Clinical Investigator
3 days ago
Your New Company
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.
We are better together and together We Are Altasciences.
About The Role
The Clinical Investigator (MD) is responsible for overseeing and delegating tasks related to the clinical trial under their leadership. The Clinical Investigator (MD) ensures the trial is conducted in accordance with Good Clinical Practice (GCP) by adhering to the study protocol, protecting participant rights and welfare, maintaining data integrity, and ensuring compliance with all applicable regulations, guidelines, and standard operating procedures (SOPs).
What You'll Do Here
Oversee all clinical activities related to the clinical trials for which they serve as Principal Investigator.
Ensure subject eligibility is met based on protocol inclusionary/exclusionary criteria and that the subject continues to meet eligibility criteria throughout the course of a clinical trial.
Perform physical examinations and medical history intake and review.
Ensure subject safety at all times, this may include but is not limited to: review of clinical laboratory results and/or other test results. Review and/or performance of vital signs, ECGs or other safety tests.
Record and follow-up on adverse events and determine causality.
Report serious adverse events to appropriate parties.
Be on-site for surveillance as required by protocol and remain available on-call for medical events.
Perform critical trial related tasks and/or make trial related decisions during the course of the trial.
Delegation of trial related tasks and the review of employees on the Delegation of Authority and Signature Log per job title/training record.
Perform protocol training.
Provide documentation for the Sub-Investigators.
Ensure requirements related to obtaining informed consent are met.
Participate in sponsor visits and regulatory audits.
Document study related events incompliance with GCP.
Complete and/or review regulatory documents as applicable.
Review study protocols and SOPs.
May act as Sub-Investigator on studies not assigned to them as Principal Investigator.
What You'll Need to Succeed
Required to have an active medical license from the Collège des médecins du Québec
Required to have a current ACLS certification card.
Excellent communication skills in French and English.
Previous experience with similar responsibilities; ideally related to the industry an asset.
Altasciences strives to provide a French working environment for its employees in Quebec. Although as part of its francization program has taken all reasonable steps to avoid imposing the above-mentioned requirement. Fluency in English is an essential requirement for the position of Clinical Investigator (MD) including, but not limited to, for the following reasons:
The requirement to have study protocols, designs and clinical research documents written and documented in English as required by industry regulatory agencies.
Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences
-
Clinical Investigator
4 days ago
Montreal, Quebec, Canada Altasciences Full time $120,000 - $180,000 per yearYour New CompanyAt Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of...
-
Senior Clinical Investigator
3 weeks ago
Montreal, Canada Altasciences Co. Full timeA leading clinical research organization is seeking a Clinical Investigator (MD) in Montreal. You will oversee clinical trial activities, ensure compliance with Good Clinical Practice, and maintain subject safety. The ideal candidate will have an active medical license in Quebec, strong communication skills in French and English, and experience in clinical...
-
Licensed Practical Nurse
4 days ago
Site Montreal - Beaumont, Canada Altasciences Full time $60,000 - $90,000 per yearYour New CompanyAt Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of...
-
Study Manager
2 weeks ago
Site Montreal - Beaumont, Canada Altasciences Full time $80,000 - $120,000 per yearYour New CompanyAt Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of...
-
Remote Director, Clinical Quality Events
4 weeks ago
Toronto, Montreal, Calgary, Vancouver, Edmonton, Old Toronto, Ottawa, Mississauga, Quebec, Winnipeg, Halifax, Saskatoon, Burnaby, Hamilton, Victoria, Surrey, Halton Hills, London, Regina, Markham, Brampton, Vaughan, Kelowna, Laval, Southwestern Ontario, R, Canada ICON Strategic Solutions Full timeA leading strategic solutions firm is seeking a Senior Quality Events/Issues Lead to manage quality investigations and ensure GCP compliance in clinical research. The ideal candidate will have extensive experience in pharmaceutical quality and regulatory requirements, with solid communication and project management skills. This full-time position is critical...
-
Clinical Research Coordinator
4 days ago
Montreal, Quebec, Canada CUSM Full time $45,000 - $60,000 per yearDo you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal At the Research Institute of the McGill University Health Centre (RI-MUHC), you can be part of an organization focused on scientific discovery and innovation in patient-centered medicine. Join us today and...
-
Clinical Research Specialist
2 weeks ago
Montreal, Quebec, Canada Lallemand Full time $60,000 - $100,000 per yearMain FunctionsUnder the direct supervision of the Clinical Operations Director, the Clinical Research Specialist (CRS) will be responsible for the oversight of evidence-based clinical trials of Lallemand probiotic strains and yeast formulations. The CRS will also be responsible for managing clinical trial documentation and implementing applicable regulatory...
-
FSP Clinical Research Associate
3 days ago
Montreal, Quebec, Canada myGwork - LGBTQ+ Business Community Full time US$83,000 - US$125,000 per yearThis job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific, you'll discover meaningful work that makes a positive...
-
Clinical Study Manager
4 weeks ago
Montreal, Canada AbCellera Full timeClinical Study Manager Join to apply for the Clinical Study Manager role at AbCellera. AbCellera’s platform integrates biology, computation, and engineering to develop impactful antibody‑based medicines. We’re scientists, engineers, and business professionals working together to turn scientific insights into breakthrough medicines. We pursue truth and...
-
Clinical Research Coordinator
4 weeks ago
Montreal, Canada RI-MUHC | Research Institute of the MUHC | #rimuhc Full timeClinical Research Coordinator (Research Institute) Do you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal! At the Research Institute of the McGill University Health Centre (RI‑MUHC), you can be part of an organization focused on scientific discovery and...