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Publié il y a 36 mois

Specialist/Associate, clinical trial

@ FOP Consultants

Québec

Temps pleinTemporaire1+ ans d’expérience
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FOP Consultants is hiring a clinical trial specialist or associate to support (bio)pharmaceutical clients in executing clinical studies. The role covers compliance of operations, materials and regulations, eTMF/TMF record management, and vendor follow-up. The posting states a temporary full-time position, with competitive wages, group and professional insurance, and remote work depending on client needs.

Responsabilités :

  • Support clinical trial teams under protocols and regulations
  • Create and maintain eTMF/TMF records and databases
  • Coordinate quality control of trial documentation
  • Follow up with external suppliers on study progress
  • Prepare minutes and update SOPs

Résumé des exigences :

  • Bachelor's or master's degree in science
  • 1 to 5 years of industry experience, preferably pharmaceutical
  • Clinical research and TMF/eTMF experience
  • Good knowledge of ICH/GCP and Health Canada/FDA rules
  • Fluent communication and writing in French and English

Outils et compétences

Avantages mentionnés

Congés payés
Source et dates

Type de source non vérifié · jsonld

Date publiée par l’employeur
2023-11-16
Première détection par notre source
2026-10-26
Mise à jour du dossier source
2026-11-09

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

Détails du poste

NiveauDébutant
DomaineProfessions paramédicales
Expérience1 an(s) et plus
Heures par semaine40 (estimé)
Milieu de travailBureau, Domicile
PositionSurtout assis
Exigences physiquesphysique faible · ordinateur élevé
LanguesEnglish, French
FormationBaccalauréat (exigé), Maîtrise (préféré)
Domaines d’étudeschemistry, biochemistry, biology, pharmaceutical sciences, pharmacovigilance
Avantages mentionnésCongés payés généreux, Aide au transport en commun

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

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Offres sur Jobsy76
Description

Brief description of the position :

In order to meet the needs of its clients in the (Bio)Pharmaceutical sector, FOP CONSULTANTS is looking for clinical trial specialist/associate consultants motivated to carry out mandates. The main missions would be to ensure the compliance of operations, materials, standards, and regulations during the execution of clinical studies.

Main responsibilities :

Without limitation, the main tasks involve:

  • Support the teams in the execution of clinical trials in accordance with established protocols and procedures and in compliance with regulatory requirements;
  • Create and maintain clinical study databases and records (eTMF, TMF, etc.) to track the execution of the various projects;
  • Coordinate the execution of data quality control (QC) activities to ensure the accuracy of information in eTMF/TMF;
  • Ensures that the necessary equipment and materials are available for the execution of clinical studies;
  • Prepare minutes in accordance with company procedures and regulatory requirements;
  • Collaborate with assigned departments to set up confidentiality agreements (NDA, CDA);
  • Develop or participate in the updating of SOPs;
  • Maintain a good working relationship with all stakeholders (investigators, suppliers, study personnel, etc.);
  • Follow up on the progress of clinical studies with external suppliers;
  • Participate in weekly or monthly meetings on quality assurance files.

Qualifications :

  • Bachelor's or Master's degree in science (chemistry, biochemistry, biology, pharmaceutical, pharmacovigilance, etc.), or any other related discipline;
  • 1 (one) to 5 (five) years of industry experience, preferably in the (bio)pharmaceutical sector;
  • Experience in a similar position in clinical research;
  • Experience in TMF/eTMF management;
  • Good knowledge of ICH/GCP standards;
  • Knowledge of regulations (Health Canada, FDA);
  • Proficient in MS Office;
  • Good communication and writing skills in French and English;
  • Mobility (an asset).

Personal skills :

  • Leadership;
  • Rigor et discipline;
  • (Organize), able to manage several projects;
  • Analytical and critical mindset;
  • Perseverance;
  • Humility.

What we offer :

In order to allow the full development of our team members, FOP CONSULTANTS guarantee the support and comfort necessary for the achievement of their mandate. The main advantages offered are as follows:

  • Competitive wages;
  • Group insurance;
  • Professional insurance;
  • Remote work, according to the customer needs;
  • Vacations: 3 weeks;
  • Paid sick leave: 3 days;
  • Monthly transportation fees;
  • Career advancement opportunity;
  • Continuing education.

Emplois semblables

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    Quebec
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    1+ ansCandidates need a bachelor's or master's degree in a science or clinical field and one to five years of pharmaceutical, biotech or CRO experience, including monitoring visits. They must know ICH/GCP standards and Health Canada and FDA rules, be proficient in MS Office, and communicate well in French and English.

    MS Office

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