12 meilleures offres (clinical data manager, hamilton, on) (à pourvoir)

SJR - Research Coordinator 1
St. Joseph's Healthcare Hamilton —Hamilton, ON
- De 34,28 $ à 45,70 $ de l’heure
- Temporaire
- Recherche
- Baccalauréat
- Recrutement
il y a 1 jour
Country Study Operations Manager
ICON Plc —Burlington, ON
- Temps plein
- Maîtrise
- Esprit d'analyse
- Gestion de projet
- Assurance Invalidité
- Assurance Dentaire
Clinical Lead/Clinical Team Manager (CTM) - FSP
Thermo Fisher Scientific —Mississauga, ON
- De 145 000 $ à 164 000 $ par an
- Temps plein
- Microsoft Excel
- Microsoft Outlook
- Anglais
il y a 5 jours
Quality Assurance Manager
Intrinsik Corp. —Mississauga, ON
- À partir de 70 000 $ par an
- Temps plein
- Travail hybride
- Expérience en gestion
- Doctorat
- Compétences rédactionnelles
- Assurance Dentaire
- Congés payés
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Chef d’équipe des données (Data Team Lead)
IQVIA —Mississauga, ON
- De 104 700 $ à 154 700 $ par an
- Temps partiel
- Anglais
- Baccalauréat
- Formation et développement
Program Coordinator (Life Science)
Innovation Factory —Hamilton, ON
- De 50 000 $ à 60 000 $ par an
- Temps plein
- Travail hybride
- Bilingue
- Logiciels de GRC/CRM
- Microsoft Excel
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Program Manager (Life Science)
Innovation Factory —Hamilton, ON
- De 60 000 $ à 70 000 $ par an
- Temps plein
- Travail hybride
- Bilingue
- Logiciels de GRC/CRM
- Microsoft Excel
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Site Partner II
ICON Plc —Burlington, ON
- Temps plein
- Anglais
- Baccalauréat
- Compétences en informatique
- Assurance Invalidité
- Assurance Dentaire
il y a 6 jours
Coordonnateur·rice principal·e de la mise en place des projets de laboratoire / Senior Laboratory Project Set-Up Coordinator
IQVIA —Mississauga, ON
- De 60 000 $ à 100 000 $ par an
- Temps partiel
- Expérience en laboratoire
- Anglais
- Bases de données
Chercheur(se) clinicien(ne), Cronos -- Clinical Scientist, Cronos
IQVIA —Mississauga, ON
- De 97 500 $ à 147 500 $ par an
- Temps partiel
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Machine Learning Engineer - Express Scripts Canada
The Cigna Group —Mississauga, ON
- De 115 000 $ à 125 000 $ par an
- Temps plein
- Oracle
- Informatique
- Ingénierie
- Assurance Dentaire
Analyste du cycle de vie des contrats / Lifecycle Contract Analyst
Siemens Healthineers —Oakville, ON
- De 62 500 $ à 89 000 $ par an
- Temps plein
- Bilingue
- Microsoft Excel
- Anglais
- Jours fériés payés
- Congés payés

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

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SJR - Research Coordinator 1

St. Joseph's Healthcare Hamilton
Hamilton, ON

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Détails du poste

Temporaire | Temps plein | Contrat à durée déterminée
Il y a 1 jour

Compétences

Recherche
Baccalauréat
Recrutement
Sens de l'organisation
Compétences en informatique
Compétences en communication
Gestion du temps

Description complète du poste

Position Details

Job Number:

JR00813

Department:

Study Frey OBI 1123

Job Type:

Temporary (Fixed Term), Full time

Work Environment:

In-Person

Contract Duration: (If applicable)

11 months

Number of Positions:

Hourly Rate (Min / Max):

$34.277 - $45.7027

Schedule

Work Days:

Monday to Friday

Time of Day:

Days

Shift:

Hours - 7.5

Shift Start: (If applicable)

Application Dates

Opening Date:

2026-06-23

Closing Date:

2027-06-30

Job Description

Research Coordinator Job Description (Full-time, temporary)

PURPOSE

The Canadian Biomarker Integration Network for Depression (CAN-BIND) is a national research network led by Dr. Benicio Frey with a goal of identifying biomarkers of treatment response in major depressive disorder. We are currently seeking a full-time Research Coordinator at the St. Joseph’s Healthcare Hamilton site to assist with recruitment and assessment of participants for a clinical trial to assess the effectiveness of using biomarkers to allocate participants to treatment with standard antidepressant medications. The ideal candidate will have a University degree in a related field, experience with recruitment of research participants, excellent interpersonal and communication skills, time management skills, organizational skills, problem solving skills, and the ability to manage multiple priorities.

Key Responsibilities and Accountabilities

Collaborates with PI and multidisciplinary research and health care team to recruit and assess study participants (e.g., identifies and screens potential subjects; obtains informed consent; conducts pre-testing and administers questionnaires or other data collection tools)

Plans, implements and coordinates all aspects of data collection and source documentation, in accordance with ICH/Good Clinical Practice guidelines
Identifies problems using assessment skills and reports any abnormalities to the PI and study team, follows up on solutions.
Executes study-related administrative tasks, such as tracking regulatory documents, ethics submissions, payments, invoices and study medication. Keeps organized files of documents, responds to requests for information related to study documentation.
Conducts telephone and/or clinical recruitment interviews to collect data using established criteria
Coordinates patient visits schedule as per study protocol. Responsible for management and collection of clinical questionnaires, EEG data, and biospecimens. Responsible for scheduling study visits with clinicians.
Executes all aspects of study visit (e.g., assessment; adverse events; monitoring of safety; medication; questionnaires; sample collection, processing and shipment of samples) according to clinical protocol. Liaises with clinical labs and pharmacy as needed. Will be trained on collection and upload of EEG data, speech data, biospecimen processing.

· Reviews and assesses study-related literature including SOPs.

· Enters data into secure database as required, liaises with study team and data manager for any concerns.

· Participates in team meetings to report on progress, and identify and resolve potential problems

Minimum Requirements

University Degree in a related field

Certification in Good Clinical Practice; Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans;

Familiarity with Standard Operating Procedures for Clinical Research.

Experience working with clients in a clinical trial setting

Excellent communication and time management skills

Desire to acquire new knowledge and skills

Ability to work as part of a team

Excellent computer skills

St. Joseph’s Healthcare Hamilton (SJHH) is an equal opportunity employer and strives for equity, inclusiveness, and diversity in all our programs, practices, facilities, and people. We foster a culture of patient and staff safety where all positions comply and work in conjunction with the Mission, Vision, and Core Values of SJHH.

We thank all applicants for their interest, however, only those selected for an interview will be contacted. SJHH is committed to a barrier-free recruitment and selection process - please inform us should accommodation be required at any point in the recruitment process.

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clinical data manager emplois - hamilton, on

SJR - Research Coordinator 1

Country Study Operations Manager

Clinical Lead/Clinical Team Manager (CTM) - FSP

Quality Assurance Manager

Chef d’équipe des données (Data Team Lead)

Program Coordinator (Life Science)

Program Manager (Life Science)

Site Partner II

Coordonnateur·rice principal·e de la mise en place des projets de laboratoire / Senior Laboratory Project Set-Up Coordinator

Chercheur(se) clinicien(ne), Cronos -- Clinical Scientist, Cronos

Machine Learning Engineer - Express Scripts Canada

Analyste du cycle de vie des contrats / Lifecycle Contract Analyst

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