Average salary: $104,406 /yearly
More statsSearch Results: 170 vacancies
...The RI-MUHC is supported in part by the Fonds de recherche du Québec - Santé (FRQS).
Position Summary
CANTRAIN is a national clinical trial training program (CTTP) in response to a call by the Canadian Institutes for Health Research (CIHR). Its vision is to offer the...
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...Position Summary
Under the supervision of the manager of the Clinical Research Unit in cardiac electrophysiology and the Principle Investigator... ...,
Timely completion of electronic CRFs as for clinical trial requirements,
Respond promptly to queries and requests for information...
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...conduct research and research training in health and illness with the goal of facilitating the development and implementation of clinical trials, biobanks, cancer control, and nurse-initiated studies and protocols. Ongoing efforts to strengthen the interdisciplinary aspects...
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...the project manager and the principal investigator. The successful candidate will be responsible for the day-to-day management of clinical trials in pediatric neurosciences.
General Duties
Obtains informed consent, assesses patients for protocol eligibility through...
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..., resources, facilities, equipment and staff to conduct the clinical study throughout the study period. Trains investigational site... ...experience
Extensive on-site monitoring experience in phase 2/3 trials, ideally with experience of complex trials in oncology or rare disease...
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Full time
Remote job
Interim role
...The RI-MUHC is supported in part by the Fonds de recherche du Québec - Santé (FRQS).
Position Summary
CANTRAIN is a national clinical trial training program (CTTP) in response to a call by the Canadian Institutes for Health Research (CIHR). Its vision is to offer the...
Suggested
Holiday work
Full time
Temporary work
Traineeship
Work experience placement
Internship
Local area
Shift work
...title possibly developing into a senior position within 2 years.
General Duties
Recruitment of participants,
Participating in clinical and administrative aspects of study visits including:
Scheduling of study visits as per protocol,
Conducting the informed...
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Description
Position Overview
Responsibilities
Qualifications
Required Knowledge
Required Skills & Abilities
Required Professional Designation/Certification
Required Experience
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Full time
...Clinical Statistician programmer Role
The clinical statistical programmer will be responsible for providing study level statistical expertise... ...support.
You carry experience in statistical or clinical trial methodology research and presentations on statistical methods,...
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Full time
Contract work
Internship
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...Master's Degree
Field of Study: Public health, epidemiology, or other related fields
Work Experience
A minimum of two years of clinical research experience in an academic environment or/and in a clinical research organization required,
Work experience in the field...
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...RI-MUHC is supported in part by the Fonds de recherche du Québec - Santé (FRQS).
Position Summary
Under the supervision of the Clinical Research Coordinator of the Research Injury Repair Recovery Program (IRR) RI-MUHC - Orthopaedic Surgery/ Arthroplasty , the incumbent...
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...Role The Study Lead Clinical Statistician will be responsible for supervising/managing, overseeing and validating all statistical activities... ...studies
You have experience in statistical or clinical trial methodology research and presentations on statistical methods, clinical...
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...direct report to the Chief Technology Officer (CTO), the Director of Clinical Technologies assumes a critical role in the oversight of... ...company’s corporate values.
Advocate for the Physicians’ and Clinic’s best interest in front of ELNA leadership.
Project Management...
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Full time
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Monday to Friday
...biopharmaceutical and medical devices industries with a broad range of clinical research services from early to late-stage clinical development,... ...Bioanalytical studies.
A clear understanding of clinical trials and an ability to perform your duties without assistance....
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...un-blinding (e.g., continuously supporting study statisticians, trial supply managers and other central functions from concept protocol... ...Manage and lead interactions with:
Study statisticians
Clinical Trial Supply Managers and Trial supply assistants
Study Managers...
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...role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
Job Summary
As a Clinical Veterinarian for our team located in Laval , you will be responsible for the well-being of our quarantine laboratory animals. Your...
Permanent employment
Full time
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Internship
Worldwide
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Monday to Friday
...Job Description
The Clinical Supply Chain Specialist supports the Supply Chain Study Lead (SCSL), Supply Chain Managers (SCMs) and Supply... ...relevant documentation is archived and posted in the electronic Trial Master.
File (eTMF) at different milestones and maintain the...
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...of our leading edge technology and focusing on the uniqueness of each individual to create the future of health.
Our TELUS Health clinic is looking for an Administrative Coordinator to join our dynamic and professional team. Through inspired, innovative and effective...
Full time
Flexible hours
Shift work
...(FRQS).
Position Summary
Under the supervision of the Manager of Oncology Research, Centre for Innovative Medicine (CIM), the Clinical Research Coordinator – Nurse is responsible for supporting the successful conduct of clinical research studies in oncology. The incumbent...
Holiday work
Full time
Flexible hours
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...multidisciplinary team of healthcare professionals and our high quality clinical programs allow us to offer our patients the “Elna experience”.... ...in a full range of medical services, all under one roof. Our clinics are ultra-modern and the environment is both peaceful and...
Full time
Remote job
Saturday