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Scientific Analyst - Clinical Research - City of Quebec

Healthcare & life sciences
Syneos HealthQuébec, Quebec, CanadaPosted 2026-09-04
Temps plein

Description

Description

  • Scientific Analyst - Clinical Research - City of Quebec

Syneos Health® is a leading, fully integrated organization specializing in life sciences services, designed to accelerate the success of its clients. We collaborate with innovators at every stage of the drug development and commercialization continuum, helping them navigate complexity, anticipate change, and accelerate progress.

Members of our Clinical Solutions team adopt a drug development-focused approach, leveraging their years of experience and deep expertise to fully understand client needs and reflect them in the solutions we design.

Whether you join us as a Functional Service Provider partner or in a full-service environment, you will collaborate with passionate problem-solvers, innovating as a team to help our clients achieve their goals. We are agile and driven by the desire to deliver — for one another, for our clients, and most importantly, for the patients who need it.

Discover what your 25,000 future colleagues already know:

Why Syneos Health

  • We are passionate about developing our employees, thanks to career advancement opportunities, engaged and caring management, technical and therapeutic training, as well as peer recognition and total compensation programs.
  • We are committed to building an inclusive culture, where everyone can be fully themselves. At the heart of this approach lies our raison d’être — *Driven to Deliver* — which reflects the passion of our employees to provide daily solutions capable of having a significant impact on patients' lives.
  • We are continuously building the company we all want to work for and with which our clients want to collaborate. Why? Because we know that by bringing together talents from around the world, we can shape the future of healthcare, create impact for our clients, and accelerate progress for the benefit of patients.

Job Responsibilities

  • Process, examine, and evaluate chromatograms using appropriate applications.
  • Track chromatographic results with the study lead and management.
  • Perform electronic data transfers from various acquisition systems.
  • Verify and evaluate raw data, ensuring the consistency of the event sequence.
  • Verify the accuracy of raw data included in various tables.
  • Ensure responses are obtained regarding observations and that appropriate corrections are made.
  • Communicate information to the study lead and management to ensure project progress.
  • Participate in the training of new employees.
  • May be called upon to prepare and review documents during regulatory agency visits.
  • Interpret analysis results and provide opinions to management and the study lead on data or tests to be performed to aid in the study's progress.
  • Verify various documents, reports, maintenance reports, and equipment logs.
  • Responsible for performing activities in accordance with company and division policies, standardized operating procedures, and applicable operation guides, and performing other tasks assigned by management.

Qualifications

  • College diploma or bachelor's degree in sciences or another appropriate field.
  • Other relevant certification may be considered acceptable. This criterion ensures that the job holder has sufficient technical skills to assume their role.
  • Must demonstrate computer proficiency, especially in the use of Microsoft Word and Excel, and analytical software.
  • Excellent communication, presentation, and delivery skills, both written and oral, and ability to inform, influence, convince, and persuade.
  • Experience in a regulatory context will be considered an asset.
  • English level: Understanding of various messages, verbal exchange on subjects related to tasks to be performed, and writing simple messages.
  • Discover Syneos Health

Over the past five years, we have collaborated on 94% of all new drugs approved by the FDA, 95% of products authorized by the EMA, as well as more than 200 studies conducted at 73,000 sites involving more than 675,000 patients.

No matter your role, you will demonstrate initiative and challenge the status quo with us, in a highly competitive and ever-evolving environment. To learn more about Syneos Health: Additional Information

The tasks, functions, and responsibilities described in this job posting are not exhaustive. The company reserves the right, at its sole discretion and without notice, to assign other tasks, functions, and responsibilities. Equivalent experience, skills, and/or training will also be considered; therefore, the qualifications of job holders may differ from those indicated in this description. The company will determine, at its sole discretion, what constitutes equivalence to the qualifications mentioned above.

Furthermore, no provision of this document should be interpreted as creating an employment contract. The required skills and experiences may sometimes be described briefly. The content of this document aims to fully comply with the legal obligations applicable in each country where the company operates, including the implementation of the European directive on equal opportunities in recruitment and employment.

The company is committed to complying with the Americans with Disabilities Act (ADA), including providing reasonable accommodations, when appropriate, to help employees or candidates perform the essential functions of the job.

This posting was aggregated from linkedin. Groupe Sentinella is not the employer; applying takes you to the original site. The full text belongs to the original poster.

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Scientifique en analyse des résultats - Recherche Clinique - Ville de Québec — Groupe Sentinella