Clinical Research Specialist

**Posting Period**
From February 11, 2025
to March 25, 2025

**Country or region**
Canada

**Location**

Montréal, Québec

**Business Unit**
Health Solutions

**Department**
Research and Development

**Entry date**
As soon as possible

**Job Status**
Permanent - Full time

**Minimal required work experience**
0 to 1 year

**Minimal education level required**
Master's Degree

**Work schedule**
37,5/hours per week from Monday to Friday

**Salary**
To be determined

**Benefits**
Competitive social benefits

**Clinical Research Specialist (N-2501)**:
**Main Functions**:
Under the direct supervision of the Clinical Operations Director, the Clinical Research Specialist (CRS) will be responsible for the oversight of evidence-based clinical trials of Lallemand probiotic strains and yeast formulations. The CRS will also be responsible for managing clinical trial documentation and implementing applicable regulatory requirement(s). Additionally, the CRS will be responsible for ensuring that all clinical trials are conducted in accordance with ethical principles and following the principles of International Conference for Harmonization Good Clinical Practice (ICH GCP).

**Responsibilities**:

- Oversee and coordinate clinical trials of the Lallemand Health Solutions clinical portfolio;
- Evaluate and manage project budgets and resources;
- Take part in the writing and/or revise protocols and other study related documents (Case Report Forms (CRFs), Informed Consent Forms (ICFs), Statistical Analysis Plan (SAP), etc.);
- Coordinate the supply of Investigational Products (IP) and other study supplies to the clinical site(s);
- Perform search and evaluation of Clinical Research Organizations (CROs), clinical sites, universities or Principal Investigators for potential trials;
- Prepare and perform continuous monitoring during the study (i.e.; Site Initiation Visits (SIV), Monitoring Visits (MV), Close Out Visits (COV), monthly updates reports) of CROs, clinical sites, or universities to ensure the conduct of the trial is in accordance with approved protocol/amendments and following GCP requirements;
- Write monitoring reports to document site visits and findings;
- Coordinate the analysis of study samples;
- Take part in analysis of the study results;
- Coordinate the redaction of study reports or manuscripts for publication;
- Present findings at scientific congresses or meetings;
- Design, write and update documentation and templates related to the management of clinical operations;
- Assist with other project management duties as assigned by the Clinical Operations Director.

LI-DNP

**Technical skills**:
Required
- M.Sc. or Specialty Diploma in Clinical Research Assistant School or related field;
- Knowledge of guidelines and regulations regarding Good Clinical Practice (GCP) and clinical trial regulations in Canada and USA;
- Ability to write scientific reports and excellent oral and written communication skills in English and French;
An asset
- Previous clinical research experience preferred;
**Personal abilities**:
Required
- Attention to detail and ability to work independently;
Other
- Possess excellent organization, project management and critical thinking skills.

**Organization**:
Lallemand is a privately held Canadian company founded in the late 19th century, which develops, produces, and markets microorganisms for various markets. The administrative offices of the parent company are in Montreal, Canada. Today, Lallemand employs more than 5,000 people working in more than 45 countries on 5 continents.

Lallemand Health Solutions specializes in the production of probiotics intended to serve the agri-food, parapharmaceutical, and pharmaceutical industries. With its manufacturing processes adhering to the highest standards of quality, the company provides probiotic strains that help millions of people improve their health and well-being.

On top of its extensive portfolio of ready-to-use probiotics (Lacidofil®, Probiokid®, Probio'Stick®, Protecflor®), the Health Solutions branch also tailor-makes unique formulas to respond to clients' unique needs. This process employs the Harmonium, Lafti®, or Rosell® strains.

The Lallemand Health Solutions team enjoys a stellar reputation, as one of the only companies that is authorized to produce the S.boulardii strain. Whether in North America, Europe, or Asia, your next pro-fessional challenge awaits you at Lallemand
- Please take note that accommodations will be provided in all parts of the hiring process. Applicants need to make their needs known in advance._