ECG Data Analyst - Safety Pharmacology 1

ECG Data Analyst - Safety Pharmacology 1

ECG Data Analyst - Safety Pharmacology 1

Job Overview

Location
Montreal, Quebec
Job Type
Full Time Job
Job ID
58381
Date Posted
2 years ago
Recruiter
Raymond Catherine
Job Views
356

Job Description

IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.

We are seeking a ECG data analyst for our Safety Pharmacology department site located in Senneville (Montreal).

The following are responsibilities related to the ECG data analyst position:

Evaluation of ECG interval durations, and identification of ECG waveform abnormalities and arrhythmias.

Involved in the analysis of respiratory waveforms.

May contribute to preparation or review of study plans, preparation of reports and SOPs

Assist in the preparation of data for interim reports/updates to the sponsor.

Participation in validation, training, and research & development activities within the department

May interact with sponsors, when requested. May be called upon to exchange with sponsor

Assist in compilation of the historical control data and various other publications.

We are seeking a candidate who:

Possesses a DEC or BSc. or equivalent in science, veterinary medicine, nursing, or related discipline.

Prior experience in ECG evaluations.

Familiarity with GLP regulation guidelines and SOPs, as they apply to regulated research beneficial

Has good interpersonal skills and is able to communicate in English

Has strong organizational skills and attention to detail

Adherence to deadlines and good time management ability

Ideally has a working knowledge of DSI or EMKA physiological platforms.

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

About Safety Assessment

Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

Job ID: 58381

Similar Jobs

Brunswick

Full Time Job

Ecg data analyst - safety pharmacology 1 Ecg data analyst - safety pharmacology 1

Position Overview:The main role of this position will be to focus on assessing a...

Full Time Job

Cargill

Full Time Job

Ecg data analyst - safety pharmacology 1 Ecg data analyst - safety pharmacology 1

Want to build a stronger, more sustainable future and cultivate your career? Joi...

Full Time Job

Labcorp

Full Time Job

Ecg data analyst - safety pharmacology 1 Ecg data analyst - safety pharmacology 1

Job Duties/Responsibilities:Screen and evaluate any gynecologic and non-gynecolo...

Full Time Job

Cigna

Full Time Job

Ecg data analyst - safety pharmacology 1 Ecg data analyst - safety pharmacology 1

ROLE SUMMARYReporting to the Pharmacy Compliance Director, this position will be...

Full Time Job

Cookies

This website uses cookies to ensure you get the best experience on our website.

Accept