Assistant Clinical Research Coordinator/assistant(E) Coordinateur(Trice) de Recherche Clinique

The Assistant Clinical Research Coordinator reports to the Manager, Clinical Support. The ACRC is responsible to provide clinical support to the clinic and to Clinical Research Coordinators before and during and after patient visits.

**More specifically, the Assistant Clinical Research Coordinator must**:

- Understand clinical procedures for the studies in which they collaborate ensuring compliance with the protocols;
- Support Clinical Research Coordinators and investigators for several tasks (may include, but not be limited to):

- Prepare in advance material needed for study visits;
- Provide support during patient’s visits;
- Answer basic questions from patients during visits;
- Blood draws, ECG, Blood Pressure, TEWL, medical photography, etc.
- Skin biopsies
- Print source documents and make sure they are always available for research clinic visit.
- Complete and file research documents (source data, medical file);
- Ensure quality control of research and pharmacy files;
- Respond to queries as required;
- Ensure medication management: reception, entry into logs, consignments and destruction;
- Manage follow-up of laboratory and ECG reports;
- Support the Laboratory Coordinator for the processing and shipping of specimens as required;
- Maintain devices, exam rooms and required material;
- Maintain and updates safety equipment and medications;
- May act in a support role in the organisation of the research clinic;
- Follow standard procedures in place (SOPs) and maintaining training records.

**Requirements**:

**Education**
- College Degree in Nursing.

**Experience**
- Minimum de 3 ans d'expérience en soins infirmiers :1 an d'expérience en recherche clinique est un atout ;
- Expérience de travail avec les patients et en recherche clinique.

**Connaissances et compétences**
- Très bien organisé(e);
- Autonome;
- Bilingue (oral et écrit);
- Connaissance de base des logiciels bureautiques (Excel-Word);
- Bonne connaissance des bonnes pratiques cliniques, ainsi que des réglementations et directives applicables de Santé Canada et de la Food and Drug Administration (FDA).

Our company:
**The work environment**

At Innovaderm, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.

In this position, you will be eligible for the following perks:

- Permanent full-time position.
- Complete benefits (medical, dental, vision, RRSP, vacation, personal days, virtual medical clinic, public transportation rebates, social activities).
- Offices near public transportation (Sherbrooke metro station or Saint-Laurent metro station).
- Ongoing learning and development.

**About Innovaderm**

Innovaderm is a contract research organization (CRO) specialized in dermatology. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Innovaderm continues to grow and expand in North America and Europe.

**_
Innovaderm is committed to providing equitable treatment and equal opportunity to all individuals. As such, Innovaderm will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request._**

**_
Innovaderm only accepts applicants who can legally work in Canada._**

Description - Fr:
L'Assistant(e) Coordinateur(trice) de Recherche Clinique (ACRC) relève du Responsable du Support Clinique. L'ACRC est responsable de fournir un soutien clinique à la clinique, ainsi qu'aux Coordinateurs de Recherche Clinique, avant, pendant et après les visites des patients.

Plus précisément, l'Assistant(e) Coordinateur(trice) de Recherche Clinique doit:

- Comprendre les procédures cliniques des études auxquelles ils participent, en veillant à respecter les protocoles ; Soutenir les Coordinateurs de Recherche Clinique et les investigateurs dans plusieurs tâches (qui peuvent inclure, mais ne se limitent pas à):

- Préparer à l'avance le matériel nécessaire pour les visites d'étude ;
- Fournir un soutien pendant les visites des patients ;
- Répondre aux questions de base des patients pendant les visites ;
- Effectuer des prélèvements sanguins, ECG, prise de tension, TEWL, photographie médicale, etc.
- Réaliser des biopsies cutanées ;
- Imprimer les documents source et s'assurer qu'ils sont toujours disponibles pour les visites à la clinique de recherche;
- Compléter et classer les documents de recherche (données sources, dossier médical) ;
- Assurer le contrôle de qualité des dossiers de recherche et des fichiers de pharmacie ;
- Répondre aux demandes de renseignements selon les besoins ;
- Assurer la gestion des médicaments : réception, enregistrement dans les registres, envois et destruction ;
- Gérer le suivi des rapports de laboratoire et d'ECG ;
- Soutenir le Coordinateur de Laboratoire pour le trai