We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... Responsible for managing the research activities at sites participating in Worldwide's clinical ...
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... Responsible for managing the research activities at sites participating in Worldwide's clinical ...
Infirmier(ere) autorise(e) en essais cliniques - Registered Nurse - Clinical Trials
Trois-rivieres, QC · On-site
JOB SUMMARY The Specialty Pharma Nurse, Clinical Trials Registered Nurse (CTRN) reports directly to the Specialty Pharma Nurse Supervisor (SPNS) and/or Specialty Pharma Nurse Manager (SPNM). In this ...
Infirmier(ere) autorise(e) en essais cliniques - Registered Nurse - Clinical Trials
Trois-rivieres, QC · On-site
JOB SUMMARY The Specialty Pharma Nurse, Clinical Trials Registered Nurse (CTRN) reports directly to the Specialty Pharma Nurse Supervisor (SPNS) and/or Specialty Pharma Nurse Manager (SPNM). In this ...
Associate Director, Operations - Clinical Assessment Technologies (CAT) - US/Canada - Remote
Quebec, QC · Remote
At least 7+ years clinical trial experience with at least 4 years' experience in global clinical trials * Preferred at least 5+ years of experience managing team members or project management ...
Associate Director, Operations - Clinical Assessment Technologies (CAT) - US/Canada - Remote
Quebec, QC · Remote
At least 7+ years clinical trial experience with at least 4 years' experience in global clinical trials * Preferred at least 5+ years of experience managing team members or project management ...
Responsable des litiges en matière de responsabilité du fait des produits et de garantie / Produc...
CA$90K - CA$115K/yr
Conduct and lead small claims court proceedings and trials. Manage vehicle inspections from initial request to review of expert inspection report. Coordinate and assist with requested vehicle buy ...
Responsable des litiges en matière de responsabilité du fait des produits et de garantie / Produc...
CA$90K - CA$115K/yr
Conduct and lead small claims court proceedings and trials. Manage vehicle inspections from initial request to review of expert inspection report. Coordinate and assist with requested vehicle buy ...
Territory Sales Manager
Montreal, QC · On-site
$70K/yr
This role also plays an important part in product evaluation and field trials, helping identify ... Collaborate with the Sales Manager to strengthen the customer base, support existing growers, and ...
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Apply Early
Territory Sales Manager
Montreal, QC · On-site
$70K/yr
This role also plays an important part in product evaluation and field trials, helping identify ... Collaborate with the Sales Manager to strengthen the customer base, support existing growers, and ...
Apply Early
... clinical trials to bring life-changing therapies to patients in need across the globe. We are ... As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical ...
... clinical trials to bring life-changing therapies to patients in need across the globe. We are ... As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical ...
Account Manager
Quebec, QC · On-site
Build and manage direct relationships with operators to drive trials, menu placements, and product adoption. * Manage a personal pipeline of opportunities from prospecting through close. * Partner ...
Account Manager
Quebec, QC · On-site
Build and manage direct relationships with operators to drive trials, menu placements, and product adoption. * Manage a personal pipeline of opportunities from prospecting through close. * Partner ...
Build and manage direct relationships with operators to drive trials, menu placements, and product adoption. * Manage a personal pipeline of opportunities from prospecting through close. * Partner ...
Build and manage direct relationships with operators to drive trials, menu placements, and product adoption. * Manage a personal pipeline of opportunities from prospecting through close. * Partner ...
Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards. * Collaborate with cross-functional teams to establish and implement clinical trial ...
Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards. * Collaborate with cross-functional teams to establish and implement clinical trial ...
Mastery to present scientific data on product with clarity using promotional tools and approved clinical trials * Proven track record of promoting products and managing clients in a knowledge ...
Mastery to present scientific data on product with clarity using promotional tools and approved clinical trials * Proven track record of promoting products and managing clients in a knowledge ...
Mastery to present scientific data on product with clarity using promotional tools and approved clinical trials * Proven track record of promoting products and managing clients in a knowledge ...
Mastery to present scientific data on product with clarity using promotional tools and approved clinical trials * Proven track record of promoting products and managing clients in a knowledge ...
... trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You will take responsibility for contract management ...
... trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You will take responsibility for contract management ...
You will manage sales activities and identify customer needs to tailor effective solutions ... You will lead and coordinate campaigns and technical projects, including trials, demonstrations ...
You will manage sales activities and identify customer needs to tailor effective solutions ... You will lead and coordinate campaigns and technical projects, including trials, demonstrations ...
You will manage sales activities and identify customer needs to tailor effective solutions ... You will lead and coordinate campaigns and technical projects, including trials, demonstrations ...
You will manage sales activities and identify customer needs to tailor effective solutions ... You will lead and coordinate campaigns and technical projects, including trials, demonstrations ...
Account Manager - Outside Sales/New Business Development
Montreal, QC · On-site
CA$103K - CA$166K/yr
Coordinate plant/site visits, product trials, and technical consultations to accelerate deal cycles ... Use CRM to manage pipeline health, risk, and coverage; ensure data completeness and timeliness.
Account Manager - Outside Sales/New Business Development
Montreal, QC · On-site
CA$103K - CA$166K/yr
Coordinate plant/site visits, product trials, and technical consultations to accelerate deal cycles ... Use CRM to manage pipeline health, risk, and coverage; ensure data completeness and timeliness.
Project / Process Engineer
Montreal, QC · On-site
Conduct process trials, validation, and design of experiments (DOE) * Evaluate material behavior ... Ability to manage multiple projects * Strong communication and teamwork skills * Bilingualism ...
Quick apply
Apply Early
Project / Process Engineer
Montreal, QC · On-site
Conduct process trials, validation, and design of experiments (DOE) * Evaluate material behavior ... Ability to manage multiple projects * Strong communication and teamwork skills * Bilingualism ...
Apply Early
... clinical trials and respond to emergency situations based upon clinical research standards ... Responsible for all aspects of site management as prescribed in the project plans * General On-Site ...
... clinical trials and respond to emergency situations based upon clinical research standards ... Responsible for all aspects of site management as prescribed in the project plans * General On-Site ...
JOB SUMMARY The Specialty Pharma Nurse, Clinical Trials Registered Nurse (CTRN) reports directly to the Specialty Pharma Nurse Supervisor (SPNS) and/or Specialty Pharma Nurse Manager (SPNM). In this ...
JOB SUMMARY The Specialty Pharma Nurse, Clinical Trials Registered Nurse (CTRN) reports directly to the Specialty Pharma Nurse Supervisor (SPNS) and/or Specialty Pharma Nurse Manager (SPNM). In this ...
Cardiologist (strongly preferred)with cardiovascular outcome trials or large complex, global ... Management experience - Able to work ina highly complexmatrixed environment and able to influence ...
Cardiologist (strongly preferred)with cardiovascular outcome trials or large complex, global ... Management experience - Able to work ina highly complexmatrixed environment and able to influence ...
CRA 1/2 & Sr. CRAs - CAR-T - Oncology & General Medicine, French Speaking - Canada
Montreal, QC · Remote
... clinical trials and respond to emergency situations based upon clinical research standards ... Responsible for all aspects of site management as prescribed in the project plans * General On-Site ...
CRA 1/2 & Sr. CRAs - CAR-T - Oncology & General Medicine, French Speaking - Canada
Montreal, QC · Remote
... clinical trials and respond to emergency situations based upon clinical research standards ... Responsible for all aspects of site management as prescribed in the project plans * General On-Site ...
Trials Manager information
What are the key skills and qualifications needed to thrive as a Trials Manager, and why are they important?
What are Trials Managers?
What are the main challenges a Trials Manager faces when coordinating multi-site clinical trials?
What is the difference between Trials Manager vs Clinical Research Coordinator?
| Criteria | Trials Manager | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, experience in trial management, knowledge of regulations | Bachelor's degree, clinical research experience, regulatory knowledge |
| Work Environment | Oversees multiple trials, manages teams, coordinates with sponsors | Handles daily trial activities, patient interactions, data collection |
| Employer & Industry Usage | Pharmaceutical companies, CROs, biotech firms | Hospitals, clinics, research institutions |
The Trials Manager focuses on overseeing entire clinical trials, managing teams, and ensuring compliance across multiple studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, working directly with patients and collecting data. Both roles require similar educational backgrounds and regulatory knowledge but differ in scope and responsibilities.
Senior Clinical Research Associate - Oncology - Canada (Bilingual)
Quebec, QC • On-site
Full-time
Posted 15 days ago
Job description
Who we are
We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!
What Clinical Operations does at Worldwide
At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.
As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.
Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. We take pride in our accessible Executive Leadership team, who are equally committed to advancing science and surmounting obstacles to make a difference in the lives of patients around the world.
We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial. Experience a world of difference with us at Worldwide!
What you will do
Responsible for managing the research activities at sites participating in Worldwide's clinical research projects
Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded
Conduct study initiation visits (SIVs)
While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements
What you will bring to the role
Excellent interpersonal, oral, and written communication skills in English
Superior organizational skills with attention to detail
Ability to work with little or no supervision
Proficiency in Microsoft Office, CTMS, and EDC Systems
Your experience
5+ years of experience as a Clinical Research Associate
4-year universitydegree OR Nursing Degree
Experience in Oncology is required
Fluent in written and verbal English and French is required
Candidates must reside in Canada
Willingness to travel regionally required
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative,innovative,and successful. We'reon a mission to hire thevery bestand are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.
About Worldwide Clinical Trials
Sourced by ZipRecruiter
Industry
Scientific research and development services
Company size
10,000+ Employees
Headquarters location
Durham, NC, US
Year founded
1986