9 meilleures offres (clinical trial manager, alberta) (à pourvoir)

Research Assistant
Prime Site Research Solutions Inc —Edmonton, AB
- Temps plein
- Google Suite
- Signes vitaux
- Baccalauréat
- Assurance Dentaire
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Clinical Research Coordinator - Genitourinary Group
Alberta Health Services —Edmonton, AB
- De 35,34 $ à 45,03 $ de l’heure
- Temps plein
- Baccalauréat
- Saisie de données
- Systèmes de dossier médical électronique
il y a 4 jours
Research Coordinator
Prime Site Research Solutions Inc —Edmonton, AB
- Temps plein
- Google Suite
- Baccalauréat
- Déplacements à prévoir
- Assurance Dentaire
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Bilingual Clinical Research Associate (CRA)
Medpace, Inc. —Calgary, AB
- Temps plein
- Télétravail
- Anglais
- Microsoft Office
- Bases de données
- Congés payés
- Heures d'arrivée et de départ flexibles
Lead Clinical Research Coordinator
Alberta Health Services —Calgary, AB
- De 31,64 $ à 54,36 $ de l’heure
- Temporaire
- Expérience en supervision
- Gestion de projet
- Capacités de présentation
il y a 4 jours
Research Assistant, Psychiatry
The University of Calgary —Calgary, AB
- Temps plein
- Microsoft Outlook
- Service à la clientèle
- Maîtrise
il y a 4 jours
Clinical Supervisor
Alberta Precision Labs —Edmonton, AB
- De 37,76 $ à 64,76 $ de l’heure
- Temps plein
- Expérience en laboratoire
- Microsoft Office
- Esprit d'analyse
il y a 4 jours
Supervisor
Alberta Precision Labs —Edmonton, AB
- De 37,76 $ à 64,76 $ de l’heure
- Temps plein
- Compétences informatiques
- Recherche
- Expérience en supervision
il y a 6 jours
Chef d’équipe des données (Data Team Lead)
IQVIA —Edmonton, AB
- De 104 700 $ à 154 700 $ par an
- Temps plein
- Télétravail
- Service à la clientèle
- Développement commercial
- Baccalauréat

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Clinical Data Manager
Everest Clinical Research —Markham, ON
A Bachelors’ degree in health and/or pharmaceutical sciences, physical/biological, or chemistry fields with at least 2 years experience in clinical trial data…
De 60 000 $ à 95 000 $ par an
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Clinical Safety Data Associate
Everest Clinical Research —Markham, ON
Develop study safety data review plans and maintain a standard set of data review checklists for clinical trial laboratory data, AEs, serious AEs (SAEs),…
De 60 000 $ à 80 000 $ par an
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Je souhaite recevoir la dernière alerte emploi pour les postes de ce type : clinical trial manager (alberta)

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Research Assistant

Prime Site Research Solutions Inc
Edmonton, AB

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Détails du poste

Temps plein

Avantages

Assurance Dentaire

Compétences

Google Suite
Google Docs
Signes vitaux
Recherche clinique
Tenue des dossiers
Électrocardiogramme
Classement
Gestion des archives
Baccalauréat
Saisie de données
Logiciels de gestion de projet
Gestion des documents
Coordination d'équipe
Permis de conduire

Description complète du poste

Closing date: Hiring multiple candidates - Will remain open until suitable candidate found

Salary: Commensurate with experience

Benefits: Health/dental plan, employee & family assistance program, retirement plan, perks

Start Date: Sep/Oct 2026

Primesite Research Solutions is an Integrative Research Organization and Site Network based out of Western Canada. We conduct phase I, II, III, IV clinical trials in various clinical areas at local hospitals and clinics. We are seeking a research assistant to join our growing site network. This position requires a self-motivated, organized, and accountable individual with strong attention to detail. The applicant must have the ability to prioritize and multi-task in a complex rapidly changing environment and must be able to promote teamwork, collaboration, and problem-solving skills. In this position the research assistant will work under the supervision of the research coordinators and research manager to fulfill clinical trials related responsibilities and ensure that each study progresses efficiently. The research assistant will also be responsible for data entry and management of selected patient registries. This position requires frequent contact with physicians, other staff, study participants, biopharma companies and regulatory agencies, and has significant potential for advancement.

Key Responsibilities:

Adhere to multiple research protocols, confidentiality, ICH, GCP & NIH guidelines
Prepare REB submissions and other regulatory documents required for study initiation
Perform data entry for clinical trials and registries
Prepare for and participate in monitoring visits and conference calls
Develop study files in accordance with various protocols
Provide administrative support including filing, directing phone calls, updating tracking logs and maintaining trial regulatory documents
Organize and maintain project/task management system and clinical trials management system (CTMS)
Organize, prioritize and respond appropriately to incoming correspondence
Maintain optimal office systems, processes and equipment
Coordinate with various departments and correspond with study sponsors and regulatory agencies
Communicate study procedures and provide ongoing support to staff
Screen hospital charts for potential study participants and be able to discuss eligibility with research coordinators and physicians
Organize ongoing patient follow up and study visits
Perform study procedures (including collection of vital signs, blood, ECGs etc) as requested
Comfortable handling and transporting blood, marrow and other lab samples
Travel between hospitals for various tasks
Work effectively with study research coordinators and manager to ensure open communication and efficient prioritization of all assigned responsibilities

Required Skills for Success:

Undergraduate degree required, patient interaction and clinical trials experience are preferred (other education with clinical research experience will be considered)
2-3 years of experience in working with clinical trials/research studies
Must be comfortable interacting directly with patients
Working knowledge of Microsoft Office software (Word and Excel) and Google Apps (Docs and Sheets) required
Tech savvy, willingness to learn and adapt to new technologies, and ability to proficiently use required technologies and applications: online software including for meetings, training, timesheets, project/task management, document management and CTMS
Excellent organizational, communication (oral and written), problem solving and interpersonal skills in dealing with co-workers, clinicians and study participants
Demonstrated ability to take initiative and work in a team environment as well as independently with minimal supervision in a fast-paced environment
Ability to be flexible, assist on multiple projects and successfully prioritize multiple responsibilities to meet deadlines
Work in a professional and ethical manner in accordance with internal policies and procedures, and GCP and ICH guidelines
Self-directed, proactive attitude, highly self-motivated and enthusiastic
Accountable with strong attention to detail and honest in the performance of all responsibilities
Willingness to further professional knowledge by reading journals/books, attending educational sessions, completing training programs as necessary
Own transportation and valid driver's license are beneficial as travel to other sites may be necessary

If you are selected for the next step in the interview process, you will be asked to submit a short one-way video application.

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clinical trial manager emplois - alberta

Research Assistant

Clinical Research Coordinator - Genitourinary Group

Research Coordinator

Bilingual Clinical Research Associate (CRA)

Lead Clinical Research Coordinator

Research Assistant, Psychiatry

Clinical Supervisor

Supervisor

Chef d’équipe des données (Data Team Lead)

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Je souhaite recevoir la dernière alerte emploi pour les postes de ce type : clinical trial manager (alberta)

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