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Publié il y a 8 jours

Clinical Research Associate

@ adecco

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Ottawa, Ontario

80k–85k $/anContratTemporaire2+ ans d’expérience
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Adecco is hiring a full-time contract Clinical Research Associate for a medical device and healthcare technology organization in Ottawa, ON, at $80,000-85,000 per year. The role coordinates clinical studies, maintains trial documentation in Veeva's Trial Master File, conducts monitoring visits and supports site activities, with travel to clinical sites as required. Weekday schedule, Monday to Friday.

Salaire :

80 000 $–85 000 $ par année

Responsabilités :

  • Coordinate and support clinical studies per protocols
  • Manage TMF documentation in Veeva
  • Conduct monitoring visits and site follow-ups
  • Assist with clinical documents, protocols and CRFs
  • Work with internal teams and clinical sites

Résumé des exigences :

  • 2+ years conducting clinical studies
  • Knowledge of clinical research regulations
  • Science degree preferred
  • Experience with medical devices or diagnostics an asset
  • Veeva and TMF experience an asset
  • Legally eligible to work and reside in Canada

Outils et compétences

Veeva

Avantages mentionnés

Assurance maladieSoins dentaires
Source et dates

Site carrière / système de candidatures · careerpage

Date publiée par l’employeur
2026-11-02
Première détection par notre source
2026-10-10
Mise à jour du dossier source
2026-11-02

Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.

Détails du poste

NiveauIntermédiaire
DomaineProfessions paramédicales
Expérience2 an(s) et plus
Heures par semaine40
Horairejour
Déplacementsroute : modérés
Milieu de travailBureau, Chez les clients
PositionAssis et debout
Exigences physiquesphysique faible · ordinateur élevé
LanguesEnglish
FormationBaccalauréat (préféré)
Domaines d’étudesScience
Avantages mentionnésFormation payée

Résumé et détails rédigés par l’IA à partir de l’offre; l’offre de l’employeur fait foi.

Postuler
ChampValeur
Siège socialDüsseldorf
Offres sur Jobsy645
Description

Adecco is currently hiring a full-time Clinical Research Associate for an opportunity with a leading medical device and healthcare technology organization in Ottawa, ON. This role is ideal for candidates with experience in clinical research, clinical studies, medical devices, diagnostics, laboratory operations, regulatory compliance, and clinical trial support.

  • Pay Rate: $80000-85000/year

  • Location: Ottawa, ON

  • Shift: Monday to Friday

  • Job type: Temporary | Full-time

  • Vacancy Status: This posting is for an existing vacancy.

Here's why you should apply:

  • Paid weekly accurate and on time

  • Strong health and safety programs

  • Medical and dental benefits once qualified

  • Free training programs

  • New and quicker onboarding process

Responsibilities:
Clinical Study Coordination

  • Coordinate and support clinical studies in accordance with protocols and regulatory requirements.

  • Collect, maintain, and manage study documentation.

  • Manage Trial Master File (TMF) documentation using Veeva.

  • Conduct monitoring visits, site follow-ups, and visit reporting.

  • Support workflow testing, study preparation, and site activities.

Clinical Documentation & Compliance

  • Assist with the preparation of clinical documents, protocols, CRFs, and reports.

  • Review and document study results.

  • Support the development and maintenance of study procedures.

  • Ensure compliance with quality and regulatory standards.

Collaboration & Site Support

  • Work closely with internal teams and clinical sites.

  • Communicate effectively with study stakeholders.

  • Travel to clinical sites as required to support study activities.

Qualifications and Skills:

  • Bachelor's degree in Science or a related field preferred.

  • Minimum 2 years of experience conducting clinical studies.

  • Knowledge of clinical research regulations and quality standards.

  • Clinical laboratory, medical device, diagnostics, or sample handling experience is an asset.

  • Strong organizational and documentation skills.

  • Excellent communication and interpersonal abilities.

  • Ability to manage multiple priorities in a fast-paced environment.

  • Self-motivated with strong attention to detail and problem-solving skills.

  • Willingness to travel to study sites as required.

  • Experience with Trial Master File (TMF) management and Veeva is considered an asset.

  • Must be legally eligible to work, and reside in Canada

Are you interested in this position? Apply now! Our dynamic team of recruiters will reach out if you qualify for this role.

At Adecco our purpose is simple: to make the future work for everyone. We live our values, Passion, Collaboration, Inclusion, Courage, and Customers at Heart, by fostering a workplace where diversity is celebrated and every voice matters. We encourage applications from individuals of all backgrounds and identities. Together, we’re making the future work for everyone.

Please reach out to learn how the Aspire Academy can upskill you into your next role.



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