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Publisher (Report Services)

  • Montreal, QC, Canada

Salary: $23.00/hr · Full-time

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Job details

Pay
Salary: $23.00/hr
Job type
Full-time
Apply by
Working hours
37.5 hours per week
Posting language
English
Posted

Original job description

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Overview

Publisher - Reporting Services.

As a Publisher for our Reporting Services team at the Senneville location, you will be responsible to format and compile study reports using publishing software and ensuring that reports are prepared as per client requirements and as per industry regulations (FDA, OECD, eCTD, etc.) Ensure quality and scheduled dates are met.

In This Role, Primary Responsibilities Include

  • Format Word study reports as per client format requirements and as per industry regulations.
  • Compile client reports using Publishing software and meeting industry standards.
  • Peer reviews compiled study reports to ensure that quality, client's requirements and industry standards are met.
  • Follow up on compilation issues with the document authors to solve them.

If you have the following qualifications, we'll train you for the rest:

  • Collegial Diploma
  • Previous experience in Publishing or Information Technology
  • Reading and writing English is required. Bilingualism French and English is preferable
  • Proficiency with the Microsoft Office Suite

Role Specific Information

  • Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1
  • Transportation: We offer a shuttle service from Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. In addition, the site is accessible from the Anse-à-l’Orme REM station via STM bus services. Free parking. Electric vehicle charging station.
  • Annual bonus based on performance;
  • Schedule: Monday to Friday, Flexible schedule, depending on the needs, you may have to do overtime.
  • Full-time temporary position (37.5 hours per week) with an anticipated duration of 12 to 18 months. While this is a temporary replacement assignment, this opportunity may eventually lead to a permanent position, subject to organizational needs and the evolution of the role.
  • Salary: $23.00/hr

Why Charles River ?

  • We offer competitive benefits and advantages from day one to support your well-being;
  • Free gym on site;
  • Employee and family assistance program;
  • Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
  • Access to a doctor and various health professionals (telemedicine);
  • 3 weeks’ Vacation & 5 Personal day policy;
  • Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

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 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

About Charles River

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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.

For more information, please visit www.criver.com.

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More about this job

Responsibilities

Format and compile study reports using publishing software, following client requirements and applicable industry regulations and standards. Peer-review reports for quality and compliance, meet scheduled deadlines, and resolve compilation issues with document authors.

Requirements

A college diploma and previous experience in publishing or information technology are requested, and proficiency with the Microsoft Office Suite is required. English reading and writing are required; French-English bilingualism is preferred.

Skills

  • Report Formatting
  • Report Compilation
  • Publishing Software
  • Microsoft Office Suite
  • Quality Assurance
  • Peer Review
  • Regulatory Compliance
  • Document Review
  • English Reading and Writing
  • French-English Bilingualism

Benefits

  • Performance-Based Annual Bonus
  • Free On-Site Gym
  • Employee and Family Assistance Program
  • Career Development Opportunities
  • Telemedicine and Access to Health Professionals
  • Three Weeks of Vacation
  • Five Personal Days
  • Social Activities
  • Free Parking
  • Electric Vehicle Charging Station
  • Shuttle Service

Visa sponsorship

Not detected in the job text

Categories

  • Administrative
  • Healthcare
  • Science & Research

Keywords

  • Study Reports
  • Report Formatting
  • Report Compilation
  • Publishing Software
  • Microsoft Office Suite
  • Client Requirements
  • Quality Assurance
  • Peer Review
  • Document Authors
  • Regulatory Compliance
  • FDA
  • OECD
  • eCTD
  • Industry Standards
  • Good Laboratory Practice
  • Safety Assessment
  • Preclinical Drug Development
  • Toxicology
  • English
  • French

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