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Study Coordinator Jobs in Quebec (NOW HIRING)

This includes initial proposal development as well as updates driven by study design changes ... The Proposal Coordinator acts as a central point of coordination between Business Development ...

... a study coordinator or nursing role * 1+ years of clinical monitoring experience or equivalent combination of education and experience is required for the level 2 role; 3+ years is required for a ...

... a study coordinator or nursing role * 1+ years of clinical monitoring experience or equivalent combination of education and experience is required for the level 2 role; 3+ years is required for a ...

... studies of building a new railway line, increasing the capacity of the existing infrastructure ... The building coordinator will provide support to interface management across disciplines and ...

Coordinating with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation. * Maintaining accurate and up-to-date records of regulatory submissions and ...

... studies of building a new railway line, increasing the capacity of the existing infrastructure ... The Technical Specifications Coordinator will act as the central focal point for technical ...

We are looking for a nursing assistant coordinator for one of our semi-autonomous residences. The ... Diploma of professional studies (DEP) in health, assistance and nursing Formation of PDSB Up-to ...

... studies of building a new railway line, increasing the capacity of the existing infrastructure ... Participate in impact assessments by coordinating and/or contributing to multiple environmental ...

... studies of building a new railway line, increasing the capacity of the existing infrastructure ... Coordinating the collection of information from the team to consolidate clear, structured reporting ...

About The Role The Contracts Coordinator is responsible for the generation of all company-wide ... The requirement to have study protocols, designs and clinical research documents written and ...

... studies of building a new railway line, increasing the capacity of the existing infrastructure ... The Field Survey Coordinator will provide field coordination, oversight, and quality control ...

Junior Project Coordinator The position is based in Québec City. Your work with us: * Coordinate ... A DEC (Diploma of College Studies) or AEC (Attestation of College Studies) in Administration ...

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Showing results 1-20

Study Coordinator information

See Quebec salary details

$11

$26

$42

How much do study coordinator jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for study coordinator in Quebec is $26.87, according to ZipRecruiter salary data. Most workers in this role earn between $21.63 and $30.05 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Study Coordinator, and why are they important?

To thrive as a Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, usually backed by a bachelor’s degree in a science or health-related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, attention to detail, and effective communication help you manage study logistics and collaborate with research teams and participants. These skills ensure that studies are conducted ethically, efficiently, and in accordance with regulatory standards.

What Is a Study Coordinator?

A study coordinator works in a clinical research environment. In this position, your job duties are to oversee the day-to-day operations of a given study under the guidance of a research director. You direct tests, ensure all research is done according to ethical standards, and ensure the comfort and safety of subjects. As a study coordinator, you also ensure all patients provide informed consent prior to participation. Overall, your responsibility is to provide a safe environment for the study. To be a study coordinator, the qualifications are usually a bachelor’s degree or an RN degree. You typically need several years of experience in a clinical setting, and you must demonstrate skills in research.

How much does a CRC make?

In Ohio, a Clinical Research Coordinator (CRC) typically earns between $45,000 and $65,000 annually, depending on experience, certifications, and the employer. Entry-level CRCs may start at lower salaries, while those with specialized skills or certifications can earn higher wages. The role often requires knowledge of regulatory compliance and data management tools.

What is a study coordinator?

A study coordinator is a professional responsible for managing and overseeing clinical research studies or trials. They coordinate activities such as participant recruitment, data collection, and compliance with protocols, often working closely with researchers and healthcare providers. Strong organizational skills and knowledge of regulatory requirements are essential for this role.

What are study coordinators?

Study coordinators are professionals who manage the day-to-day operations of clinical research studies. They are responsible for tasks such as recruiting participants, ensuring protocol compliance, collecting and managing data, and maintaining communication between investigators, participants, and regulatory bodies. Study coordinators play a vital role in making sure that research studies are conducted ethically, efficiently, and according to regulatory guidelines. Their work ensures the integrity of study data and the safety of participants throughout the research process.

What are some common challenges Study Coordinators face when managing multiple clinical trials simultaneously?

Study Coordinators often juggle several clinical trials at once, each with its own protocols, timelines, and regulatory requirements. Keeping track of participant enrollment, data collection, and compliance across different studies can be demanding and requires strong organizational skills. Effective communication with investigators, sponsors, and other team members is crucial to prevent errors, ensure deadlines are met, and maintain the quality of study data. Using robust tracking systems and prioritizing tasks can help manage these challenges efficiently.

What is the difference between Study Coordinator vs Research Assistant?

AspectStudy CoordinatorResearch Assistant
Required CredentialsTypically a bachelor's degree in health sciences, biology, or related fieldOften a bachelor's degree or current student in a related field
Work EnvironmentClinical research settings, hospitals, or research institutionsLaboratories, research centers, or clinical sites
Employer & Industry UsageUsed by hospitals, universities, and research organizationsCommonly employed in academic and research institutions
Common Search & Comparison IntentUnderstanding roles, responsibilities, and qualificationsLearning about entry-level research roles and support tasks

The Study Coordinator and Research Assistant roles share similarities in working within research environments and requiring related educational backgrounds. However, Study Coordinators typically have more responsibilities in managing study protocols and participant coordination, while Research Assistants focus on supporting research activities and data collection. Both roles are essential in advancing clinical research and often work closely together in research projects.

How much does a study coordinator earn?

A study coordinator's average salary varies by experience and location but typically ranges from $45,000 to $70,000 annually. Entry-level coordinators may earn around $40,000, while those with more experience or specialized skills can earn over $80,000. The role often requires knowledge of clinical research protocols and data management tools.

Is CRC an entry level position?

A Clinical Research Coordinator (CRC) is often considered an entry-level position in clinical research, suitable for individuals with a bachelor's degree in a related field. However, some employers may prefer candidates with prior experience or certifications such as the Certified Clinical Research Coordinator (CCRC).
What are the most commonly searched types of Study jobs in Quebec? The most popular types of Study jobs in Quebec are:
What are popular job titles related to Study Coordinator jobs in Quebec? For Study Coordinator jobs in Quebec, the most frequently searched job titles are:
What job categories do people searching Study Coordinator jobs in Quebec look for? The top searched job categories for Study Coordinator jobs in Quebec are:
Infographic showing various Study Coordinator job openings in Quebec as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $55,884 per year, or $26.9 per hour.
Proposals Coordinator

Proposals Coordinator

Altasciences

Laval, QC • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 9 days ago


Altasciences rating

7.6

Company rating: 7.6 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

60th of 120 rated laboratories


Job description

Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.

We are better together and together We Are Altasciences.

About The Role
The Proposal Coordinator is responsible for managing the end-to-end preparation and coordination of bioanalytical quotes. This includes initial proposal development as well as updates driven by study design changes, amendments, and change orders. This role ensures that all scientific, operational, and financial inputs are accurately compiled, formatted, and delivered to support timely and competitive client deliverables. The Proposal Coordinator acts as a central point of coordination between Business Development, Client Management and Scientific Evaluators. Additional administrative tasks as assigned.

What You'll Do Here

Proposal & Quote Preparation

  • Coordinate the preparation of bioanalytical quotations based on inputs from Scientific Evaluators and Subject Matter Experts (SMEs).
  • Compile and format quote documents using available templates.
  • Ensure consistency, accuracy, and completeness of all quotation materials (Excel costing files, PDFs, and supporting documents).

Opportunity Management

  • Create, update, and manage opportunities within internal systems (e.g., Salesforce or equivalent).
  • Maintain accurate records of quote status, documentation, and version control.
  • Move opportunities through defined stages (e.g., "Proposal Complete") in alignment with process.

Quote Updates & Change Management

  • Manage updates to existing quotes resulting from study design changes, protocol amendments, or client-driven revisions.
  • Coordinate and implement change orders, ensuring all scientific and financial impacts are accurately reflected.
  • Collaborate with Scientific Evaluators to reassess scope, assumptions, and pricing as needed.
  • Maintain version control and ensure clear documentation of all revisions and change history requirements.

Cross-Functional Coordination

  • Act as the primary liaison between Business Development (BD), Scientific Evaluators, and other Costing teams.
  • Ensure all required inputs (both for initial proposals and subsequent updates) are received, validated, and incorporated.
  • Proactively follow up with internal stakeholders to meet timelines, especially for urgent amendments or change orders.

Documentation & Communication

  • Distribute finalized and/ or revised quotes (Excel and PDF) to BD and other Costing teams with all relevant details.
  • Ensure inclusion of key information such as internal/external assumptions and material cost breakdowns.
  • Maintain organized records of quote documentation for traceability purposes in required folders.

Process Compliance & Tracking

  • Follow established workflows and job aids for quotation generation and submission.
  • Track quotation progress using internal tools (e.g., SharePoint tracker or Salesforce) on a daily basis.
  • Ensure adherence to timelines, quality standards, and internal procedures.

Continuous Improvement

  • Identify opportunities to improve quotations templates, change order workflows, and coordination processes.
  • Support standardization of amendment and revision practices across the organization.
  • Contribute to improving turnaround times and operational efficiency.

Strategic Partnership

  • Following confirmation of strategic account BD assignments, Proposal Coordinators will be assigned to process new quotes and change orders for these accounts.
  • They will also attend regular meetings led by the Strategic Account BD or Partnership Manager to discuss and address feedback on proposals/CO process and format and will document the same in Ask Albert.

Perform any other duties as required.

What You'll Need to Succeed

  • BA/BS specializing in business or sciences. An equivalent combination of education and experience may be accepted.
  • 2-5 years' related experience in proposal coordination, project coordination, or similar roles with training in the biotech, pharmaceutical or CRO industry.
  • Experience with assay development, validation, or sample analysis is an asset.
  • Experience working with cross-functional teams and managing multiple deliverables.
  • Microsoft Office's suite of programs including: Word, Excel, and Internet Explorer. Familiarity with CRM systems (e.g., Salesforce) and document management tools.
  • Bilingual proficiency in French may be required, depending on location.
  • Ability to read and interpret study documents such protocol, study designs, method SOPs, etc.
  • Strong organizational and project coordination skills.
  • High attention to detail and accuracy in document preparation.
  • Ability to manage multiple conflicting priorities and meet tight deadlines
  • Excellent verbal and written communication skills.
  • Developed interpersonal skills are required.
  • Brings logical resolutions to conflicting interests and priorities.

Altasciences strives to provide a French work environment for its employees in Quebec. Altasciences has taken all reasonable measures to avoid imposing the above language requirement.

This requirement is essential for the position of Proposal Coordinator in particular, but without limitation, for the following reason(s):

  • The requirement to have study protocols read and documented in English as required by industry regulatory agencies

What We Offer:

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

Altasciences' Benefits Package Includes:

  • Health/Dental/Vision Insurance Plans
  • 401(k)/RRSP with Employer Match
  • Paid Vacation and Holidays
  • Paid Sick and Bereavement Leave
  • Employee Assistance & Telehealth Programs

Altasciences' Incentive Programs Include:

  • Training & Development Programs
  • Employee Referral Bonus Program
  • Annual Performance Review

#LI-MB1

MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH

Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!


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