Clinical Research Study Assistant

2 days ago

Toronto, Canada Humber River Health Full time

Position Profile:
**Humber River Health. Lighting New Ways In Healthcare.**

Since opening our doors in 2015 as North America’s first fully digital hospital, we remain unwavering in our belief that we can change the hospital where we work, the community where we live, and the world of healthcare beyond our borders. Serving a community of 850,000 residents in North West Toronto, Equity Inclusivity and active participation in the North West Toronto Ontario Health Team are key initiatives important to our Team. At Humber River Health, we use a custom combination of technology and clinical expertise to rebuild elements of care. We make technology work for staff and physicians; giving them more time to spend with patients, to eliminate inefficiencies, and to reduce the chance of errors. Humber River Health is formally affiliated with both the University of Toronto and Queen’s University and committed to becoming a community academic hospital. Clinical Excellence, Optimizing Care through Technology and Community Connection frame our Research Strategy.

At Humber River Health, we’re not hoping for a renaissance, we are making it happen. As part of our dynamic team, you can lead the way, as we continue our journey towards high reliability care

**Clinical Research Study Assistant**

**Reporting Relationship**:Manager, Research

**Location**:Humber River Health - Wilson Site

**Employee Group**:Non Union

**Duration**: Temporary Full Time (approximately 12 months)

**Responsibilities**:

- Assist in interactions with study participants; e.g., scheduling appointments, administer telephone interviews to collect basic study participant data using established criteria and other administrative functions
- Prepares, receives, sorts and processes clinical research samples/specimens following established procedures and guidelines and in compliance with applicable regulations
- Performs limited testing within scope of qualifications and with appropriate training (e.g. medication history) for research purposes
- Provides assistance to the research team in planning and preparing for research activities as per protocol
- Prepares documents, equipment, supplies, etc. in compliance with the protocol.
- May assist with the collection of medical documents as per approved study protocol and authorized access
- Participates in study team meetings
- Under supervision may collect information about adverse events (AEs), identified in the protocol or investigator brochure.
- May assist in the preparation of submissions to the Research Ethics Board (REB).
- Executes study-related administrative tasks, such as collection and maintenance of regulatory documents, ethics submissions, the maintenance & modification of electronic & paper information filing/retrieval methods, systems and/or formats, performing data abstraction from health records or other sources, as per approved study protocol and authorized access and follow SOPs for quality assurance and to assist in documenting and maintaining documentation
- May assist with simple literature searchers under close supervision.
- As directed, assist in preparing studies for closeout (e.g., packing files, documenting files for storage, shipping extra supplies back to sponsor).
- Communicates with other research personnel as required for study implementation and routine problem resolution.

**Qualifications**:

- Undergraduate Degree in Health or Science-related discipline required
- Recent 1-2 years clinical and/or professional experience in Research
- Experience in MS Office (e.g. Outlook, Word, Excel, PowerPoint, Access, etc.)
- Fundamental knowledge of research principles and practice, regulations and guidelines, such as ICH/GCP guidelines, Tri-Council Policy, Declaration of Helsinki and FDA CFR and Health Canada TPD, as required
- Knowledge of IATA shipping regulations and basic laboratory procedures, as required

**Why choose Humber River Health?**

At Humber River Health, our staff, physicians, and volunteers are lighting new ways in healthcare. We are proud to be recognized as a part of Greater Toronto’s Top Employers by Mediacorp Canada Inc. We support employees by providing evidence-based leadership and cultivating a culture that consistently wows as a Huron Consulting hospital. We are a member of the Toronto Academic Health Science Network (TAHSN) and are deeply involved in research and academic collaboration. We are dedicated to high-quality patient care and demonstrate our values of compassion, professionalism, and respect.

Attracting and retaining a workforce that represents the diverse communities surrounding Humber River Health, is a priority. We encourage applicants from all equity-deserving groups, including but not limited to, individuals who identity as Indigenous, racialized, seniors, persons living with disabilities, women, and those who identify as 2SLGBTQ.

Applicants will not be discriminated against on the basis of race, creed, sex, sexual orientation, gender

  • Clinical Research Coordinator

    6 months ago

    Toronto, Canada Clinical Research Full time

    Responsibilities: - Coordinate and oversee clinical research studies from start to finish - Collect and record data accurately and efficiently - Analyze research data and prepare reports for review - Ensure compliance with study protocols, regulations, and ethical guidelines - Collaborate with healthcare professionals, researchers, and study participants -...

  • Clinic Study Assistant

    2 months ago

    Toronto, Canada Pharma Medica Research Inc. Full time

    Pharma Medica Research Inc. is a full-service contract research organization in need of a Clinic Study Assistant to join our team in Scarborough! The Clinic Study Assistant assists with general clinical duties as required by Pharma Medica Research Inc. (PMRI). This position reports to the Manager, Group Leader/or designate. Duties and...

  • Clinical Research Assistant

    6 months ago

    Toronto, Canada North York Research Inc. Full time

    North York Research Inc. is the Clinical Trial Division of North York Dermatology Clinic. North York Research Inc. is seeking an enthusiastic individual to join our team as a Clinical Research Assistant. This position has the potential of developing into a Clinical Research Coordinator role. **Responsibilities**: - Assist Clinical Research Coordinators in...

  • Clinical Research Document Specialist

    3 weeks ago

    Toronto, Ontario, Canada Everest Clinical Research Services Inc Full time

    Job DescriptionJob Title: Clinical Research Document SpecialistCompany: Everest Clinical Research Services IncLocation: Remote or Toronto/Markham, Ontario, CanadaJob Type: Full-timeAbout Us:Everest Clinical Research Services Inc is a leading contract research organization (CRO) providing clinical research services to pharmaceutical, biotechnology, and...

  • Clinical Research Budget Analyst

    3 weeks ago

    Toronto, Ontario, Canada Everest Clinical Research Services Inc Full time

    Clinical Research Budget Analyst Position at Everest Clinical Research Services IncEverest Clinical Research Services Inc is a leading contract research organization (CRO) providing comprehensive clinical research services to the pharmaceutical, biotechnology, and medical device industries. We are seeking an experienced Clinical Research Budget Analyst to...

  • Research Assistant

    6 months ago

    Toronto, Canada Centricity Research Full time

    POSITION FUNCTION The Research Assistant (RA) performs a variety of administrative and clinical activities to assist the Investigators and CRCs in conducting clinical studies. The RA will have a strong understanding of study protocols and will support study activities completely and accurately. ESSENTIAL FUNCTIONS Protocol and Safety: - Ensure the safety...

  • Clinical Research Associate

    2 weeks ago

    Toronto, Ontario, Canada Everest Clinical Research Services Inc Full time

    Everest Clinical Research Services Inc. is a renowned full-service contract research organization (CRO) providing expertise-based clinical research services to pharmaceutical, biotechnology, and medical device industries worldwide.We serve top companies and collaborate with cutting-edge drugs, biologics, and medical devices in development.The company has...

  • Clinical Research Coordinator

    5 months ago

    Toronto, Canada Headlands Research Full time

    Overview: - Toronto Memory Program, a Headlands Research site, is Canada’s largest and most experienced site for drug treatment trials in Alzheimer’s disease and related conditions. Founded in 1996, we have made significant contributions to over 100 drug treatment studies in Alzheimer’s disease. Our Medical Director, Dr. Sharon Cohen, a...

  • Clinical Research Coordinator

    5 months ago

    Toronto, Canada Headlands Research Full time

    Overview: **The Role** Toronto Memory Program is looking for a Clinical Research Coordinator to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines. **This Clinical Research Coordinator role will be based in...

  • Clinical Research Coordinator

    1 month ago

    Toronto, Ontario, Canada Pharma Medica Research Inc. Full time

    Job Title: Clinical Research CoordinatorPharma Medica Research Inc. is a leading contract research organization seeking a Clinical Research Coordinator to support our clinical studies in Scarborough. As a key member of our team, you will assist with the coordination of clinical duties, ensuring the smooth execution of studies.Key Responsibilities:Coordinate...

  • Clinical Research Study Coordinator

    5 months ago

    Toronto, Canada SickKids Full time

    **About SickKids**: Dedicated exclusively to children and their families, The Hospital for Sick Children (SickKids) is one of the largest and most respected paediatric healthcare centres in the world. As innovators in child health, we lead and partner to improve the health of children through the integration of healthcare, leading-edge research and...

  • Clinical Research Recruitment Assistant

    6 months ago

    Toronto, Canada Headlands Research Full time

    **Overview**: - Toronto Memory Program, a Headlands Research site, is Canada’s largest and most experienced site for drug treatment trials in Alzheimer’s disease and related conditions. Founded in 1996, we have made significant contributions to over 100 drug treatment studies in Alzheimer’s disease. Our Medical Director, Dr. Sharon Cohen, a...

  • Clinical Research Recruitment Assistant

    6 months ago

    Toronto, Canada Headlands Research Full time

    Overview: - Toronto Memory Program, a Headlands Research site, is Canada’s largest and most experienced site for drug treatment trials in Alzheimer’s disease and related conditions. Founded in 1996, we have made significant contributions to over 100 drug treatment studies in Alzheimer’s disease. Our Medical Director, Dr. Sharon Cohen, a...

  • Clinical Research Study Assistant

    6 months ago

    Toronto, Canada University Health Network Full time

    Company Description The University Health Network, where “above all else the needs of patients come first”, encompasses Toronto General Hospital, Toronto Western Hospital, Princess Margaret Cancer Centre, Toronto Rehabilitation Institute and the Michener Institute of Education. The breadth of research, the complexity of the cases treated, and the...

  • Senior Clinical Research Budget Manager

    2 weeks ago

    Toronto, Ontario, Canada Everest Clinical Research Services Inc Full time

    Job TitleSenior Clinical Research Budget ManagerCompany OverviewEverest Clinical Research Services Inc is a leading contract research organization (CRO) providing clinical research services to the pharmaceutical, biotechnology, and medical device industries.About the JobWe are seeking a highly skilled Senior Clinical Research Budget Manager to join our team...

  • Senior Biostatistician

    3 weeks ago

    Toronto, Ontario, Canada Everest Clinical Research Services Inc Full time

    We are seeking a highly skilled Senior Biostatistician to join our team at Everest Clinical Research Services Inc. The ideal candidate will have a Ph.D. degree in statistical science or a related field with at least 5 years of relevant experience.Main Responsibilities:• Develop and implement statistical methodologies for clinical trial programs.• Lead...

  • Biostatistics Leadership Position in Clinical Research

    2 weeks ago

    Toronto, Ontario, Canada Everest Clinical Research Services Inc Full time

    About Everest Clinical Research Services Inc.Everest Clinical Research Services Inc. is a reputable full-service contract research organization (CRO) providing comprehensive clinical research services to pharmaceutical, biotechnology, and medical device industries worldwide. Our team collaborates with top companies to advance innovative drugs, biologics, and...

  • Clinical Study Assistant Ii Ahrc Obs Research Unit

    7 months ago

    Toronto, Canada Unity Health Toronto Full time

    The Applied Health Research Centre (AHRC) at St. Michael¿s Hospital is currently seeking a Clinical Study Assistant II. The Clinical Study Assistant II will report directly to the Manager, Observational Epidemiology and Qualitative Research Unit (OEQRU), and will support research studies managed by the OEQRU. The primary role of the Clinical Study...

  • Clinical Research Proposals Strategist

    2 weeks ago

    Toronto, Ontario, Canada Everest Clinical Research Services Inc Full time

    Everest Clinical Research Services Inc: Contracts and Proposals ManagerWe are seeking a skilled Clinical Research Proposals Strategist to join our team at Everest Clinical Research Services Inc. in Bridgewater, New Jersey, USA.

  • Clinical Research Assistant

    6 months ago

    Toronto, Canada FACET Dermatology Full time

    FACET Dermatology is looking for a Clinical Research Assistant to work closely with the clinical research coordinators to assist in study operations. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines. **Responsibilities** - Work collaboratively...