Clinical psychologist Jobs in Quebec City, QC
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Clinical psychologist • quebec city qc
Last updated: 6 hours ago
Be among the first 25 applicants.Direct message the job poster from Teladoc Health.Our Mental Health team at Teladoc Health, comprised of Canadian licensed therapists, psychiatrists, and psychologi...Show moreLast updated: 1 day ago
This is the time to let your talent come to life.To maximize your knowledge and use it for the greater good.To work with the best professionals using state-of-the-art technology, and improve lives ...Show moreLast updated: 30+ days ago
Support customer training and education programs pertinent to Medtronic defined products and technology.Support the implementation of policies and procedures and participate in all facets of clinic...Show moreLast updated: 30+ days ago
Psychologist - Regular full time (100%) Board Office(Complementary Services Department) Nature of the Work The position of psychologist encompasses, in particular, responsibility for prevention and...Show moreLast updated: 30+ days ago
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Works on multiple trials within Oncology.Demonstrated leader...Show moreLast updated: 1 day ago
Our client is an industry leader and manufacturer of medical and aesthetic lasers and light source technologies.At the heart of it, innovation is a fundamental cornerstone of their culture.They str...Show moreLast updated: 30+ days ago
Position Summary As a Clinical Education Specialist at STERIS, you are responsible for professional education of both internal and external STERIS Customers.
You will assist in the development of cl...Show moreLast updated: 6 hours ago
Founded in 1982, WPO is the largest independent provider of holistic wellbeing solutions.Through our customized programs and comprehensive global network of credentialed providers and professionals...Show moreLast updated: 1 day ago
When our values align, there's no limit to what we can achieve.Bilingual- English / French proficiency.The Site Monitor will be responsible for data integrity, data quality and ensuring compliance wi...Show moreLast updated: 30+ days ago
TELUS Health is empowering every person to live their healthiest life.Guided by our vision, we are leveraging the power of our leading edge technology and focusing on the uniqueness of each individ...Show moreLast updated: 30+ days ago
Participates in the preparation and execution of Phase I to IV clinical trials.Oversees the progress of clinical investigations by conducting interim site assessment, initiation, and closure visits...Show moreLast updated: 30+ days ago
Under the supervision of the Executive Director and / or his representatives, the Clinical Assistant will assist the Parole Officer with client workload.
This includes participating in training sessio...Show moreLast updated: 14 days ago
PEN-EA-QUE-182605 Correctional Service Canada - Health Services.Cowansville (Québec), Donnacona (Québec), Drummondville (Québec), Joliette (Québec), La Macaza (Québec), Laval (Québec), Longueuil (Q...Show moreLast updated: 30+ days ago
Management of medium-sized (5-15 countries and / or full service) or large (> .Adherence to and promotion of principles of delivery and service in dealing with PSI customers.Project Supervision of sma...Show moreLast updated: 30+ days ago
QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecula...Show moreLast updated: 30+ days ago
Make a difference in a growing, innovative mental health organization and centre of excellence in people-centered care.Work with supportive colleagues who are passionate about improving lives and c...Show moreLast updated: 30+ days ago
Medical Science Liaison – Neuroscience.The Medical Science Liaison (MSL) will execute the regional field-based strategy for the Medical Affairs team.
As a scientific expert, the MSL will develop and...Show moreLast updated: 3 days ago
- Promoted
Sr Clinical Trial Manager
Syneos HealthQuebec City, QC, Canada Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
We translate unique clinical, medical affairs and commercial insights into...Show moreLast updated: 24 days ago
- Promoted
Virtual Psychiatrist - Mental Health - Quebec Licensed
Teladoc HealthQuebec, Capitale-Nationale, CanadaFull-time
Specialist I, Clinical Solutions - SCI
SysmexQC, CACA$70,200.00 yearly
Assoc Clinical Specialist ENT - Montreal.
MedtronicQuebec, CanadaCA$80,000.00 yearly
Psychologist - Regular full time (100%) - Board Office(Complementary Services Department)
York Region District School BoardQuébec, CanadaCA$75,980.00–CA$94,976.00 yearly
Full-time
- Promoted
Clinical Research Associate - Oncology - Sponsor Dedicated - Montreal or Quebec City
ICON Strategic SolutionsGreater Montreal Metropolitan Area, CanadaFull-time
Spécialiste clinique
RenaudExecQuébecCA$18.00–CA$20.00 hourly
- Promoted
- New!
Clinical Education Specialist
STERISQuébec City, CAFull-time
- Promoted
Director of Child & Adolescent Counselling
Workplace OptionsQuebec, Capitale-Nationale, CanadaTemporary
Site Monitor II- FSP
ParexelRemote, Quebec, CanadaRemote
Full-time
Device Sales Specialist (Montréal) - Bilingual (French)
ICU MedicalQuebec, CA The Device Sales Specialist is responsible for meeting and exceeding an annual sales quota through building and maintaining relationships with key decision makers and stakeholders (Hospital Adminis...Show moreLast updated: 30+ days ago
Psychologist - EAP program (affiliate)
LifeWorksLevis, Quebec, CanadaCA$36.38–CA$45.47 hourly
Part-time
Associé de recherche clinique, – francophone (Canada), IQVIA Clinical Research Associate - French speaking (Canada), IQVIA
IQVIAQuebec City, Quebec, CanadaCA$47,320.00–CA$87,887.80 yearly
Full-time
- Promoted
Assistant Parole Officer
Le Centre de Guérison WaseskunLanaudière-Nord (Saint-Esprit), CanadaFull-time
Psychologist - Inventory
Treasury Board of Canada SecretariatQuébec, QuébecCA$85,917.00–CA$100,165.00 yearly
Senior Clinical Project Manager.
PSIGreater Montreal Area, QUEBEC, CACA$38.79–CA$48.48 hourly
Technical Service Representative - Quebec City, Canada
Ortho Clinical DiagnosticsQuebec, CanadaCA$50,000.00 yearly
Full-time
Mental Health Therapist, First Call Care (Bilingual French)
Homewood HealthQuébec, QC, CACA$77,506.00 yearly
Full-time
Spécialiste en activités cliniques / Clinical activities specialist
CSTUQC, CA Le Centre de santé Tulattavik de L’Ungava est situé à Kuujjuaq.Il dispense l’ensemble des services de santé et services sociaux dans la partie est du Nunavik.
Il dessert sept communautés Inuites ave...Show moreLast updated: 30+ days ago
- Promoted
Medical Science Liaison
MedAccess RecruitersQuebec, Canada, CanadaFull-time
Sr Clinical Trial Manager
Syneos HealthQuebec City, QC, Canada24 days ago
Job descriptionResponsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol / GCP / regulatory compliance and data integrity. Oversees site interactions post activation through site closeout. This may include patient recruitment, investigator payments or other related activities. May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and Categorization Tool (RACT). Reviews the study scope of work, budget and protocol content and ensures the clinical project team (CRAs / CeMs) is aware of the contractual obligations and parameters. Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. Escalates to the project manager any risks to clinical trial management deliverables (timeline, quality and budget) and any activities and requests which are out of contracted scope. Employs strategic thinking and problem-solving skills to propose and implement risk mitigations. Participates and presents in key meetings such as Kick Off Meeting. Serves as an escalation point for communications with investigator site staff and may be required to interact on the phone or in person with principal investigators or other site staff members. This may include accompanying CRA team members to sites for observation or conflict resolution. Collaborates with other functional leaders such as Study Start Up, Patient Recruitment and Data Management to coordinate delivery handoffs and meet expected study milestones such as site activation targets, enrollment targets and database lock timelines. Reviews and provides feedback on other functional plans (e.g. Data Management Plan, Communication Plan) as they relate to the clinical trial management activities. Responsible for development and ongoing maintenance of clinical study tools and templates, including the Clinical Monitoring Plan. Ensures CTMS, dashboards and other systems are set up and available for use by the clinical team, including overseeing user acceptance testing (UAT) as needed. Ensures access and audit trail reviews are conducted as required. Coordinates initial and ongoing training to the study team regarding protocol specificities, Case Report Form (CRF) completion, dashboards, Sponsor Standard Operating Procedures (SOPs), clinical plans and guidelines, data plans and timelines for the study. Oversees resourcing allocations for CRAs and Central Monitors, site assignments and study team members' conduct, and identifies risks to delivery or quality. Ensures quality of the clinical monitoring, central monitoring and site management deliverables within a project and maintain proper visibility of its progress by the use of approved systems and / or tracking tools. Reviews the project oversight dashboards and other clinical trial systems (e.g. Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs), Trial Master File (TMF), IVRS / IWRS, Central Monitoring dashboards), to oversee site and patient activities, study team conduct and to ensure the data has been updated to reflect timely execution of all operational aspects (required visits / calls, duration, and frequency) according to plan. Understands the monitoring strategy required for the study and, where required, participates in the development of the study risk assessment plan. Is accountable for their assigned clinical team members' understanding, ongoing compliance and delivery according to the stated monitoring strategy, CMP / SMP, and risk plans. Reviews the content and quality of site and central monitoring documentation (site monitoring calls, site visit reports, site letters, central monitoring reports and pertinent correspondence), to ensure they represent site management activities and conduct and that they appropriately convey any risks to protocol / GCP compliance, trial conduct, patient safety or data integrity. Document requested revisions and approvals in CTMS. Ensures these deliverables are provided according to company and / or sponsor specifications, including delivery deadlines. Interacts with the client and other functional departments related to clinical monitoring, central monitoring and site management activities and deliverables. Provides status updates on the clinical deliverables and risks to clients, project management and leadership as per departmental or study agreements. Provides solutions for obstacles in protocol execution and site management. Demonstrates understanding of other functions' roles in achieving compliance and delivery according to protocol, SOPs, ICH GCP and country regulations This may include data management, study start up, patient recruitment, medical monitoring, pharmacovigilance and Quality Assurance (QA). Supports Inspection Readiness for clinical trial management scope. Oversees CRAs and Central Monitors assigned to the study and routinely assesses study-specific process and training compliance, CMP compliance, and identifies emerging risks. Develop and support execution of corrective action plans at site and study level. Supports and completes activities to achieve data cut and lock deadlines. Provides feedback to line managers on staff performance including strengths as well as areas for development. May be assigned to larger, more complex trials or may coordinate clinical activities for a team of CTMs across a portfolio of projects May coach and mentor CTMs regarding functional clinical delivery, evaluation of project risks, and action implementation. Bachelor’s degree or RN in a related field or equivalent combination of education, training, and experience Demonstrated ability to lead and align teams in the achievement of project milestones Demonstrated capability of working in an international environment. Demonstrated expertise in site management and monitoring (clinical or central) Preferred experience with risk-based monitoring Demonstrates understanding of clinical trial management financial principles and budget management Knowledge of Good Clinical Practice / ICH Guidelines and other applicable regulatory requirements Must demonstrate good computer skills Strong conflict resolution skills Demonstrated ability to apply problem solving techniques to resolve complex issues and apply a risk management approach to identifying and mitigating potential threats to the successful conduct of a clinical research project. Demonstrates critical thinking to determine the cause and appropriate solution in the identification of issues Moderate travel may be required, approximately 20% Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
Description
Senior Clinical Trial Manager
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know :
WORK HERE MATTERS EVERYWHERE
Why Syneos Health
- We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
- We are committed to our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we’re able to create a place where everyone feels like they belong.
Job responsibilities
Qualifications
What we’re looking for
Get to know Syneos Health
No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health
Additional Information :
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and / or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills / experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.