Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science from an accredited university; * At least 2 years as a Clinical Research Associate or Clinical ...
Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science from an accredited university; * At least 2 years as a Clinical Research Associate or Clinical ...
Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science from an accredited university; * At least 2 years as a Clinical Research Associate or Clinical ...
Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science from an accredited university; * At least 2 years as a Clinical Research Associate or Clinical ...
Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science from an accredited university; * At least 2 years as a Clinical Research Associate or Clinical ...
Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science from an accredited university; * At least 2 years as a Clinical Research Associate or Clinical ...
Drive operational "hygiene" by developing and implementing evidence-based clinical protocols, conducting chart audits, overseeing clinical reviews, managing patient escalations, and formalizing ...
Drive operational "hygiene" by developing and implementing evidence-based clinical protocols, conducting chart audits, overseeing clinical reviews, managing patient escalations, and formalizing ...
Drive operational "hygiene" by developing and implementing evidence-based clinical protocols, conducting chart audits, overseeing clinical reviews, managing patient escalations, and formalizing ...
Drive operational "hygiene" by developing and implementing evidence-based clinical protocols, conducting chart audits, overseeing clinical reviews, managing patient escalations, and formalizing ...
Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating ... Review progress of projects and initiate appropriate actions to achieve target objectives.
Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating ... Review progress of projects and initiate appropriate actions to achieve target objectives.
Perform clinical trial activities including but not limited to safety assessments and blood ... Annual Performance Reviews. #LI-JG1 MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH ...
Perform clinical trial activities including but not limited to safety assessments and blood ... Annual Performance Reviews. #LI-JG1 MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH ...
Associate Director, Regulatory Affairs & Submissions - Nonclinical Development
Montreal, QC · On-site
Lead the preparation and critical review of nonclinical sections of regulatory submissions (IND, CTA, NDA/BLA), ensuring scientific rigor and regulatory compliance. * Conduct gap analyses of non ...
Associate Director, Regulatory Affairs & Submissions - Nonclinical Development
Montreal, QC · On-site
Lead the preparation and critical review of nonclinical sections of regulatory submissions (IND, CTA, NDA/BLA), ensuring scientific rigor and regulatory compliance. * Conduct gap analyses of non ...
Lead the preparation and critical review of nonclinical sections of regulatory submissions (IND, CTA, NDA/BLA), ensuring scientific rigor and regulatory compliance. * Conduct gap analyses of non ...
Lead the preparation and critical review of nonclinical sections of regulatory submissions (IND, CTA, NDA/BLA), ensuring scientific rigor and regulatory compliance. * Conduct gap analyses of non ...
CRA 1/2 & Sr. CRAs - Oncology & General Medicine, French Speaking Desired- Canada
Montreal, QC · Remote
... review guidelines on Fortrea or client data management systems as assigned by management * Assist with training of new employees, eg. co-monitoring * Coordinate designated clinical projects as a ...
CRA 1/2 & Sr. CRAs - Oncology & General Medicine, French Speaking Desired- Canada
Montreal, QC · Remote
... review guidelines on Fortrea or client data management systems as assigned by management * Assist with training of new employees, eg. co-monitoring * Coordinate designated clinical projects as a ...
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 ... Develop and review nursing care plans that are individualized to each patient; * Conducts patient ...
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 ... Develop and review nursing care plans that are individualized to each patient; * Conducts patient ...
About the Role We are seeking a Fullstack Developer (Python) to join our Clinical team. The ... Participate in and contribute to code reviews to improve your skills in the areas of component ...
About the Role We are seeking a Fullstack Developer (Python) to join our Clinical team. The ... Participate in and contribute to code reviews to improve your skills in the areas of component ...
Participate in the development or adaptation of clinical tools and quality-of-care assessment processes. * Coordinate team activities and serve as a resource person for the nursing and ...
Participate in the development or adaptation of clinical tools and quality-of-care assessment processes. * Coordinate team activities and serve as a resource person for the nursing and ...
CA$75K/yr
Review and draft study plans/protocols for PK and TK studies, including amendments and preparation ... Charles River also provides a suite of products and services to support our clients' clinical ...
CA$75K/yr
Review and draft study plans/protocols for PK and TK studies, including amendments and preparation ... Charles River also provides a suite of products and services to support our clients' clinical ...
... review and approval Your profile: * A holder of a Bachelor's degree in a scientific or healthcare-related field (highly preferred). * An experienced Clinical Research Associate with a minimum of 2 ...
... review and approval Your profile: * A holder of a Bachelor's degree in a scientific or healthcare-related field (highly preferred). * An experienced Clinical Research Associate with a minimum of 2 ...
Supportappropriate interpretationand communication of clinical trialdata. * Review and approve submission level safety narrativeplan. * Supports product label development andmaintenance.
Supportappropriate interpretationand communication of clinical trialdata. * Review and approve submission level safety narrativeplan. * Supports product label development andmaintenance.
Supportappropriate interpretationand communication of clinical trialdata. * Review and approve submission level safety narrativeplan. * Supports product label development andmaintenance.
Supportappropriate interpretationand communication of clinical trialdata. * Review and approve submission level safety narrativeplan. * Supports product label development andmaintenance.
CRA I / CRA II - Sponsor Dedicated - Bilingual French and English (Home-based - Montreal, Quebec)
Montreal, QC · On-site
Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required ...
CRA I / CRA II - Sponsor Dedicated - Bilingual French and English (Home-based - Montreal, Quebec)
Montreal, QC · On-site
Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required ...
CRA II / Sr CRA - Sponsor Dedicated | Oncology | Bilingual in French and English (Home-Based - Mo...
Montreal, QC · On-site
Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required ...
CRA II / Sr CRA - Sponsor Dedicated | Oncology | Bilingual in French and English (Home-Based - Mo...
Montreal, QC · On-site
Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required ...
Review and understand all assigned actively enrolling studies. * Answer in-coming calls and internet applications/web-submission forms from clinical trial participants. * Contact past/potential ...
Review and understand all assigned actively enrolling studies. * Answer in-coming calls and internet applications/web-submission forms from clinical trial participants. * Contact past/potential ...
Clinical Reviewer information
What is a clinical reviewer?
What does a clinical reviewer do?
A clinical reviewer monitors healthcare documents to ensure compliance before submitting to insurance companies. You handle the daily responsibilities of checking medical records for appropriate criteria and providing the proper documentation. You collaborate with providers to ensure all information is accurate. Your duties are also to review requests for services, research and gather further information when necessary, perform an information audit, and evaluate procedures for approval. You also record, analyze, and report data elements that could help improve the quality of care of a patient.
What skills are required for a clinical reviewer?
What are some common challenges clinical reviewers face when evaluating medical records, and how can they be addressed?
What is the difference between Clinical Reviewer vs Medical Reviewer?
| Aspect | Clinical Reviewer | Medical Reviewer |
|---|---|---|
| Required Credentials | RN, LPN, or other healthcare licenses; sometimes certifications in case management or clinical review | MD or DO; medical license; often board-certified in a specialty |
| Work Environment | Insurance companies, healthcare organizations, or government agencies; reviewing medical records and claims | Hospitals, clinics, insurance companies; evaluating medical records and providing expert opinions |
| Employer & Industry Usage | Primarily in insurance and healthcare administration | Primarily in insurance, healthcare, and legal settings |
Both Clinical Reviewers and Medical Reviewers assess medical information, but Clinical Reviewers typically hold nursing or allied health credentials and focus on case management and claims review. Medical Reviewers are licensed physicians who provide expert medical opinions. The roles often overlap in insurance and healthcare industries, but their credentials and scope of practice differ.
What are popular job titles related to Clinical Reviewer jobs in Quebec?
For Clinical Reviewer jobs in Quebec, the most frequently searched job titles are:
What job categories do people searching Clinical Reviewer jobs in Quebec look for?
The top searched job categories for Clinical Reviewer jobs in Quebec are:

Full-time
Medical, Retirement, PTO
Re-posted 17 days ago
Medpace rating
8.6
Based on 12 frontline employees who took The Breakroom Quiz
13th of 73 rated research
Job description
Medpace is growing quickly and we are seeking a Clinical Research Associate to join our team in Montreal Canada. We are an innovative, scientifically oriented mid-sized CRO that is focused on full-service project work.
This is a home-based position in Montreal Canada.
Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence and receive customized, expedited training, and efficient onboarding to familiarize experienced CRAs with Medpace systems.
WE OFFER THE FOLLOWING
- Competitive bonus plans including Resourcing Bonus (following training completion and successful assignment to studies) and Yearly Travel Incentives
- Voluntary retirement scheme
- Home office furniture allowance, mobile phone and hotspot for internet access anywhere
- In-house travel agents, reimbursement for airline club and TSA pre-check
- Customized PACE training program based on your experience and therapeutic background and interest
- User friendly CTMS with electronic submission and approval of monitoring visit reports
- Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts
- National assignments with average of 2 protocols
- In-house administrative support for all levels of CRAs
- Opportunities to work with international team of CRAs
- Low turnover rates for CRAs
- No metric for minimum required days on site per month
- Flexible work hours across days within a week
- Opportunity for CRA leadership positions - Lead CRA, CRA Manager
- Many additional perks unmatched by other CROs!
- Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Medpace/Sponsor SOPs and GCP;
- Maintain ongoing site correspondence and site files;
- Complete visit reports and maintaining study-related databases;
- Oversight and interaction with clinical research sites; and
- Review of patient charts and clinical research data.
- Bachelor's degree in science from an accredited university;
- At least 2 years as a Clinical Research Associate or Clinical Research Coordinator;
- Bilingual in English and French;
- Thorough knowledge of the methodology related to the conduct and monitoring of clinical trials per ICH E-6 guidelines and per Part-C, Division 5 of the Health Canada Food and Drug regulations;
- Excellent interpersonal, written and verbal communication skills in English and French;
- Strong attention to detail and organization skills;
- Highly motivated, independent, flexible;
- Ability to travel between 60-80%;
- Ability to prioritize workload to meet timelines across multiple studies; and
- Proficient in Microsoft Office.
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
-
- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
-
- Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
- Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
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- Office based environment with on-site mentors
- Defined career paths with clear advancement opportunities
- Industry renowned onboarding and training programs designed to accelerate professional development
- Ongoing training and continuous learning opportunities throughout your career
- An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
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- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events
Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
Employment Type: OTHERAbout Medpace
Sourced by ZipRecruiter
Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.
Industry
Medical equipment and supplies manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Cincinnati, OH, US
Year founded
1992