Current jobs related to Study Start Up Associate Ii - Montreal, Quebec - ICON
-
Site Start-Up
3 weeks ago
Montreal, Quebec, Canada Syneos Health Full timeAbout the RoleSyneos Health is a leading biopharmaceutical solutions organization that accelerates customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.As a Regulatory Specialist II - Clinical Trial Start-Up, you will play a critical role in ensuring the quality of our...
-
Site Start-Up
3 weeks ago
Montreal, Quebec, Canada Syneos Health Full timeAbout the RoleSyneos Health is a leading biopharmaceutical solutions organization that accelerates customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.As a Regulatory Specialist II - Clinical Trial Start-Up, you will play a critical role in ensuring the quality of our...
-
Regulatory Specialist II
3 weeks ago
Montreal, Quebec, Canada Syneos Health Full timeAbout the RoleSyneos Health is a leading biopharmaceutical solutions organization that accelerates customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.As a Regulatory Specialist II - Clinical Trial Start-Up, you will play a critical role in ensuring the quality of our...
-
Regulatory Specialist II
3 weeks ago
Montreal, Quebec, Canada Syneos Health Full timeAbout the RoleSyneos Health is a leading biopharmaceutical solutions organization that accelerates customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.As a Regulatory Specialist II - Clinical Trial Start-Up, you will play a critical role in ensuring the quality of our...
-
Site Start-Up
1 week ago
Montreal, Quebec, Canada Syneos Health Full timeSyneos Health is a leading fully integrated biopharmaceutical solutions organization. We accelerate customer success by translating unique clinical, medical affairs, and commercial insights into outcomes. As a Site Start-Up & Regulatory Specialist II, you will play a key role in ensuring compliance with regulatory requirements and facilitating site...
-
Site Start-Up
1 week ago
Montreal, Quebec, Canada Syneos Health Full timeSyneos Health is a leading fully integrated biopharmaceutical solutions organization. We accelerate customer success by translating unique clinical, medical affairs, and commercial insights into outcomes. As a Site Start-Up & Regulatory Specialist II, you will play a key role in ensuring compliance with regulatory requirements and facilitating site...
-
Site Start-Up
1 week ago
Montreal, Quebec, Canada Syneos Health Full timeSyneos Health is a leading fully integrated biopharmaceutical solutions organization. We accelerate customer success by translating unique clinical, medical affairs, and commercial insights into outcomes. As a Site Start-Up & Regulatory Specialist II, you will play a key role in ensuring compliance and efficiency in our hybrid schedule. Your expertise will...
-
Site Start-Up
1 week ago
Montreal, Quebec, Canada Syneos Health Full timeSyneos Health is a leading fully integrated biopharmaceutical solutions organization. We accelerate customer success by translating unique clinical, medical affairs, and commercial insights into outcomes. As a Site Start-Up & Regulatory Specialist II, you will play a key role in ensuring compliance and efficiency in our hybrid schedule. Your expertise will...
-
Montreal, Quebec, Canada Precision Medicine Group Full timeAbout UsPrecision Medicine Group is a precision medicine CRO that combines innovative clinical trial designs, operational expertise, and advanced data analytics to deliver robust insights for complex disease states.We are passionate about supporting professional growth and are proud to share extremely high CRA retention rates compared to industry...
-
Montreal, Quebec, Canada Precision Medicine Group Full timeAbout UsPrecision Medicine Group is a precision medicine CRO that combines innovative clinical trial designs, operational expertise, and advanced data analytics to deliver robust insights for complex disease states.We are passionate about supporting professional growth and are proud to share extremely high CRA retention rates compared to industry...
-
Montreal, Quebec, Canada Precision Medicine Group Full timeAbout UsPrecision Medicine Group is a precision medicine CRO that combines innovative clinical trial designs, operational and medical expertise, advanced biomarker and data analytics solutions, and a passion for complex disease states.We are dedicated to supporting professional growth and are proud to share extremely high CRA retention rates compared to...
-
Montreal, Quebec, Canada Precision Medicine Group Full timeAbout UsPrecision Medicine Group is a precision medicine CRO that combines innovative clinical trial designs, operational and medical expertise, advanced biomarker and data analytics solutions, and a passion for complex disease states.We are dedicated to supporting professional growth and are proud to share extremely high CRA retention rates compared to...
-
Site Start-Up and Regulatory Specialist II
2 weeks ago
Montreal, Quebec, Canada Syneos Health Full timeAbout the RoleWe are seeking a highly skilled Site Start-Up and Regulatory Specialist II to join our team at Syneos Health. As a key member of our organization, you will be responsible for ensuring the successful start-up and operation of clinical trial sites.Key ResponsibilitiesDevelop and implement site start-up strategies to ensure timely and efficient...
-
Site Start-Up and Regulatory Specialist II
3 weeks ago
Montreal, Quebec, Canada Syneos Health Full timeAbout the RoleWe are seeking a highly skilled Site Start-Up and Regulatory Specialist II to join our team at Syneos Health. As a key member of our organization, you will be responsible for ensuring the successful start-up and operation of clinical trial sites.Key ResponsibilitiesDevelop and implement site start-up strategies to ensure timely and efficient...
-
Montreal, Quebec, Canada Precision Medicine Group Full timeAbout UsPrecision Medicine Group is a precision medicine Contract Research Organization (CRO) that combines innovative clinical trial designs, operational expertise, and advanced data analytics to deliver robust insights that inform real-time decisions.Job SummaryWe are seeking a Clinical Research Associate II/Sr. Clinical Research Associate to join our...
-
Montreal, Quebec, Canada Precision Medicine Group Full timeAbout UsPrecision Medicine Group is a precision medicine Contract Research Organization (CRO) that combines innovative clinical trial designs, operational expertise, and advanced data analytics to deliver robust insights that inform real-time decisions.Job SummaryWe are seeking a Clinical Research Associate II/Sr. Clinical Research Associate to join our...
-
Montreal, Quebec, Canada Precision Medicine Group Full timeAbout UsPrecision Medicine Group is a precision medicine Contract Research Organization (CRO). We are passionate about supporting professional growth and are proud to share extremely high Clinical Research Associate (CRA) retention rates compared to industry averages.Our team is dedicated to delivering exceptional results and creating a positive work...
-
Montreal, Quebec, Canada Precision Medicine Group Full timeAbout UsPrecision Medicine Group is a precision medicine Contract Research Organization (CRO). We are passionate about supporting professional growth and are proud to share extremely high Clinical Research Associate (CRA) retention rates compared to industry averages.Our team is dedicated to delivering exceptional results and creating a positive work...
-
Clinical Research Associate II
1 month ago
Montreal, Quebec, Canada 405 ICR Canada - CAN Full timeClinical Research Associate II - French ProficientLocation: Canada, MontrealEmployment Type: Full-timeJob ID: JR119531At 405 ICR Canada, our workforce is our greatest asset. Our diverse teams empower us to enhance our partnerships with clients and contribute to our mission of advancing patient care.Our culture is founded on four core values that unite us as...
-
Regulatory Specialist II
4 days ago
Montreal, Quebec, Canada Syneos Health Full timeJob Title: SSU & Regulatory Specialist IIAbout the RoleWe are seeking a highly skilled SSU & Regulatory Specialist II to join our team at Syneos Health. As a key member of our team, you will be responsible for ensuring the quality of our clinical trial start-up processes and regulatory compliance.Key ResponsibilitiesEnsure quality deliverables at the country...
Study Start Up Associate Ii
3 months ago
With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
Study Start Up Associate II - French speaking/office based
Must be proficient with the French language - verbal and written communication
**The Role**:
As a member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices.
- Coordinate, balance and facilitate activities related to the completion of Critical Document Package (CDP) and the IP release checklist (SST004-SOP-F01) in accordance with ICH GCP guidelines and all applicable regulations, laws, ethical standards, other guidelines, sponsor requirements
- Ensure that the overall process is focused on quality, efficiency and cost containment for a particular region / sub division within the CDP group, under the general mentorship of Mgr/Sr. Manager - Central Services or Designee.
**To be successful in the role, you will have**:
- A high school diploma or local equivalent
- Bachelor's Degree preferably in Life Sciences
- Minimum of 1 years' experience or understanding of clinical study start up requirements and activities.
- Experience of Clinical Trial operations and meeting regulatory guidelines
- Proficient project management skills.
**Benefits of Working in ICON**:
Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
**Annonce Assistant(e) de démarrage des études (SSUA) - Montréal**
ICON plc est un chef de file mondial en matière de soins de santé intelligents et de recherches cliniques. De la molécule au médicament, nous faisons progresser la recherche clinique en fournissant des services externalisés à des entreprises pharmaceutiques, biotechnologiques, de fabrication de dispositifs médicaux ainsi qu'à des organismes gouvernementaux et de santé publique.
Les patients étant au cœur de tout ce que nous faisons, nous contribuons à accélérer le développement de médicaments et de dispositifs qui sauve des vies et améliore la qualité de vie.
Nos employés constituent notre principal atout, sont l'essence de notre culture, et le moteur de notre réussite. Les employés de ICON ont pour mission de réussir et sont passionnés ce qui fait en sorte que ce que nous faisons, nous le faisons bien.
**Poste - ARC principal**
En tant que membre de l'équipe de mise en œuvre des études, vous jouerez un rôle essentiel pour ce qui est de vous assurer que les médecins de nos centres de recherche sont prêts à démarrer les essais de produits expérimentaux et de nouveaux produits pharmaceutiques ou biologiques pour les essais cliniques à leurs cabinets locaux.
- Coordonner, concilier et faciliter les activités liées à la finalisation des trousses des documents essentiels (CDP) et de la liste de vérification de publication du produit expérimental (SST004-SOP-F01) conformément aux directives ICH GCP et à toutes les réglementations, lois, normes éthiques, autres directives et exigences du promoteur applicables
- S'assurer que l'ensemble du processus met l'accent sur la qualité, l'efficacité et la limitation des coûts pour une région/sous-division en particulier dans le groupe CDP, sous la conduite générale du gestionnaire principal - Services centraux ou de la personne désignée.
**Pour réuss
