the Clinical Project Manager will plan, execute ... data, documents, equipment and tools, including protocols, SOPs, informed consent forms, case ...
Provides therapy area/indication expertise in support of clinical review of clinical data ... Demonstrated experience managing and training large teams in clinical development. * Demonstrated ...
Provides therapy area/indication expertise in support of clinical review of clinical data ... Demonstrated experience managing and training large teams in clinical development. * Demonstrated ...
Project Manager (US/CA)
Quebec, QC · On-site
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... data on complex issues, is responsible for contingency planning and implementation of rescue ...
Project Manager (US/CA)
Quebec, QC · On-site
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... data on complex issues, is responsible for contingency planning and implementation of rescue ...
Clinical Data Manager information
See Quebec salary details
$20.43 - $25.72
4% of jobs
$25.72 - $31.01
5% of jobs
$31.01 - $36.30
9% of jobs
$40.43 is the 25th percentile. Wages below this are outliers.
$36.30 - $41.59
8% of jobs
$41.59 - $46.88
11% of jobs
The median wage is $51.94 / hr.
$46.88 - $52.16
12% of jobs
$52.16 - $57.45
15% of jobs
$60.54 is the 75th percentile. Wages above this are outliers.
$57.45 - $62.74
15% of jobs
$62.74 - $68.03
10% of jobs
$68.03 - $73.32
5% of jobs
$73.32 - $78.61
3% of jobs
$20
$52
$78
How much do clinical data manager jobs pay per hour?
What does a clinical data manager do?
What does a clinical data manager do?
A clinical data manager handles all the data needs of clinical trials for biotechnology and pharmaceutical companies. As a clinical data manager, your responsibilities include the research and storage of data related to clinical trials and programs. Your job duties are to collect, process, and analyze data. You must routinely evaluate your data collection and analysis processes to ensure that results are accurate and valid. You must also ensure that your work is in compliance with ethical research standards and regulations from organizations like the Food and Drug Administration (FDA).
What are the key skills and qualifications needed to thrive as a clinical data manager?
What are some common challenges clinical data managers face when working on multi-site clinical trials?
How much do clinical data managers make in the US?
- How to become a clinical data manager?
- What is the career path for a clinical data manager?
- What is the salary of a clinical data manager?
- What is the difference between a clinical data scientist and a clinical data manager?
- What Is a Clinical Data Manager and How to Become One
- Clinical Data Manager Job Description Sample Template
What are the most commonly searched types of Clinical Data jobs in Quebec?
The most popular types of Clinical Data jobs in Quebec are:
What are popular job titles related to Clinical Data Manager jobs in Quebec?
For Clinical Data Manager jobs in Quebec, the most frequently searched job titles are:
What job categories do people searching Clinical Data Manager jobs in Quebec look for?
The top searched job categories for Clinical Data Manager jobs in Quebec are:
What cities in Quebec are hiring for Clinical Data Manager jobs?
Cities in Quebec with the most Clinical Data Manager job openings:

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 28 days ago
IQVIA rating
8.1
Based on 53 frontline employees who took The Breakroom Quiz
62nd of 226 rated it services
Job description
IQVIA embauche ! Nous sommes a la recherche de plusieurs gestionnaires d'equipe de donnees principaux pour nos modeles de prestation FSP (fournisseur de services fonctionnels) et traditionnels (independants du promoteur).
Postulez des maintenant et votre CV sera examine pour des postes de Responsable d'equipe de donnees senior au sein de differentes equipes. Nous pourrons ainsi vous proposer le projet et l'environnement client les plus adaptes a votre experience et a vos interets !
IQVIA recherche des gestionnaires d'equipe de donnees cliniques experimentes pour superviser la gestion des donnees de bout en bout dans le cadre d'essais cliniques internationaux. Vous assurerez la qualite, l'exactitude et la conformite des donnees tout en dirigeant des equipes multidisciplinaires contribuant au developpement de nouvelles therapies. Ce poste est a pourvoir en teletravail, avec tout le materiel necessaire fourni.
Vos taches:
Gerer la gestion des donnees pour des essais cliniques internationaux complexes, de la mise en place de l'etude au verrouillage de la base de donnees.
Etre la personne-ressource principale du client pour tous les livrables lies a la gestion des donnees.
Superviser la reconciliation des donnees SAE, PK et externes, ainsi que le deploiement de la base de donnees.
Gerer les echeanciers, les budgets et l'affectation des ressources afin de repondre aux attentes du client.
Encadrer les gestionnaires de donnees juniors et promouvoir les meilleures pratiques.
Ameliorer les processus et assurer la conformite reglementaire et aux procedures operationnelles normalisees (SOP).
Profil recherche
Les candidats ideaux possederont...
Un baccalaureat en sciences de la vie, sante, clinique, biologie ou mathematiques.
Au moins 7 ans d'experience directe en gestion de donnees cliniques.
5 ans d'experience minimum a un poste de responsable de la gestion des donnees cliniques (obligatoire).
Vos postes precedents peuvent inclure: gestionnaire de donnees cliniques, gestionnaire de donnees cliniques principal, responsable de la gestion des donnees, gestionnaire de donnees principal et/ou chef de projet en gestion des donnees.
Experience reussie dans la gestion d'etudes internationales de grande envergure (plus de 1000 patients).
Maitrise de Medidata Rave, Oracle InForm ou de systemes EDC similaires.
Solide comprehension des BPC, des directives ICH et des processus de recherche clinique.
Excellentes competences en communication et en leadership.
Une combinaison equivalente de formation et d'experience sera prise en compte.
Une combinaison equivalente de formation et d'experience sera egalement consideree.
Ce qu'IQVIA vous offre
Poste 100 % teletravail - materiel fourni par l'entreprise
Salaire concurrentiel et primes de rendement
Couverture medicale, dentaire et optique des votre premier jour
Regime d'epargne-retraite avec cotisation de l'employeur, assurance-vie et
conges payes a la discretion de l'employeur
Possibilites d'avancement de carriere et de formation grace au mentorat et a la mobilite interne
Culture d'entreprise inclusive et internationale axee sur l'innovation et la collaboration
Apply now and have your resume considered for Senior Data Team Lead opportunities across multiple teams - allowing us to match you with the best-fit project and client environment for your experience and interests!
IQVIA is seeking experienced Clinical Data Team Leads to oversee end-to-end data management delivery for global clinical trials. You'll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life. This is a remote/WFH position with all necessary equipment provided.
What You'll Do
Lead data management for complex, global clinical trials from study setup to database lock.
Serve as the main client contact for all data management deliverables.
Oversee SAE, PK, and external data reconciliation and database deployment.
Manage timelines, budgets, and resource allocation to meet customer expectations.
Mentor junior data management staff and promote best practices.
Drive process improvements and ensure regulatory and SOP compliance.
Who We're Looking For
Ideal candidates will have....
Bachelor's degree in life sciences, health, clinical, biological, or mathematical field.
No less than 7 years of direct clinical data management experience
5+ years in a Lead Clinical Data Management role REQUIRED.
Your previous roles/job titles may include Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager.
Proven success managing large global studies (1000+ patients).
Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.
Strong understanding of GCP, ICH, and clinical research processes.
Excellent communication and leadership skills.
An equivalent combination of education, training, and experience may be considered.
Equivalent combination of education and experience.
What IQVIA Offers
Fully remote role - company equipment provided
Competitive salary and performance-based incentives
Medical, dental, and vision coverage beginning your first day of employment
401(k) with company match, life insurance, and discretionary PTO
Career growth and learning opportunities through mentoring and internal mobility
Inclusive, global culture focused on innovation and collaboration
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 $108,300.00 - $144,452.88. 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 $108,300.00 - $144,452.88. 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.About IQVIA
Sourced by ZipRecruiter
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.
Industry
Health care and social assistance
Company size
10,000+ Employees
Headquarters location
Durham, NC, US