10 meilleures offres (clinical trial, ottawa, on) (à pourvoir)

Junior/Intermediate Clinical Trial Associate
The Memory Clinic —Ottawa, ON
- De 60 000 $ à 70 000 $ par an
- Temps plein
- Travail hybride
- Bilingue
- Anglais
- Compétences en communication
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Research Assistant 1 Bruyère Health RI_ Dr. Downar
Bruyère Health Research Institute —Ottawa, ON
- De 25,98 $ à 29,62 $ de l’heure
- Temps partiel
- Travail hybride
- Anglais
- Recherche
- Esprit d'analyse
- Programmes de Bien-être
- Programme d'Aide aux Employés
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il y a 2 jours
Bilingual Sr. Clinical Research Associate
Alimentiv —Ottawa, ON
- De 78 000 $ à 130 000 $ par an
- Temps plein
- Télétravail
- Bilingue
- Anglais
- Déplacements à prévoir
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Bilingual Research Administrative Assistant /Assistant Administrative de Recherche Bilingue
The Memory Clinic —Ottawa, ON
- De 55 000 $ à 65 000 $ par an
- Temps plein
- Bilingue
- Cabinet médical
- Anglais
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il y a 9 jours
Clinical Research Data & Project Coordinator
University of Ottawa Heart Institute —Ottawa, ON
- De 60 000 $ à 82 000 $ par an
- Temps plein
- Microsoft Powerpoint
- Bilingue
- Microsoft Excel
il y a 11 jours
Gestionnaire d'essais cliniques II, IQVIA Biotech/Clinical Trial Manager II, IQVIA Biotech
IQVIA —Ottawa, ON
- De 116 300 $ à 193 800 $ par an
- Temps partiel
- Gestion de projet
- Baccalauréat
Senior Clinical Project Manager, CNS - IQVIA Biotech
IQVIA —Kanata, ON
- De 111 800 $ à 161 800 $ par an
- Temps partiel
- PMP
- Microsoft Office
- Gestion de projet
Chef d’équipe des données (Data Team Lead)
IQVIA —Ottawa, ON
- De 104 700 $ à 154 700 $ par an
- Temps partiel
- Anglais
- Baccalauréat
- Formation et développement
Executive Director
healthcarecan —Ottawa, ON
- Doctorat
- Recherche
- Leadership
Neuromuscular Clinician Investigator (Vacant)
Department of Medicine —Ottawa, ON
- Temps plein
- Bilingue
- Médecine
- Anglais
- Assurance Invalidité
- Assurance Dentaire

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Clinical Trial IWRS Monitor (Overnight)
Everest Clinical Research —Markham, ON
Execute CTT application test planning, test plan, and test script development and Stage I and II testing activities for CTT applications (newly developed…
De 45 000 $ à 65 000 $ par an
Postuler rapidement
il y a 2 jours
Clinical Trial Assistant I
Everest Clinical Research —Markham, ON
Interact with study Sponsors, investigational sites, vendors, and Everest functional groups to enable timely and high-quality operationalization of clinical…
De 45 000 $ à 65 000 $ par an
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Junior/Intermediate Clinical Trial Associate

The Memory Clinic
Ottawa, ON

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Détails du poste

Temps plein
De 60 000 $ à 70 000 $ par an

Profil recherché

Bilingue
Français
Anglais
Compétences en communication

Description complète du poste

Working under general direction of the Manager and/or Director, the Clinical Trial Associate is assigned on Alzheimer’s clinical research trials regulatory tasks. Clinical Trial Associates are primarily responsible for compliance with current regulations, policies, procedures, coordination regulatory documentation activities, IRB submissions, maintain master files (paper and electronic), liaison with the sponsor for startup and ongoing clinical trial activities.

Key Responsibilities:

Clinical Trial Start-up Activities

Prepare, compile, and submit regulatory packages to Sponsor/CRO and Ethics Committees/IRBs.
Coordinate the collection and review of essential study documents, including clinical protocol, Investigator’s Brochure (IB), informed consent forms (ICFs), and site-level documentation.
Ensure compliance with applicable regulations (e.g., ICH-GCP). Track submission status, support regulatory strategy, and collaborate with internal and external stakeholders.

Ongoing Study Management

Prepare and submit regulatory amendments including clinical protocol, Investigator’s Brochure (IB), informed consent forms (ICFs), and site-level documentation.
Manage ongoing submissions including annual reports, safety reports, updated documents
Ensure compliance with regulatory commitments, maintain Investigator Site File/eInvestigator Site File, respond to authority queries, and support audits and inspections including CAPA follow-up.
Act as point of contact for assigned studies, provide guidance to cross-functional teams, collaborate with clinical and start-up teams, and contribute to process improvements.

Training & Study Oversight

Coordinate assignment and completion of training for internal team members and external vendors
Track and ensure training compliance in alignment with study requirements and regulations
Develop and maintain Delegation of Authority Logs to ensure clear documentation of roles and responsibilities

Requirement:

A minimum of 2 years’ experience in a Regulatory Specialist role supporting a clinical site and/or sponsor organization is
Strong attention to detail, excellent organizational and communication skills
Ability to manage multiple priorities and work effectively in a team
Fluency in both French and English (spoken and written) is required
Technical Skills: Knowledge of ICH-GCP and regional regulatory requirements (EMA, FDA, Health Canada). Experience with submission processes and regulatory systems eISF platforms).

Core Competencies

Regulatory & GCP Compliance– Strong understanding of ICH-GCP guidelines, regulatory requirements, and clinical trial documentation standards.
Organization & Attention to Detail– Ability to manage multiple studies, maintain accurate records, and ensure completeness of regulatory documentation.
Communication & Collaboration– Effective communication skills with investigators, sponsors, monitors, regulatory bodies, and internal study teams.
Problem Solving & Critical Thinking– Ability to identify compliance gaps, resolve study-related issues, and support corrective actions in a timely manner.
Adaptability & Time Management– Ability to prioritize competing tasks, meet deadlines, and adapt to changing study and regulatory requirements in a fast-paced environment.

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clinical trial emplois - ottawa, on

Junior/Intermediate Clinical Trial Associate

Research Assistant 1 Bruyère Health RI_ Dr. Downar

Bilingual Sr. Clinical Research Associate

Bilingual Research Administrative Assistant /Assistant Administrative de Recherche Bilingue

Clinical Research Data & Project Coordinator

Gestionnaire d'essais cliniques II, IQVIA Biotech/Clinical Trial Manager II, IQVIA Biotech

Senior Clinical Project Manager, CNS - IQVIA Biotech

Chef d’équipe des données (Data Team Lead)

Executive Director

Neuromuscular Clinician Investigator (Vacant)

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Je souhaite recevoir la dernière alerte emploi pour les postes de ce type : clinical trial (ottawa, on)

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