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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 Summary As a Research Scientist Bioanalysis for our Bioanalysis team at our Senneville (Montreal West) site, you will be responsible for the design, conduct and reporting of Laboratory Sciences studies efficiently, profitably and with the maximum scientific quality. The Research Scientist scientifically directs the Analysts and other technical staff associated with the conduct, interpretation and reporting of studies. In this role, primary responsibilities include: • Design, write, review and edit, as necessary, study plans, amendments and study schedules that define and schedule all study activities. • Oversee and coordinate all aspects of study related Laboratory Sciences procedures, whether performed within the department or by service departments. • Ensure that projects are performed according to standard operating procedures (SOPs) and Good Laboratory Practice (GLP) regulations, and are aware of regulations published by the FDA, EPA, JMHW and OECD. • Write, review and edit, as necessary, stand-alone contributing Scientist draft and/or final reports that document all study related procedures and results. • Prompt verbal or written communications with Study Directors and/or Sponsors on study related business, and generate and distribute Client Interaction Reports (CIRs) in a timely manner. • Ensure the accuracy and completeness of project cost estimates. • Review and approve raw data. • Ensure that a safe working environment is maintained by staff through the observance of safety procedures, the use of protective clothing and equipment, and by the distribution of relevant safety information. Job Qualifications We are looking for the following minimum qualifications for this role: Ph.D., M.Sc. or B.Sc. in chemistry or a related discipline. Depending on educational background, prior experience in the field may not be necessary. Why Charles River ? Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage) Paid development training and annual conferences Employee and family assistance program Access to a doctor and various health professionals (telemedicine) 4 weeks’ vacation & 10 sick/personal days per year Free on-site gym On-site cafeteria 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 supported the development of 86% of the drugs approved by the FDA in 2021. Equal Employment Opportunity Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. 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 [email protected]. 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.

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 Summary As an Analyst for our Laboratory Sciences team located at the Senneville site, you will be responsible for completing technical tasks by following the guidelines of the study plans and Standard Operating Procedures (SOP) and respecting Best Practices Laboratory (GLP). In this role, responsibilities may include: Carry out technical activities as described in the procedures and study plans, while respecting Good Laboratory Practices (GLP). Check the availability and prepare all of the components required for laboratory activities (documentation, samples, solutions, materials, equipment, etc.). Compile appropriate data and submit it in a clear, readable and complete manner. Ensure technical understanding of your work and ensure the smooth running of studies by identifying potential problems, potential solutions and corrective measures to be made. Perform any other related tasks as assigned. Éléments Clés If you have the following qualifications, we will train you for the rest: Holder of a DEC in sciences (biotechnology, medical laboratory or equivalent) or an AEC or a BAC in sciences (immunology, biology, biochemistry) An equivalent combination of education and experience may be considered an acceptable substitute for the specific education and experience as listed above. Ability to work in a team, organizational skills and ability to adapt to changes. Autonomous, meticulous and detail-oriented. Reading comprehension in English is mandatory. Bilingualism in French and English is preferred Position specific information Location: Senneville, Free parking Schedule: weekday schedule, Monday to Friday 8 a.m. to 4:15 p.m. Permanent position from hire, full time 37.5 hours per week Salary: $23/hour Why Charles River Competitive benefits upon hire. We pay up to 85% of premiums (medical & dental coverage) Employee and family assistance program Access to a doctor and various health professionals at all times (telemedicine) 3 weeks of vacation and 5 days of personal leave Numerous organized social activities If you want to contribute to the well-being of our communities, not only across the country, but around the world, join the team, 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 supported the development of 86% of the drugs approved by the FDA in 2021. Equal Employment Opportunity Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. 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 [email protected]. 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.

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 Summary As an Analyst for our Molecular Biology team located at the Senneville site, you will perform sample analysis work in a laboratory environment, perform data analysis to determine if results meet expectations and record data in accordance with company policies and standards to meet quality and accuracy requirements The Molecular Biology Department mainly analyzes the biodistribution of vectors and cells used primarily for gene and cell therapy. In addition, the team is called upon to analyze the expression of several genes modulated following treatment. The goal of these analyses is to understand the mode of action of different drugs and to determine if they are effective. We work with pharmaceutical compounds that target several therapeutic areas, including oncology, inflammation, infectious diseases, ocular diseases, metabolism, and diseases of the cardiovascular, renal, respiratory and central nervous systems. In this role, responsibilities may include: Perform a variety of DNA and RNA purification assays as well as qPCR and RT-qPCR assays on platforms such as Quantstudio, QXone (ddPCR), Maxwell, Quantigen, and Nanostring. Perform method development, validation and sample analysis testing. Document and process analytical data according to GLP (Good Laboratory Practices) to maintain the company's high level of quality. Work in collaboration with scientific staff to optimize methods. Key Elements If you have the following qualifications, we will train you for the rest: DEC in Science (Biotechnology, Medical Laboratory or equivalent) or a BAC in Science (Immunology, Biology, Biochemistry or equivalent) Ability to work under time constraints, excellent organizational skills, and ability to adapt to change. Work with precision, pay attention to detail, and strive for quality work. Self-starter with a collaborative and positive attitude. Reading and writing English is required. Bilingualism is an asset. Role Specific Information Location: Senneville (Shuttle service from Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site) Free parking Schedule: Weekday schedule, Monday to Friday Permanent position as of the hiring, full time 37.5hrs per week Salary : $23/H Why Charles River? Competitive benefits upon hire. We pay up to 85% of premiums (medical & dental coverage) Employee and family assistance program 24/7 access to a doctor and various health care professionals (telemedicine) 3 weeks’ Vacation & 5 Personal day policy Numerous organized social activities If you want to contribute to the well-being of our communities, not only across the country, but around the world, join the team, 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 supported the development of 86% of the drugs approved by the FDA in 2021. Equal Employment Opportunity Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. 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 [email protected]. 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.

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 Summary As an Analyst for our Biomarkers team located at the Senneville site, you will participate in the analysis of biological characteristics used to assess disease progression, normal biological processes and pharmacological responses to a drug or mode of action. Our broad scientific expertise covers key toxicology indications and a variety of therapeutic areas including oncology, inflammation, immunology, infectious diseases, and diseases of the cardiovascular, renal, respiratory and central nervous systems. In this role, responsibilities may include: Perform sample analysis based on a variety of immunoassays and enzyme assays such as ELISA, Luminex, radioimmunonalysis, ECL, MSC technology, Simoa technology, and Simple Protein ELLA Oversee method development and perform validation and data analysis to determine if results are as expected, in compliance with Good Laboratory Practice (GLP). Key elements If you have the following qualifications, we will train you for the rest: Holder of a DEC in Science (Biotechnology, Medical Laboratory or equivalent) or a BAC in Science (Immunology, Biology, Biochemistry) Ability to work under time constraints, outstanding organizational skills and ability to adapt to changes. Autonomous, pay attention to details and strive to achieve quality work Reading comprehension in English is mandatory. Bilingualism in French and English is preferred Role Specific Information Location: Senneville (Shuttle service from Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site) Free parking Schedule: Weekday schedule, Monday to Friday Permanent position as of the hiring, full time 37.5hrs per week Why Charles River? Competitive benefits upon hire. We pay up to 85% of premiums (medical & dental coverage) Paid development training Employee and family assistance program 24/7 access to a doctor and various health care professionals (telemedicine) 3 weeks’ Vacation & 5 Personal day policy Numerous organized social activities If you want to contribute to the well-being of our communities, not only across the country, but around the world, join the team, 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 supported the development of 86% of the drugs approved by the FDA in 2021. Equal Employment Opportunity Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. 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 [email protected]. 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.