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Equity research Jobs in Dollard-Des Ormeaux, QC

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Equity research • dollard des ormeaux qc

Last updated: 1 day ago
  • Promoted
Clinical Research Associate

Clinical Research Associate

Headssaint-esprit, qc, Canada
Full-time
Heads, a global CRO, is seeking a Clinical Research Associate (CRA) based in Canada for its growing international hematology / oncology Clinical Trials program. The CRA is responsible for ensuring tha...Show moreLast updated: 1 day ago
  • Promoted
Account Executive

Account Executive

asobbisaint-esprit, qc, Canada
CA$350,000.00 yearly
Full-time
Enterprise Account Executive – up to $350,000 OTE Uncapped + Equity.Currently seeking a highly experienced, driven, determined and tenacious person for a rapidly expanding AI company providing cutt...Show moreLast updated: 2 days ago
  • Promoted
Clinical Research Associate / Project Supervisor (French Speaker)

Clinical Research Associate / Project Supervisor (French Speaker)

Tigermedlaval, qc, Canada
Full-time
This Positions is a mixed Role of CRA and Project Supervisor.This position is responsible for project management and study site management from site selection to initiation until monitoring and clo...Show moreLast updated: 2 days ago
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Junior Research Analyst

Junior Research Analyst

avuasaint-esprit, qc, Canada
Full-time
You will be responsible for conducting in-depth analysis, monitoring industry trends, and providing valuable insights to support strategic decision-making within the energy sector.The ideal candida...Show moreLast updated: 1 day ago
Research Advisor

Research Advisor

Cuso InternationalLaval, QC, CA
This Volunteer Placement is Located in : .Please submit a Spanish Resume and Statement of Interest.Eligibility : Open to Canadian Citizens and Permanent Residents of Canada only.This is your opportuni...Show moreLast updated: 30+ days ago
  • Promoted
Research & Development Technologist

Research & Development Technologist

Yoplait Liberté CanadaGreater Montreal Metropolitan Area, Canada
Full-time
The Dairy Research and Development Technologist, specializing in yogurt manufacturing, supports new product development activities, pilot tests, and production trials. They work under the supervisio...Show moreLast updated: 1 day ago
Research Assistant, R&D

Research Assistant, R&D

CIRION BioPharma ResearchLaval, Canada
CA$47,320.00–CA$87,887.80 yearly
Description Research Assistant, R&D (RH2024-003)Location : Laval, Canada CIRION BioPharma Research is looking for a Research Assistant. Under the supervision of the Director, Research and Development...Show moreLast updated: 30+ days ago
Remote Equity Trader Job in Salluit, QC | Part Time

Remote Equity Trader Job in Salluit, QC | Part Time

Maverick TradingSalluit, Nord-du-Québec, QC J0M, Canada
CA$25,000.00 yearly
Remote
Part-time
Remote Equity Trader Job at Maverick Trading.Maverick Trading, a 26-year old proprietary trading firm is looking to hire experienced and entry-level equity and equity and option traders.We are a gl...Show moreLast updated: 30+ days ago
  • Promoted
Laboratory Coordinator / Research Assistant - Human Performance (CANSOFCOM)

Laboratory Coordinator / Research Assistant - Human Performance (CANSOFCOM)

Canadian Forces Morale and Welfare Services - CFMWSMontréal North, CA
Full-time
CFMWS - WHERE PURPOSE MEETS PASSION At Canadian Forces Morale and Welfare Services (CFMWS), we’re more than just a workplace. we’re a proud community dedicated to supporting Canadian Armed Forces m...Show moreLast updated: 4 days ago
(Anticipatory) Senior Investigator-Operations (Air) - Restricted to Employment Equity Groups

(Anticipatory) Senior Investigator-Operations (Air) - Restricted to Employment Equity Groups

Treasury Board of Canada SecretariatDorval, Québec
CA$113,880.00–CA$133,570.00 yearly
Anticipatory) Senior Investigator-Operations (Air) - Restricted to Employment Equity Groups.TSB-AIR-INV-EA-006 Transportation Safety Board of Canada. Calgary (Alberta), Edmonton (Alberta), Richmond ...Show moreLast updated: 30+ days ago
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Analyst M&A, Private Equity Roll-up

Analyst M&A, Private Equity Roll-up

AYCE Capitallaval, qc, Canada
Full-time
AYCE Capital’s Managed Service Provider (MSP) Platform is one of Canada’s fastest growing MSP players.Our exciting growth trajectory is due to our fast-paced and accelerating M&A team.AYCE Capital’...Show moreLast updated: 2 days ago
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Associate

Associate

Peloton Search PartnersGreater Montreal Metropolitan Area, Canada
Full-time
Introduction : Peloton Search Partners is a specialized recruitment firm with a focus on finance and investment.Our clients are well-known and active in private equity (and portfolio companies), priv...Show moreLast updated: 24 days ago
Remote Data Research Intern

Remote Data Research Intern

FocusGroupPanelSaint-Louis-de-Gonzague, Quebec, Canada
Remote
Full-time +1
Remote Work From Home Data Entry Clerk for Entry Level Position.Work at home position for job seekers from virtually any work background who are interested in part-time, side gigs, micro jobs, wo...Show moreLast updated: 6 days ago
  • Promoted
E-commerce coordinator

E-commerce coordinator

Randstad CanadaLaval, Quebec, CA
Temporary
Quick Apply
Are you a person who likes to coordinate e-commerce tasks? Do you have the fiber of customer service in addition to being bilingual and super comfortable with computers? If you answered yes to thes...Show moreLast updated: 27 days ago
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Head of Finance (Research / Contract)

Head of Finance (Research / Contract)

Ripplingsaint-esprit, qc, Canada
CA$200.00 daily
Full-time
This is an open freelance role to share your feedback.We are looking for feedback from Finance Leaders on our product as we expand in Canada. This is a compensated research hourly research role in e...Show moreLast updated: 2 days ago
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Ramp Agent

Ramp Agent

Transat ATDorval, Quebec, Canada
The incumbents will be responsible for the processing of luggage both at the departures and arrivals levels.The ramp agent prepares loads and unloads luggage from the aircrafts.The ramp agent marsh...Show moreLast updated: 30+ days ago
  • Promoted
Coordinator, Data & Impact

Coordinator, Data & Impact

Let's Talk Science | Parlons scienceslaval, qc, Canada
Full-time +1
Do you want to help us execute on our data strategy to inform decision-making and use results to tell our story?.Do you want to make a difference to children and youth across Canada?.We invite you ...Show moreLast updated: 2 days ago
Oncology Clinical Research Associate - Canada -

Oncology Clinical Research Associate - Canada -

ScimegaLaval, Quebec
CA$46,147.00 yearly
Under the direction of the Director, Clinical and Scientific Affairs, the CTL is responsible for execution of clinical trials, from the site selection, start-up and enrollment phases up to the stud...Show moreLast updated: 30+ days ago
Senior Manager, Rewards, Equity & Incentives Tax Advisory

Senior Manager, Rewards, Equity & Incentives Tax Advisory

DeloitteLaval, QC
CA$116,000.00–CA$215,000.00 yearly
Toronto, ON; Brossard, QC; Burlington, ON; Calgary, AB; Edmonton, AB; Fredericton, NB; Halifax, NS; Kitchener, ON; Laval, QC. Moncton, NB; Montreal, QC; Ottawa, ON; Quebec City, QC; Regina, SK; Sai...Show moreLast updated: 30+ days ago
  • Promoted
Manager of Market Research and Commercial Insights

Manager of Market Research and Commercial Insights

Telnalaval, qc, Canada
Full-time
Telna is seeking an experienced and strategic Director of Market Research and Commercial Insights to lead our market research initiatives and commercial strategy development.In this role, you will ...Show moreLast updated: 2 days ago
Clinical Research Associate

Clinical Research Associate

Headssaint-esprit, qc, Canada
1 day ago
Job type
  • Full-time
Job description

Heads, a global CRO, is seeking a Clinical Research Associate (CRA) based in Canada for its growing international hematology / oncology Clinical Trials program.

This is a full-time job.

Job overview :

The CRA is responsible for ensuring that the conduct of a clinical trial at selected Investigational Sites is according to the currently approved protocol / amendments, ICH GCP guidelines, the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations.

He / she is the primary responsible person for communication on operational study related activities between the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships.

The most important responsibility is to ensure that the subjects’ rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents.

Main responsibilities :

  • Acknowledges, follows& ensures compliance with the Company’s Quality and Information Security Management Systems, ICH GCP guidelines, applicable local and international legislation, including data protection legislation, as well as any amendments or updates the above
  • In case of deviation from the approved protocol, ICH GCP guidelines and / or applicable legislation during the study conduct, the CRA is responsible for reporting it to the Line Manager and other applicable roles according to SOPs
  • Conducts pre-study visits at potential investigational sites, to perform the study related feasibility and / or selection activities and evaluate their resources and facilities
  • Collaborates with the Regulatory Affairs Department and concerned Clinical Operations staff for clinical submissions and contracts respectively for :
  • Managing Hospital IEC study submissions and approvals with follow through to ensure successful outcome
  • Preparation of study contracts & relevant files to be submitted for the study financial management acceptance, as required by the applicable local legislation
  • Fully explains the purposes, set-up, and procedures of the clinical trial to the Investigators and is responsible for training and assisting them in the conduct of clinical trials
  • Prepares and updates the Clinical Trial Files throughout the study and ensures the proper collection of essential documents and other study-related documents during the trial
  • Ensures that the Sites are supplied with adequate study medication, verifies that drug accountability is performed correctly and ensures the drug’s safe shipment, storage, dispensing, return and destruction, as applicable
  • The CRA is responsible for adequate monitoring of the clinical trial conduct at the Investigational Sites (e.g., performs monitoring visits at the Sites) during which he / she :
  • Ensures Investigators’ knowledge and compliance with the clinical protocol and ICH GCP guidelines
  • Verifies that Investigators’ qualifications and resources remain adequate throughout the trial period
  • Reviews and verifies the data reported in the eCRF against source data, according to the monitoring plan which determines the depth and extend of source data verification
  • Ensures that written informed consent has been obtained from all subjects prior to any study related screening activity or requirement
  • Fully verifies subject consent procedures against ICH GCP guidelines and legislation
  • Checks and discusses recruitment and timelines with the Investigators
  • Checks the storage and adequacy of clinical trial supplies
  • Maintains and updates the Investigator’s Files as required to confirm completeness
  • Co-ordinates the proper reporting of Safety Information to the Sponsor according to the Safety Reporting Plan, where applicable. CRA is also responsible for making sure that the Investigators are adequately trained in identifying and reporting AEs / SAEs
  • Checks that all submissions, reports, notifications and applications to the IEC / IRB or Regulatory Authorities have been made by the Investigator in a timely manner
  • Performs drug accountability and ensures the proper dispensing of study drug to the patient
  • Prepares reports to document all discussions, measures and actions made during a monitoring visit, telephone contact or remote monitoring. The CRA also sends summary of these reports to the Investigators
  • Participates in study specific conference calls and meetings to review progress of ongoing clinical trials; provides feedback to the CRA Manager
  • In case of an audit or regulatory inspection, the CRA is responsible for informing and preparing the Site and facilitating the procedure. The CRA works with the appropriate study team members and Quality (QA) in order the corrective actions are in place and performed as soon as possible
  • Collaborates with the CRA Manager and Clinical Operations Manager to develop feasibility evaluation questionnaires, contact the Investigators to collect feasibility-related information, perform site screening and selection
  • Supports financial issues of the study, including Investigators’ payments
  • Manages timely subject enrolment and quality data collection
  • Ensures that procedures are in place for appropriate optimization of patients into the study : evaluates patients’ recruitment and determines if it is according to the operational plan & patients’ target
  • Closes down study sites on completion of the trial
  • Participates in departmental planning sessions, and SOP development, if required
  • Provides coaching, mentoring and management to the newly appointed and / or inexperienced CRAs to ensure that their role and contribution is optimized

Job Requirements :

  • Bachelor’s and / or master’s degree (preferably in Health Sciences)
  • Previous Work Experience desirable :
  • 6-12 months’ work experience as a CRA
  • Excellent command of English and French both oral and written
  • Attendance of an ICH GCP training course (desirable)
  • Good computer skills
  • Good general communication skills
  • Good organizational skills
  • Ability to work independently and be a good team player at the same time
  • Ability to communicate diplomatically, but also effectively with study Site personnel
  • Ability to deal adequately with stressful situations, flexible timelines and work pressure
  • Ability to maintain complete overview and deal with several issues at the same time
  • Ability to work according to specific SOPs, guidelines, regulations & ethical principles in the daily practice
  • Ability for frequent international and local travelling, including evenings and overnight stays
  • Join us to be part of a multidisciplinary team of highly skilled scientists and healthcare professionals in the forefront of Clinical Research within a friendly work environment.

    Competitive remuneration package comes on top.

    In Heads we consider Data Protection an integral part of our operational business principles and are committed to respecting your privacy. For information on how we process your personal data please visit our Privacy Notice to Candidates :