4 meilleures offres (research coordinator, hamilton, on) (à pourvoir)

CLINICAL RESEARCH COORDINATOR (I)
McMaster University —Hamilton, ON
- De 31,91 $ à 44,92 $ de l’heure
- Temporaire
- Baccalauréat
- Recrutement
- Sens de l'organisation
il y a 7 jours
Clinical Research Coordinator
ClinSurge Research —Stoney Creek, ON
- Temps plein
- Soins infirmiers
- Microsoft Office
- Baccalauréat
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il y a 10 jours
Lab Coordinator
Gay Lea Foods —Hamilton, ON
- De 52 300 $ à 87 100 $ par an
- Temps plein
- Recherche
- Déplacements à prévoir
- Compétences en communication
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Environmental Project Coordinator
exp —Hamilton, ON
- De 65 000 $ à 80 000 $ par an
- Temps plein
- Recherche
- Maîtrise
- Baccalauréat

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CLINICAL RESEARCH COORDINATOR (I)
McMaster University —Hamilton, ON
Education Level Bachelor's degree in a relevant field of study. Bachelor's degree in a relevant field of study. Implement and maintain research project budgets.
De 31,91 $ à 44,92 $ de l’heure
il y a 7 jours

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Clinical Research Coordinator
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Bachelor's degree in health-related field required, Master's degree is an asset. Recognized certification in clinical research (ACRP or SOCRA) is an asset.
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CLINICAL RESEARCH COORDINATOR (I)

McMaster University -
Hamilton, ON

Postuler dès maintenant

Détails du poste

Temporaire
De 31,91 $ à 44,92 $ de l’heure
Il y a 7 jours

Profil recherché

Logiciel statistique
Prévisions financières
Budgétisation et prévisions financières
Recherche clinique
Logiciels de gestion de données
Préparation de demandes de financement
Conception de base de données
Analyse statistique
DME/DSE
Recherche médicale
Baccalauréat
Gestion des données
Préparation de rapports et de présentations
Recrutement
Sens de l'organisation
Compétences en informatique
Gestion de budget
Analyse statistique des données
Compétences en communication
Enseignement
Coordination d'équipe
Rédaction de demandes de subvention
Suivi de l'avancement des projets
Rapprochement de comptes

Description complète du poste

Job ID

78440

Job Title

CLINICAL RESEARCH COORDINATOR (I)

Regular/Temporary

Temporary

Location

HSC- Central Campus

Open Date

2026/08/27

Job Type

Limited Term (>12 months)

Close Date

2026/09/09

Employee Group

Unifor Unit 1, Staff

Favorite Job

Department

Medicine

Full/Part Time

Full-Time

Salary Grade/Band

Grade 8

Salary Range

$31.91 - $44.92 (hourly)

Job Code

JD0570

Existing Vacancy

Yes - Newly Created Position

Contract Duration

12.2 Months

Target Number of Openings

Hours per Week

Posting Details

Schedule

Monday-Friday, 8:30am-4:30pm

Education Level

Bachelor's degree in a relevant field of study.

Career Level

Requires 4 years of relevant experience.

Anticipated Fill Date

October 1, 2026

Existing Vacancy?

Yes, newly created position

Job Description Number

JD00570

Job Description

Job Summary:

We are seeking a highly organized and proactive Clinical Research Coordinator (I) for the Michael G. DeGroote Centre for Transfusion Research (MCTR), in the Department of Medicine. MCTR is dedicated to advancing transfusion science through innovative methodology & collaborative research to improve patient health outcomes.

This position is responsible for implementing, monitoring, refining, analyzing, coordinating, and reporting on several clinical research projects. The successful incumbent will act as a resource for the development of protocols, study documents, operations of study management, and management techniques.

Should the successful applicant be a Unifor Unit 1 bargaining unit member, who meets the eligibility conditions of Article 19.02 of the Unifor Unit 1 Collective Agreement, then the Limited Term Assignment will be defined as a Career Growth Opportunity in accordance with Article 19 of the Unifor Local 5555 Unit 1 Collective Agreement.

Accountabilities:

Apply specialized knowledge and scientific principles to review, critically appraise and interpret published literature.
Write sections of scientific papers, funding proposals, and abstracts.
Coordinate the activities of research staff and resources to ensure that the project progresses in accordance with
predetermined timelines.
Develop estimates of time and resources for research projects.
Oversee the collection, entry, verification, management, analysis, and reporting of data.
Use statistical software to analyze data and interpret results.
Design and maintain databases, data collection forms, error checking methods and related programs for efficient
collection, analysis, and reporting.
Troubleshoot moderately complex computer problems.
Write data management and operations documentation for projects.
Liaise between the clinic centre and remote clinic sites and personnel.
Conduct structured patient interviews.
Ensure that the relevant research methodology is applied and all research material is handled in accordance with
established protocols, policies, and procedures.
Participate in the development of promotional strategies and related materials to encourage participation and support
for research projects.
Consult on protocol development, student organization, and data management activities.
Develop presentations and present information and training sessions to project personnel and project patients.
Present at meetings, seminars, and conferences.
Keep project participants informed of project progress through regular reports and newsletters.
Implement and maintain research project budgets. Create financial projections and make adjustments to research
project budgets throughout the fiscal year.
Exercise appropriate controls, monitor, and reconcile accounts.

Skills and Qualifications:

Bachelor's degree in a relevant field of study.
Requires 4 years of relevant experience.
Experience with the following is also an asset:
- Preference will be given to individuals with experience in data management, including use of REDCap, manipulation of data through Excel, development of database dictionaries, and generating reports for data completeness and compliance.
- Preference will be given to individuals with experience in epidemiology.
- Ability to engage and collaborate with different participating sites.
- Evidence of research training (such as CCRA/C, CCRP, or a similar designation).
- Experience with day-to-day clinical trial operations including patient recruitment and study visits, as well as Health Canada/FDA-regulated trials.
- Knowledge of current Health Canada Division 5, GCP, TCPS 2, and local privacy regulations.
- Experience as a central coordinator for multi-centre trials, including Trial Master File maintenance and oversight of study site activities for the full study lifecycle.
- Experience developing study documents such as protocols, operations manuals, informed consent forms, and lab manuals.
- Familiarity with navigating Epic electronic medical record (EMR) system.
- Experience with submissions to local and provincial Research Ethics Boards (e.g., HIREB, CTO, OCREB).
- Skills in writing grants and funding proposals for both peer-reviewed and industry sources.
- Excellent written and verbal communication skills.
- Highly developed organizational skills and the ability to multi-task under competing priorities and deadlines, including coordinating multiple trials simultaneously.
- Detail-oriented with strong initiative and the ability to work effectively both independently and as part of a team.
- Excellent problem-solving abilities.
- Knowledge of hematology, bleeding disorders, and transfusion medicine is considered an asset.

Additional Information

To apply for this position eligible applicants should submit the following in one PDF document:

Cover letter

Resume

How To Apply

To apply for this job, please submit your application online.

Employment Equity Statement

McMaster University is located on the traditional territories of the Haudenosaunee and Mississauga Nations and within the lands protected by the “Dish With One Spoon” wampum agreement.

The diversity of our workforce is at the core of our innovation and creativity and strengthens our research and teaching excellence. In keeping with its Statement on Building an Inclusive Community with a Shared Purpose, McMaster University strives to embody the values of respect, collaboration and diversity, and has a strong commitment to employment equity.

The University seeks qualified candidates who share our commitment to equity and inclusion, who will contribute to the diversification of ideas and perspectives, and especially welcomes applications from indigenous (First Nations, Métis or Inuit) peoples, members of racialized communities, persons with disabilities, women, and persons who identify as 2SLGBTQ+.

As part of McMaster’s commitment, all applicants are invited to complete a confidential Applicant Diversity Survey through the online application submission process. The Survey questionnaire requests voluntary self-identification in relation to equity-seeking groups that have historically faced and continue to face barriers in employment. Please refer to the Applicant Diversity Survey - Statement of Collection for additional information.

Job applicants requiring accommodation to participate in the hiring process should contact:

Human Resources Service Centre at 905-525-9140 ext. 222-HR (22247), or
Faculty of Health Sciences HR Office at ext. 22207, or
School of Graduate Studies at ext. 23679

to communicate accommodation needs.

Vaccination Mandate - FHS

This position is located in a host hospital or other healthcare site that has an active vaccination mandate in place. Successful applicants will need to comply with these and any other health and safety measures necessary as part of their appointment.

AI Statement

McMaster and its third-party partners may use AI tools to screen, assess, or select applicants during the hiring process. Please note that currently our recruitment platform does not use AI nor is it part of our current recommended recruitment process.

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research coordinator emplois - hamilton, on

CLINICAL RESEARCH COORDINATOR (I)

Clinical Research Coordinator

Lab Coordinator

Environmental Project Coordinator

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