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Drug Development Jobs in Quebec (NOW HIRING)

Facility Coordinator

Montreal, QC ยท On-site

  • Medical

  • PTO

... drug development cycle, from discovery to late-stage clinical trials. The Company operates globally with facilities located in Canada, USA, Belgium, Australia, and China. Joining CellCarta means ...

We offer competitive wages and professional development opportunities, along with opportunities to engage with a community of clinicians from a variety of professional backgrounds across Canada who ...

EAP Counsellor

Brossard, QC ยท Hybrid

  • Medical

  • Dental

  • Vision

  • PTO

Clinical supervision and career development opportunities; * Purpose & Culture: A positive work environment that supports diversity, inclusion, and compassion. Advantages for those working 3 days ...

EAP Counsellor

Dorval, QC ยท Hybrid

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Coverage for professional membership, paid training leave, clinical supervision, and career development opportunities; * Retirement Plan: Employer-contributed plan to help you reach your financial ...

EAP Counsellor

Montreal, QC ยท Hybrid

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Coverage for professional membership, paid training leave, clinical supervision, and career development opportunities; * Retirement Plan: Employer-contributed plan to help you reach your financial ...

EAP Counsellor

Longueuil, QC ยท On-site +1

  • Medical

  • Dental

  • Vision

  • PTO

Clinical supervision and career development opportunities; * Purpose & Culture: A positive work environment that supports diversity, inclusion, and compassion. Advantages for those working 3 days ...

EAP Counsellor

Boisbriand, QC ยท On-site +1

  • Medical

  • Dental

  • Vision

  • PTO

Clinical supervision and career development opportunities; * Purpose & Culture: A positive work environment that supports diversity, inclusion, and compassion. Advantages for those working 3 days ...

EAP Counsellor

Sherbrooke, QC ยท Hybrid

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Coverage for professional membership, paid training leave, clinical supervision, and career development opportunities; * Retirement Plan: Employer-contributed plan to help you reach your financial ...

Showing results 41-60

Drug Development information

What is drug development?

Drug development is the process of bringing a new pharmaceutical drug to market. It involves several stages, including drug discovery, preclinical research, clinical trials, and regulatory approval. Each stage is designed to ensure the safety, efficacy, and quality of the drug before it can be made available to patients. The entire process can take several years and requires collaboration between scientists, clinicians, regulatory agencies, and pharmaceutical companies.

What are the typical stages of collaboration between different teams in a drug development role?

In drug development, professionals regularly collaborate across multidisciplinary teams, including research scientists, clinical trial coordinators, regulatory affairs specialists, and manufacturing experts. Early stages involve close work with research and discovery teams to identify promising compounds, followed by coordination with clinical teams during trial phases, and finally with regulatory and production teams as the drug moves toward approval and commercialization. Effective communication and cross-functional teamwork are essential, as each stage relies on timely data sharing and joint problem-solving to navigate complex challenges.

What are the key skills and qualifications needed to thrive in drug development, and why are they important?

To thrive in Drug Development, you need a strong background in pharmaceutical sciences, biology, or chemistry, often supported by an advanced degree (e.g., PhD, PharmD, or MSc). Familiarity with regulatory compliance, clinical trial management systems, and data analysis software such as SAS or R is typically required. Excellent problem-solving, project management, and cross-functional communication skills help professionals excel in this multidisciplinary field. These competencies ensure that new drugs are developed safely, efficiently, and in accordance with regulatory standards.

What is the difference between Drug Development vs Pharmacologist?

AspectDrug DevelopmentPharmacologist
Required CredentialsBachelor's or Master's in Pharmaceutical Sciences, Chemistry, or related fields; often requires experience in clinical trialsDegree in Pharmacology, Pharmacy, or related fields; may require licensing or certification for clinical practice
Work EnvironmentResearch labs, pharmaceutical companies, clinical trial sitesResearch labs, hospitals, academic institutions, regulatory agencies
Industry UsageDeveloping new drugs, overseeing clinical trials, regulatory submissionsStudying drug effects, mechanisms, safety, and efficacy; advising on drug use

While both roles are integral to the pharmaceutical industry, Drug Development focuses on creating and bringing new drugs to market through research, testing, and regulatory processes. Pharmacologists primarily study how drugs interact with biological systems, often working in research or clinical settings to understand drug effects and safety. The two roles often collaborate but differ in their core responsibilities and career focus.

How do you get into drug development?

To enter drug development, individuals typically need a background in life sciences such as biology, chemistry, or pharmacology, often supported by a relevant bachelor's or advanced degree. Gaining experience through internships, research projects, or entry-level roles in pharmaceutical or biotech companies can be valuable, along with developing skills in laboratory techniques, data analysis, and regulatory compliance.

How much do drug development professionals make?

Drug development professionals, including roles such as research scientists and clinical trial managers, typically earn between $70,000 and $130,000 annually, depending on experience, education, and location. Entry-level positions may start lower, while senior roles with advanced skills and certifications can exceed this range.

What career develops drugs?

A career in drug development typically involves roles such as pharmacologist, medicinal chemist, clinical researcher, or regulatory affairs specialist. These professionals work in laboratories, research institutions, or pharmaceutical companies to discover, test, and bring new drugs to market, often requiring knowledge of biology, chemistry, and regulatory processes.

What are popular job titles related to Drug Development jobs in Quebec?

For Drug Development jobs in Quebec, the most frequently searched job titles are:

What job categories do people searching Drug Development jobs in Quebec look for?

The top searched job categories for Drug Development jobs in Quebec are:

What cities in Quebec are hiring for Drug Development jobs?

Cities in Quebec with the most Drug Development job openings:

Infographic showing various Drug Development job openings in Quebec as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 1% Temporary, and 3% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution.

Proposal Specialist - Hybrid (Montreal Area)

CellCarta

Montreal, QC โ€ข On-site

Full-time

Re-posted 3 days ago


Job description

Proposal Specialist

Are you a recent graduate or looking to take the next step in your career? CellCarta, a Contract Research Organization, is seeking a Proposal Specialist to join our dynamic team. In this role, you will support proposal development while collaborating with talented professionals dedicated to advancing human health. Apply today and take the first step toward an exciting career with CellCarta!

Summary

Reporting to the Associate Director, Client Services, the Proposal Specialist will prepare proposals and task orders, ensuring coordination and tracking through the client relationship management (CRM) system. Additionally, this role will work closely with the Commercial team, Client Managers, and relevant stakeholders in Operations.

Responsibilities

  • Develop and/or review proposals or statements of service for accuracy
  • Prepare sales price estimates for protocols, bid requests, study revisions, and additions using site-suggested selling prices
  • Update and maintain the CRM system to ensure proper tracking
  • Follow up with internal (and potentially external) stakeholders as needed to ensure proposals are complete and meet customer needs, as well as quality and regulatory requirements
  • Assist management in monitoring sales pricing practices to ensure accuracy and relevance to study type, service, and operational processes
  • Ensure all required legal documents are in place
  • Interact with scheduling or project management groups to identify the dates for studies or services and assist with scheduling, as required
  • Support responses to RFIs through coordination with local stakeholders
  • Maintain and update the tools and processes required to provide accurate proposals within a short timeframe, such as price lists, budgeting templates, and customer-specific agreements
  • Perform all other related duties as assigned

Education

  • Minimum bachelor’s degree in life sciences, applied sciences, business, or related field

Main Requirements

  • No prior experience is required; however, experience in histopathology, immunohistochemistry, and/or genomics, as well as in client services, budget preparation, or the use of a CRM system, would be considered an asset
  • Proficiency in French and English, spoken and written; the incumbent will be required to interact with colleagues outside Quebec and will be required to read and draft documentation in English, as required by industry regulations
  • Proficiency with Microsoft Office Suite (e.g., Word, Excel, PowerPoint, Outlook)
  • Strong teamwork and collaboration skills, with the ability to manage multiple priorities simultaneously while maintaining attention to detail

Working Conditions

  • Full-time position, with 2-3 days onsite per week. Candidates must be located in the Montreal area

What We Can Offer

  • Competitive Wages
  • Vacation and Personal Days
  • Comprehensive Group Insurance Plans
  • RRSP Contribution with Employer Matching
  • Employee Annual Incentive Plan (EAIP)
  • Dialogue Telemedicine Service and Employee Assistance Program (EAP)
  • Referral Program
  • Career Advancement Opportunities

About CellCarta

CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The Company operates globally with facilities located in Canada, USA, Belgium, Australia, and China.
Joining CellCarta means working with dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world! 
Join us as we make an impact on patient therapy!
 

The information collected to review your application will be processed by the human resources services of CellCarta Biosciences Inc. and its affiliates (collectively, “CellCarta”). The legal basis for this processing is the legitimate interest of CellCarta to evaluate the suitability of candidates for the roles available at CellCarta.

CellCarta will only process that information which is necessary to evaluate your application. This information includes identifying information such as your name, address, email address and phone number, as well as information about your education and professional experience, including previous positions and your CV. Such information is required for us to complete your applicant file, assess your suitability for the role and comply with applicable laws. CellCarta may obtain personal information from other sources, such as during reference, background, or employment checks, with your permission, and from third party sources such as recruitment and assessment sites or professional social media sites, in each case only if such information is relevant to reviewing your application. Your personal information will be retained only for so long as reasonably necessary and in accordance with applicable laws. This information will be processed confidentially and only accessed by those who have a need for the recruitment process. Please note that the information comprising your applicant file may be processed in a country that is not where you are located (for example, you might be in the European Economic Area or Québec, Canada, whereas your applicant file may be reviewed by CellCarta in the United States). If you are offered and accept employment with CellCarta Biosciences Inc. or one of its affiliates, the information collected will become part of your employment record. If you do not want us to retain your information, or want us to update it, please contact privacy@cellcarta.com.

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