Syneos Health is a leading biopharmaceutical solutions organization that accelerates customer success through integrated clinical, medical, and commercial insights to improve patient outcomes.
Morrisville, NC
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, commercial and real world insights into outcomes to address modern market realities. We bring together a talented team of professionals with a deep understanding of patient and physician behaviors and market dynamics. Together we share diverse insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. Syneos Health is powered by an authentic, inclusive and high-performance culture that cares for colleagues, customers, patients, communities and the environment.
On-site · Québec
The role involves managing the receipt, inventory, storage, and disposal of clinical study samples and reagents. Additionally, the specialist will maintain storage equipment and ensure the integrity of materials through proper documentation and monitoring.
On-site · Québec
The senior reporting associate is responsible for drafting regulated documents and preparing data tables for validations and studies. They must also verify the quality of reports and support internal and external client requests.
On-site · Québec
The project supervisor is responsible for coordinating all bioanalytical project activities to meet client expectations while guiding the technical team. They also manage project resources, timelines, and ensure compliance with standard operating procedures and company policies.
On-site · Québec
The Project Supervisor is responsible for coordinating all bioanalytical activities for clinical research projects while guiding and mobilizing the technical team. They ensure project timelines are met, manage laboratory operations, and provide technical expertise to support the principal investigator.
Remote · Canada, Poland
The Clinical Data Reviewer performs specialized clinical data reviews ahead of significant project milestones to ensure data readiness and validity. They work as an extension of the clinical scientist to identify inconsistencies, highlight errors, and manage queries across large, multi-faceted data sets.
On-site · Québec
The clinical laboratory technician will perform and supervise general study protocol tasks such as vital signs, ECGs, and biological sample processing. They are also responsible for maintaining laboratory equipment, managing supplies, and supporting the training of other staff members.
On-site · Québec
The scientist will process, review, and evaluate chromatographic data while ensuring the accuracy of raw data and electronic transfers. They will also communicate findings to study management and assist in the training of new employees.
On-site · Québec
The research nurse will manage daily study protocols, ensure compliance with standard operating procedures, and maintain accurate clinical documentation. They will also coordinate participant visits, administer study medications, and report adverse events to the project management team.
On-site · Québec
The role involves ensuring the safety and well-being of clinical study subjects while adhering to study protocols and timelines. Responsibilities include performing technical clinical tasks such as venipuncture, administering medication, and monitoring physiological data.
On-site · Québec
The role involves ensuring the safety and well-being of clinical study subjects while performing technical tasks such as vital signs monitoring, venipuncture, and medication administration. The incumbent is also responsible for adhering to study protocols, managing study timelines, and ensuring informed consent procedures are correctly followed.
On-site · Québec
The clinical laboratory technician is responsible for applying professional techniques and procedures within the clinical laboratory unit while adhering to study timelines. Duties include performing clinical tasks such as vital signs, ECGs, sample collection, and equipment maintenance to support drug development studies.
On-site
Scientifique Analytique I - Future roles (Quebec) Syneos Health® est une organisation de premier plan, entièrement intégrée, spécialisée dans les services en sciences de la vie, conçue pour accélérer le succès de ses clients. Nous collaborons avec des innovateurs à chaque étape du continuum du développement et de la commercialisation des médicaments, en les aidant à naviguer dans la complexité, à anticiper le changement et à accélérer leurs progrès. Chaque jour, nous améliorons nos performances grâce à notre façon de travailler ensemble, comme une seule équipe, chacun étant expert dans son d…
On-site
Infirmière Auxiliaire - Future Roles (Quebec) Syneos Health® est une organisation de premier plan, entièrement intégrée, spécialisée dans les services en sciences de la vie, conçue pour accélérer le succès de ses clients. Nous collaborons avec des innovateurs à chaque étape du continuum du développement et de la commercialisation des médicaments, en les aidant à naviguer dans la complexité, à anticiper le changement et à accélérer leurs progrès. Chaque jour, nous améliorons nos performances grâce à notre façon de travailler ensemble, comme une seule équipe, chacun étant expert dans son domai…
Remote
Sponsor Dedicated Protocol Medical Writer II/Sr - US/Canada Remote Based Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you…
On-site · Québec
The Senior Report Associate is responsible for preparing data tables and regulatory reports for validations and studies within specific scientific disciplines. They also ensure quality control of reports and provide support for internal and external client requests.
Remote · Montreal, Quebec, Canada
The Site Activation Specialist II oversees the end-to-end site activation process at the country level, ensuring compliance with regulatory requirements and project timelines. They manage central and local regulatory submissions, facilitate communication between investigational sites and functional leads, and support budget and contract negotiations.
Remote · Toronto, Ontario, Canada
The Senior Director is responsible for driving sales growth across a geographic territory by balancing new client acquisition with the expansion of existing accounts. They lead multi-functional solution development and maintain strong relationships with key stakeholders to maximize territory performance.
Remote · Missouri, United States
Leads the preparation and completion of complex clinical medical writing deliverables while ensuring scientific accuracy and regulatory compliance. Coordinates cross-functional activities and mentors junior staff to ensure projects are delivered on time and within budget.
On-site · Québec
The Principal Investigator is responsible for managing bioanalytical projects, overseeing laboratory activities, and ensuring compliance with regulatory standards. They act as the primary liaison for clients, manage project budgets, and provide technical guidance to the laboratory team.
Remote · United States
Execute commercial lifecycle management strategies and regulatory submissions with a focus on US, Canada, and EU markets. Participate in cross-functional teams and serve as the primary regulatory CMC contact for assigned products.
