CA$75K/yr
Communicate proactively and effectively with the Study Director (SD), clients, and involved scientists (IS and/or PI); * Independently identify, analyze, and resolve issues related to production ...
CA$75K/yr
Communicate proactively and effectively with the Study Director (SD), clients, and involved scientists (IS and/or PI); * Independently identify, analyze, and resolve issues related to production ...
Job Overview As a Method Development Research Scientist (Large Molecule) for our Bioanalysis team at the Laval location, you will act as a Study Director responsible for the conduct of all analytical ...
Job Overview As a Method Development Research Scientist (Large Molecule) for our Bioanalysis team at the Laval location, you will act as a Study Director responsible for the conduct of all analytical ...
In this role, you will lead the skill development of Local Study Operations Managers (LSOM ... Experience managing multiple teams / direct reports across multiple clinical functions / trials
In this role, you will lead the skill development of Local Study Operations Managers (LSOM ... Experience managing multiple teams / direct reports across multiple clinical functions / trials
Acting as the primary Sponsor contact for Global CRO Project Directors and Global functional leads ... Ensuring studies adhere to regulatory requirements and ethical standards, handling regulatory ...
Acting as the primary Sponsor contact for Global CRO Project Directors and Global functional leads ... Ensuring studies adhere to regulatory requirements and ethical standards, handling regulatory ...
You have direct, hands-on experience managing clinical study start-up and site activation activities (strongly preferred) * You possess a strong working knowledge of ICH-GCP guidelines and Health ...
You have direct, hands-on experience managing clinical study start-up and site activation activities (strongly preferred) * You possess a strong working knowledge of ICH-GCP guidelines and Health ...
Prompt verbal or written communications with Study Directors and/or Sponsor on study related business in a timely manner; * Ensure the accuracy and completeness of project cost estimates; * Notify ...
Prompt verbal or written communications with Study Directors and/or Sponsor on study related business in a timely manner; * Ensure the accuracy and completeness of project cost estimates; * Notify ...
As needed, work with study directors to ensure data is accurately integrated into study reports; * Provide training, technical guidance and leadership to laboratory staff and may provide training ...
As needed, work with study directors to ensure data is accurately integrated into study reports; * Provide training, technical guidance and leadership to laboratory staff and may provide training ...
As needed, work with study directors to ensure data is accurately integrated into study reports; * Provide training, technical guidance and leadership to laboratory staff and may provide training ...
As needed, work with study directors to ensure data is accurately integrated into study reports; * Provide training, technical guidance and leadership to laboratory staff and may provide training ...
Centre Director - Iguarsivik School
CA$103K - CA$137K/yr
Under the supervision of the Assistant Director General, the Centre Director is the senior ... Undergraduate degree in a relevant field of study certifying a minimum three (3)-year university ...
Centre Director - Iguarsivik School
CA$103K - CA$137K/yr
Under the supervision of the Assistant Director General, the Centre Director is the senior ... Undergraduate degree in a relevant field of study certifying a minimum three (3)-year university ...
As an Associate Medical Director at Allucent, you are responsible for working independently to ... Identify study risks and provide input to the Risk plan * Review and understand study medical ...
As an Associate Medical Director at Allucent, you are responsible for working independently to ... Identify study risks and provide input to the Risk plan * Review and understand study medical ...
About the Role The Director, Finance is a high-impact, transformative leadership role overseeing a ... Candidates moving past initial screening will complete a practical case study and present their ...
About the Role The Director, Finance is a high-impact, transformative leadership role overseeing a ... Candidates moving past initial screening will complete a practical case study and present their ...
QC · On-site
$180 - $260/hr
About the Role The Director, Finance is a high-impact, transformative leadership role overseeing a ... Candidates moving past initial screening will complete a practical case study and present their ...
QC · On-site
$180 - $260/hr
About the Role The Director, Finance is a high-impact, transformative leadership role overseeing a ... Candidates moving past initial screening will complete a practical case study and present their ...
Director, Finance
Gatineau, QC · On-site
About the Role The Director, Finance is a high-impact, transformative leadership role overseeing a ... Candidates moving past initial screening will complete a practical case study and present their ...
Director, Finance
Gatineau, QC · On-site
About the Role The Director, Finance is a high-impact, transformative leadership role overseeing a ... Candidates moving past initial screening will complete a practical case study and present their ...
Under the supervision of the Director of Education Services and in collaboration with other ... Undergraduate degree in a relevant field of study certifying a minimum three-year university ...
Under the supervision of the Director of Education Services and in collaboration with other ... Undergraduate degree in a relevant field of study certifying a minimum three-year university ...
Directeur medical adjoint-Neurologie / Associate Medical Director-Neurology(CAN)
Montreal, QC · On-site
As an Associate Medical Director at Allucent, you are responsible for working independently to ... Identify study risks and provide input to the Risk plan * Review and understand study medical ...
Directeur medical adjoint-Neurologie / Associate Medical Director-Neurology(CAN)
Montreal, QC · On-site
As an Associate Medical Director at Allucent, you are responsible for working independently to ... Identify study risks and provide input to the Risk plan * Review and understand study medical ...
Food Service Director
CA$75K - CA$80K/yr
Reporting to the General Manager, the Food Service Director plays a key leadership role in ... studies. Career Growth: Clear career path planning and development opportunities tailored to your ...
Food Service Director
CA$75K - CA$80K/yr
Reporting to the General Manager, the Food Service Director plays a key leadership role in ... studies. Career Growth: Clear career path planning and development opportunities tailored to your ...
Product Director, Knowledge
Montreal, QC · On-site
As a Product Director, Knowledge at Ubisoft Montreal, you will guide the Knowledge stream within ... studies
Product Director, Knowledge
Montreal, QC · On-site
As a Product Director, Knowledge at Ubisoft Montreal, you will guide the Knowledge stream within ... studies
The Associate Director partners closely with sponsors and cross-functional teams to translate ... studies. * Develop and execute nonclinical regulatory strategies to support early-phase drug ...
The Associate Director partners closely with sponsors and cross-functional teams to translate ... studies. * Develop and execute nonclinical regulatory strategies to support early-phase drug ...
Associate Director, Regulatory Affairs & Submissions - Nonclinical Development
Montreal, QC · On-site
The Associate Director partners closely with sponsors and cross-functional teams to translate ... studies. * Develop and execute nonclinical regulatory strategies to support early-phase drug ...
Associate Director, Regulatory Affairs & Submissions - Nonclinical Development
Montreal, QC · On-site
The Associate Director partners closely with sponsors and cross-functional teams to translate ... studies. * Develop and execute nonclinical regulatory strategies to support early-phase drug ...
The GDL is a key partner for other clinical and clinical operations colleagues through the lifestyle of all studies for the assigned asset(s). The GDL may also act as a key partner to external ...
The GDL is a key partner for other clinical and clinical operations colleagues through the lifestyle of all studies for the assigned asset(s). The GDL may also act as a key partner to external ...
Study Director information
What is a study director?
A Study Director is the individual responsible for the overall conduct of a scientific study, particularly in regulated environments such as pharmaceuticals, chemicals, or environmental research. They oversee the planning, execution, and reporting of studies to ensure they comply with regulatory standards, such as Good Laboratory Practice (GLP). The Study Director acts as the main point of control and communication, coordinating among team members and ensuring that the study meets its scientific and regulatory objectives. Their role is critical for the integrity and quality of the data generated.
What does a study director do?
As a study director, your job is to manage studies, analyze results, and interpret reports so you can deliver a summary of the findings. This work has three categories. First, on the technical side, your job includes creating the plan for the study, coordinating with other scientists, and overseeing data collection. In the administrative role, you monitor junior employees and ensure each investigation finishes within budgetary constraints. In the compliance role, you ensure that each study happens under strict safety and ethics protocols. You may be asked to run multiple studies at the same time, adding to the complexity of this position.
How does a study director typically collaborate with cross-functional teams during a research project?
As a Study Director, you play a central role in coordinating research activities by regularly collaborating with scientists, technicians, quality assurance personnel, and regulatory teams. You are responsible for ensuring all team members are aligned on study objectives, timelines, and compliance requirements. Effective communication and leadership are essential, as you facilitate meetings, delegate tasks, and resolve issues that arise to keep the project on track. This collaborative environment not only fosters professional growth but also provides valuable exposure to various scientific and operational domains within the organization.
What skills and qualifications does a successful study director have?
To thrive as a Study Director, you need a solid background in scientific research methods, regulatory compliance, and study protocol development, usually supported by an advanced degree in life sciences or a related field. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP) standards, and project management tools is highly valued. Strong leadership, attention to detail, and effective communication are crucial soft skills for managing cross-functional teams and ensuring study integrity. These competencies are vital to ensure regulatory adherence, data accuracy, and successful project outcomes in research environments.
What is the difference between Study Director vs Laboratory Manager?
| Aspect | Study Director | Laboratory Manager |
|---|---|---|
| Credentials | Typically requires advanced degrees (e.g., MS, PhD) and relevant certifications | Requires relevant degrees and management experience, but not necessarily advanced research credentials |
| Work Environment | Leads specific research or regulatory studies, often in contract labs or pharmaceutical companies | Oversees daily lab operations, staff, and compliance across multiple projects |
| Industry Usage | Commonly used in GLP, clinical, and research settings | Used broadly in laboratory settings across industries |
The Study Director focuses on designing, overseeing, and ensuring the integrity of specific studies, often requiring scientific expertise. The Laboratory Manager handles overall lab operations, staff management, and compliance. Both roles are essential but differ in scope and responsibilities.
More about Study Director jobs
What are the most commonly searched types of Study jobs in Quebec?
The most popular types of Study jobs in Quebec are:
CA$75K/yr
Full-time
Medical, Retirement, PTO
Re-posted yesterday
Charles River Laboratories rating
8.3
Based on 95 frontline employees who took The Breakroom Quiz
23rd of 86 rated pharmaceutical
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
As an Associate for our Pharmacokinetics team at the Senneville location, you will be responsible for the entire pharmacokinetic (PK) analysis process, including the communication of results within the context of preclinical studies.
In this role, primary responsibilities include:
- Gather and consolidate relevant information related to pharmacokinetics (PK) and toxicokinetics (TK) studies;
- Review and draft study plans/protocols for PK and TK studies, including amendments and preparation of PK/TK phase plans;
- Perform data tabulation, conduct preliminary analyses, and generate summary results while demonstrating a strong understanding of PK processes and timelines;
- Conduct pharmacokinetic analyses (non-compartmental analysis), interpret results, and prepare associated scientific reports;
- Independently use PK platform tools, including Phoenix, PK Assist, and Integral.
- Communicate proactively and effectively with the Study Director (SD), clients, and involved scientists (IS and/or PI);
- Independently identify, analyze, and resolve issues related to production activities and scientific methodologies, in collaboration with the PK team;
- Perform quality control (QC) review of PK/TK data, analysis and reports to ensure accuracy and compliance;
- Maintain active scientific awareness in pharmacokinetics, including literature review and integration of relevant advancements, as well as proficiency with analysis software (e.g., WinNonlin and other PK parameter estimation tools).
Key Elements
We are looking for the following minimum qualifications for this role:
- Baccalaureate in science or other advanced degrees preferred;
- A minimum of 2 years’ experience as PK associate;
- Proficient in performing non-compartmental analysis (NCA) using the PK modeling and analysis platforms; Phoenix WinNonlin and PK Assist (mandatory);
- Experienced with ‘Integral’ for data integration, study management, and PK/TK data review;
- Proficiency in French and English, both spoken and written.
Role Specific Information:
- Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
- Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
- Salary: $75,000 annually;
- Schedule: Monday-Friday with possible weekends when needed;
- Permanent position as of the hiring, full-time 37.5hrs per week.
Why Charles River ?
- We offer competitive benefits and advantages from day one to support your well-being;
- 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 & 10 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.
Contact information: annabelle.landry@crl.com / (438) 469 – 8575
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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About Charles River
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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 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 supported the development of 86% of the drugs approved by the FDA in 2021.
Industry
Scientific research and development services
Company size
10,000+ Employees
Headquarters location
Wilmington, MA, US
Year founded
1947