20 meilleures offres (clinical study manager, mississauga, on) (à pourvoir)

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Unity Health Toronto —Toronto, ON
- De 27,13 $ à 33,91 $ de l’heure
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il y a 4 jours
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Baxter —Mississauga, ON
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Associate Director Study Data Manager
AstraZeneca —Mississauga, ON
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Global Clinical Supply Lead
Amaris Consulting —Mississauga, ON
- De 50 000 $ à 65 000 $ par an
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Bilingual Sr. Clinical Research Associate
Alimentiv —Toronto, ON
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Amaris Consulting —Toronto, ON
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Senior Product Manager, Clinical Workflow Solutions
Clarius Mobile Health —Toronto, ON
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Manager, Clinical Data Management
Alimentiv —Toronto, ON
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il y a 13 jours
Lead Data Manager for Clinical Trials
PSI CRO —Mississauga, ON
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Manager - Clinical Trials - Research Operations Service & Support
CAMH —Toronto, ON
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Clinical Screening Coordinator (Regional West)
Centricity Research —Etobicoke, ON
- De 40 000 $ à 50 000 $ par an
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- Recherche
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Clinical Research Assistant (SRI) - Centre for Clinical Trials - Regular Full-Time 2026-17750
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Microsoft Powerpoint
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Clinical Data Collection Manager
Oncoustics —Toronto, ON
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Territory Manager--Ontario West Manitoba
AngioDynamics —Toronto, ON
- Temps plein
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Territory Manager, Mississauga/Oakville
Straumann —Toronto, ON
- Temps plein
- Microsoft Powerpoint
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Chercheur(se) clinicien(ne), Cronos -- Clinical Scientist, Cronos
IQVIA —Mississauga, ON
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Clinical Team Lead, Phase I
Fortrea —Toronto, ON
- Fins de semaine au besoin
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il y a 6 jours
QA Associate – Biologics - Eurofins CDMO Alphora, Inc.
Eurofins Canada BioPharma —Mississauga, ON
- 70 000 $ par an
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- Assurance Invalidité
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il y a 12 jours
Project Manager/Sr. Project Manager (Oncology experience required)
Ergomed —Mississauga, ON
- Temps plein
- Télétravail
- Esprit d'analyse
- Baccalauréat
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il y a 1 jour

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Research Assistant I Dialysis Research

Unity Health Toronto -
Toronto, ON

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Détails du poste

Temporaire | Temps plein
De 27,13 $ à 33,91 $ de l’heure
Il y a 4 jours

Profil recherché

Utilisation d'un ordinateur
Exploration de données
Expérience en gestion
Traitement de texte
Classement
Bases de données
Baccalauréat
Compétences en informatique
Secrétariat
Gestion du temps

Description complète du poste

Research Assistant

Dialysis Research

Dialysis Research is currently looking for a Research Assistant I for the St. Michael’s and St. Joseph’s Research Teams.

The primary role of the Research Assistant I includes providing essential assistance, organizational and administrative support to research projects at a basic level. Tasks may include collecting and recording data through survey and in-depth interviewing, processing of data, following research procedures, screening of study participants including obtaining consent (if applicable), labeling and shipping samples and study related material. In general, the role provides project support for the Research team and Principal Investigators. Research Assistants also contribute to the funding and grant processes by providing information, helping quality check documentation, and liaising with internal and external partners. Research may take place in a clinical, community, or laboratory setting and thus tasks may vary depending on the nature of the research.

This is an entry level role with potential for progression to level II and potentially Research Coordination. Don’t meet every single requirement? Studies have shown that people in underrepresented communities are less likely to apply to jobs when they don’t meet every single qualification. We are dedicated to building an inclusive workplace, so if you’re excited about this role but your past experience doesn’t align perfectly, we still welcome you to apply.

Duties & Responsibilities: Due to variable nature of position, this list is to be used as a guide only. Administrative Duties (60% of work time)

General office (incld. virtual) duties, e.g., filing, mailings, courier services, photocopying, printing, scanning, distributing information etc. Orders supplies, maintains inventory, and ensures supplies are accessible to research staff.

Organizes office/lab space.

Maintains calendars and manages complex scheduling requests.

Develops correspondence and other relevant documentation, including letters, memos, reports, invoices, abstracts, forms etc. to support the activities of the research team and Principal Investigator.

Reviews slides for webinars, written study reports, scientific meetings, and conferences.

Organizes video/teleconference meetings for research studies, including contacting attendees, and preparing meeting materials.

Participates in database processing and management.

Coordinates communication between team, and external partners.

Prepares REB/CTO submissions relative to the initiation and conduct of individual studies. Registers study protocols.

Collects conflict of interest forms.

Helps maintain CVs of the PIs, and external partners.

Updates monitoring logs i.e., 70 freezer logs, sample storage logs, etc.

Non-Laboratory Research Tasks

Collects, transcribes, organizes, quality controls, and enters study related data.

Collects, compiles, updates, and provides basic statistical information, and other data to generate and prepare reports and other documentation to support study related data.

Interacts with various departments such as pharmacy, laboratories, medical records, etc., and with internal and external stakeholders in order to provide administrative support.

Performs literature searches/data mining on requested topics through databases and provide relevant articles to PI or research team.

Understands, interprets, and processes data.

May assist with manuscript and report writing, and literature reviews.

Collects feedback from multiple partners on projects re: proposals, manuscripts, and dissemination tools (sometimes >50 authors) including record keeping of feedback and changes to authorship order

Recruitment and Coordination of Study Participants

Screens participants and obtains required documentation including obtaining consent.

Collects data via phone calls, interviews.

Recruits study participants, in collaboration with study team or staff at participating community organizations.

Schedules interviews and participants.

Follows strict protocols for participant interactions.

Acts as the on-site point of contact for the studies at participating community/healthcare organizations.

Administers quantitative surveys to study participants at participating community organizations using online survey tool (data collection).

Facilitates compensation of study participants +under direction of study team/PI

Travels to participant sites as required. Laboratory Tasks

Prepares routine media, solutions, and reagents.

Performs well-defined, routine and repetitive tests, experiments or other procedures.

Performs cross functional and other duties as assigned and/or requested. All staff are expected to carry out their assigned duties and responsibilities in a manner which prioritizes patient and employee safety and confidentiality. Key accountabilities in this regard include:

Strict compliance with patient/employee confidentiality practices and policies.

Strict compliance with patient/employee safety practices and standards.

Appropriate identification, reporting, and response to patient/employee confidentiality breaches in accordance with established policies and procedures.

Appropriate identification, reporting, and response to patient/employee safety risks and incidents/events in accordance with established policies and procedures.

Qualifications:

Undergraduate Degree or 1 year of relevant experience OR demonstrable equivalent combination of specialized education and experience.

TCPS CORE 2 is preferred (Completed within first 2 weeks of hire)

Good clinical practice certificate is an asset (Completed within first 2 weeks of hire)

Basic computer skills, particularly database, spreadsheet and word processing.

Experience with a reference manager (i.e. EndNote, Mendeley, etc.) is an asset.

Intermediate Organizational and time management skills, including multi-tasking and flexibility to adapt to changing workload.

[Basic] Problem Solving

[Intermediate] Communication (verbal/written) and interpersonal skills.

[Basic] Computer Skills

[Basic] Ability to work independently and as part of a team.

[Basic] Excellent attention to detail.

[Basic] Proven ability to learn new skills.

[Basic] Progressively responsible experience in a clerical position.

Unity Health Toronto is committed to creating an accessible and inclusive organization. We strive to provide a recruitment process that is barrier-free and in compliance with the Accessibility for Ontarians with Disabilities Act (AODA) and the Ontario Human Rights Code. We understand that you may require an accommodation at any stage of the recruitment process. When you are contacted, please inform the Talent Acquisition Specialist and we will work with you to meet your accommodation needs. We want to emphasize that all accommodation requests are handled with the utmost confidentiality, respecting your privacy and dignity.

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Je souhaite recevoir la dernière alerte emploi pour les postes de ce type : clinical study manager (mississauga, on)

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