Clinical Research and Trials Coordinator – BC Cancer Vancouver – Provincial Health Services Authority – Vancouver, BC

Company: Provincial Health Services Authority

Location: Vancouver, BC

Job description: Clinical Research and Trials Coordinator BC Cancer Vancouver, BC For a specific trial or project, the Clinical… Research and Trials Coordinator (CRTC) receives direction from the Qualified Investigator/Principal Investigator, Manager…
The Clinical Research and Trials Coordinator (CRTC) at BC Cancer in Vancouver, BC, works under the direction of the Qualified Investigator/Principal Investigator and the Manager. The CRTC is responsible for coordinating specific trials or projects, ensuring compliance with protocols, managing data collection, and supporting the research team’s goals. Duties include patient enrollment, maintaining records, and facilitating communication among team members and stakeholders.

The job description for the Clinical Research and Trials Coordinator position at BC Cancer Vancouver, as listed on the Provincial Health Services Authority website, includes the following details:

Position Title: Clinical Research and Trials Coordinator

Location: Vancouver, BC

Salary: $40.94–$51.10 per hour

Employment Type: Permanent, Full-time

Job Overview:
The Clinical Research and Trials Coordinator (CRTC) is responsible for coordinating clinical trial activities to ensure that the objectives of the clinical trial are met. This includes organizing special projects related to the clinical trial, drafting grant applications, maintaining research activities, determining data requirements, and coordinating data capture activities. The CRTC also assists with preparing documentation required for ethics review and organizes relevant material required for internal and external audits and inspections.

Key Responsibilities:

  • Coordinate, organize, and perform special work assignments and projects, including chart reviews, database development, and surveys, to ensure the objectives of the assignments/projects are met as directed by the Qualified Investigator/Principal Investigator, Manager, or designate.
  • Participate in preparing grant applications to a variety of internal opportunities and external grant funding agencies by coordinating meetings with investigators, drafting the application, researching literature that outlines the objective and background, methodology, and evaluation criteria of the trial to be approved by Qualified Investigator/Principal Investigator and Clinical Trial Team.
  • Maintain a clinical research program directory, request regular updates from Principal Investigators for existing entries, and add new study entries.
  • Prepare, organize, and maintain clinical trial research activities and assist the Qualified Investigator/Principal Investigator, Manager, or designate with financial tasks for trials or research studies in collaboration with the Clinical Trials Unit.
  • Respond to research cancer patient referrals, connect with patients by phone or in person to assess their consent status, and consent patients for research studies.
  • In collaboration with the Clinical Trials Team, determine the data requirements for specific projects, coordinate the data capture activities, and capture the clinical trials data according to the study protocol or project specifications.

Qualifications:

  • Graduation from a recognized Bachelor of Science program such as Biology or Physiology.
  • A minimum of one year of recent related experience, including experience coordinating a research project in an academic or health care setting, or an equivalent combination of education, training, and experience.

Core Competencies:

  • Understanding of Indigenous-specific racism and the broader systemic racism that exists in the colonial health care structure, with demonstrated leadership in breaking down barriers and ensuring an environment of belonging.
  • Ability to embed Indigenous Cultural Safety and Humility into all aspects of work, creating an environment where Indigenous patients feel respected, valued, and understood.
  • Commitment to ongoing education and training on Indigenous health issues, cultural safety, and DEI principles.
  • Ability to provide patient-centered care that respects and honors equity-deserving people’s perspectives on health and wellness.

For more detailed information and to apply, please visit the official job posting.

Expected salary: $40.94 – 51.1 per hour

Job date: Sat, 26 Apr 2025 03:31:36 GMT

IQVIA – Registered Dietician Clinical Trials Telehealth – Ontario, Canada – Ontario

Company: IQVIA

Location: Ontario

Expected salary:

Job date: Wed, 29 Jan 2025 03:27:47 GMT

Job description: Internal Job DescriptionJob Title: Registered DieticianLocation: Remote in the providence of Ontario, CanadaJob Type: Per DiemIQVIA are looking for experienced Dieticians to join our team. The ideal candidate will have experience in providing dietary advice and support to individuals with rare diseases.Key Responsibilities:Conduct nutritional assessments and develop personalized dietary plans for clients with rare diseasesProvide ongoing dietary counselling and support to clients and their familiesMaintain accurate and confidential client recordsParticipate in virtual team meetings and training sessionsRequirements:Qualified Registered Dietician with relevant certifications/registration or license in the providence registered and approved to practice.Experience in working with individuals with rare diseases is ideal but not essentialExcellent communication and interpersonal skillsAbility to work independently and remotely via telehealthIf you love helping others and are looking for a new challenge, look no further! Apply today!IQVIA est fière d’être un employeur offrant l’égalité des chances et nous nous engageons à créer un environnement diversifié et inclusif. Nous ne pratiquons aucune discrimination fondée sur la base de tout motif de discrimination interdit applicable, y compris, mais sans s’y limiter, la race, la religion, la couleur, l’origine nationale, le sexe, l’orientation sexuelle, l’âge, l’état civil ou le handicap. Des accommodements pour les candidats avec un handicap sont disponibles à toutes les étapes du processus de recrutement, sur demande. Si vous avez une déficience physique ou un handicap nécessitant un accommodement, nous vous encourageons à le divulguer lors du processus de recrutement afin qu’IQVIA puisse vous accommoder de manière appropriée.IQVIA est un fournisseur mondial de premier plan de services de recherche clinique, d’informations commerciales et de renseignements sur les soins de santé pour les secteurs des sciences de la vie et de la santé. IQVIA se consacre à accélérer le développement et la commercialisation de traitements médicaux innovants pour aider à améliorer les résultats des patients et la santé de la population dans le monde entier. Pour en savoir plus, visitezIQVIA is proud to be an equal opportunity employer and we are committed to creating a diverse and inclusive environment. We do not discriminate on the basis of any applicable prohibited ground of discrimination, including but not limited to race, religion, colour, national origin, gender, sexual orientation, age, marital status, or disability. Accommodations for applicants with disabilities are available at all stages of the recruitment process upon request. If you have a physical impairment or a disability that requires an accommodation, we encourage you to disclose this during the recruiting process so that IQVIA can appropriately accommodate you.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

Product Manager – Connected Home (Employee Market Trials) – Telus – Vancouver, BC

Company: Telus

Location: Vancouver, BC

Expected salary: $81000 – 121000 per year

Job date: Fri, 31 Jan 2025 05:46:52 GMT

Job description: closely with our engineers, marketing teams, industrial designers and manufacturing partners to guide products from conception… of innovation that empowers team members to solve complex problems and create remarkable human outcomes in a digital world. You’ll…

Worldwide Clinical Trials – Senior Specialist, Regulatory Compliance REMOTE CANADA – Ontario

Company: Worldwide Clinical Trials

Location: Ontario

Expected salary:

Job date: Fri, 17 Jan 2025 04:20:07 GMT

Job description: Who we areWe’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 WorldwideWe 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 Senior Specialist, Regulatory Compliance do at WorldwideThe Senior Specialist, Regulatory Compliance is a global position responsible for performing quality review and approval of essential documents in compliance with the relevant Standard Operating Procedures, country regulations and industry best practice prior to initiation of study sites. The Senior Specialist will assist in delivery of project timelines related to essential documents approval.What you will doAssume the functional role of the global Regulatory Compliance Lead for assigned projects, providing project team representation for the division.Develop Essential Document Review Plan (EDRP), Essential Document Review Requirements (EDRF), customize country Essential Document (ED) checklists project ED templates for use by the site activation or clinical operations team, as applicableProvides instruction/training to sponsor/CRO personnel on policies and procedures related to essential document collection and maintenance.Oversee and ensure Essential Document package review and approval for the project is in accordance with the relevant Standard Operating Procedures, Working Instructions, EDRP and EDRF.Receive, review, process and file essential documents, part of the Essential Document package agreed for the project, in accordance with applicable local regulations, internal SOPs and guidelines and EDRP.What you will bring to the roleExcellent organizational and time management skillsStrong planning, monitoring scheduling and critiquing skills.Good interpersonal skills, with ability to clearly and concisely present informationAbility to exercise sound judgment and ability to identify decisions requiring supervisory approvalExcellent spoken and written English language skills. Proven cross-functional team leadership skills and the ability to influence others at all levels of an organization.Your experienceUniversity degree preferred (Life Science desirable) and 3 years of relevant experience (1 year in similar role/position) or
Combination of education and 4 years of similar role/position (2 years of similar role/position) A bachelor’s degree in a technical field.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 ! For more information on Worldwide, visit or connect with us on .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’re on a mission to hire the very best and 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.

Research Assistant, Clinical Trials Phase 1 Unit – Providence Health Care – Vancouver, BC

Company: Providence Health Care

Location: Vancouver, BC

Job description: therapies! Reporting to the Research Operations Manager and receiving direction from the Research Coordinator(s), the Research… of the trial. Facilitates communication with personnel and participants to maintain project study flow. Maintains detailed…
This content provides information about a role in a research setting where the individual will assist in the coordination of clinical trials and communication with personnel and participants to ensure the smooth flow of the study. The Research Operations Manager and Research Coordinator(s) will provide direction and oversee the work. The individual is expected to maintain detailed records and provide support in various aspects of the research.
Job Description

We are looking for a dedicated and detail-oriented individual to join our team as an Administrative Assistant. In this role, you will be responsible for performing a variety of administrative tasks to support our team and ensure smooth operations.

Responsibilities:
– Answering phones, taking messages, and redirecting calls to appropriate personnel
– Managing and organizing documents, including filing, scanning, and copying
– Providing general administrative support, such as data entry, scheduling appointments, and ordering supplies
– Assisting in preparing reports, presentations, and other documentation
– Coordinating meetings, conferences, and travel arrangements
– Maintaining office supplies and equipment
– Other duties as assigned

Qualifications:
– High school diploma or equivalent
– Previous experience in an administrative role preferred
– Proficient in Microsoft Office Suite
– Excellent communication and interpersonal skills
– Strong organizational and time management skills
– Ability to work independently and as part of a team

If you are a motivated and reliable individual with a passion for administrative work, we would love to hear from you. Apply now to join our team!

Expected salary:

Job date: Fri, 06 Dec 2024 08:19:32 GMT

Clinical Research and Trials Coordinator – BC Cancer – Vancouver – Provincial Health Services Authority – Vancouver, BC

Company: Provincial Health Services Authority

Location: Vancouver, BC

Job description: range. For a specific trial or project, the Clinical Research and Trials Coordinator (CRTC) receives direction from the Qualified… Investigator/Principal Investigator, Manager, or designate to perform and organize special work assignments and projects. The…
Clinical Research and Trials Coordinator (CRTC) is responsible for receiving direction from the Qualified Investigator/Principal Investigator, Manager, or designate to perform and organize special work assignments and projects for a specific trial or project.
Position: Administrative Assistant

Location: Vancouver, British Columbia

Job Type: Full-time

Our client, a reputable company based in Vancouver, is seeking a dedicated Administrative Assistant to join their team. This role will involve providing administrative support to the office, assisting with various tasks, and ensuring the smooth operation of day-to-day activities.

Responsibilities:
– Answering and directing phone calls
– Managing and organizing files, documents, and records
– Assisting with data entry and processing paperwork
– Coordinating meetings and appointments
– Providing general administrative support to staff
– Handling incoming and outgoing correspondence
– Maintaining office supplies and equipment
– Other ad-hoc duties as required

Requirements:
– Previous experience in an administrative role is preferred
– Proficiency with Microsoft Office suite
– Excellent communication and organizational skills
– Ability to prioritize tasks and manage time effectively
– Strong attention to detail and accuracy

If you are a proactive individual with strong administrative skills and are looking for a new opportunity, please apply now for consideration.

Expected salary: $36.59 – 45.66 per hour

Job date: Sun, 17 Nov 2024 01:50:43 GMT

Clinical Trials Manager – University of Guelph – Guelph, ON

Company: University of Guelph

Location: Guelph, ON

Expected salary:

Job date: Thu, 31 Oct 2024 04:10:26 GMT

Job description: team, the Clinical Trials Manager will manage clinical trials conducted at the Ontario Veterinary College’s Health Sciences… project protocol is adhered to, the project is adequately resourced, and project deliverables are met. Providing leadership…

Research Project Manager, Clinical Trials Unit – BC Cancer – Vancouver – Provincial Health Services Authority – Vancouver, BC

Company: Provincial Health Services Authority

Location: Vancouver, BC

Job description: Research Project Manager, Clinical Trials Unit BC Cancer Vancouver, BC Working closely with the Principal… Investigator (PI) the Research Project Manager (PM) will assist with the development of research projects and contribute to the…
The Research Project Manager at BC Cancer in Vancouver works closely with the Principal Investigator to develop and contribute to research projects in the Clinical Trials Unit.
Title: Assistant Store Manager

Location: Woodstock, ON

Job Type: Permanent

Salary: $17.00 to $19.00 /hour

The Assistant Store Manager supports the Store Manager in the effective implementation of all store processes and operations to achieve company goals and objectives. Responsibilities include assisting in the supervision of staff, driving sales, ensuring high levels of customer service, and managing inventory.

Duties and Responsibilities:
– Provide exceptional customer service and ensure customer satisfaction
– Assist in the recruitment, training, and development of store staff
– Supervise and motivate employees to meet sales targets and KPIs
– Ensure store is clean, organized, and visually appealing
– Monitor inventory levels and assist with ordering and replenishment
– Manage cash handling procedures and reconcile daily sales reports
– Assist with store opening and closing procedures
– Address any customer complaints or issues in a timely and professional manner
– Assist with scheduling and managing employee hours

Qualifications:
– Minimum of 1-2 years of retail management experience
– Strong communication and interpersonal skills
– Ability to lead and motivate a team
– Proven track record of meeting sales targets and KPIs
– Strong organizational and time management skills
– Knowledge of inventory management and sales reporting
– Flexibility to work varied hours including evenings and weekends

If you are a motivated and results-driven individual with a passion for retail, we want to hear from you. Apply now to join our dynamic team!

Expected salary: $74618 – 107264 per year

Job date: Fri, 20 Sep 2024 00:19:52 GMT

Officer, Budget Development and Contracts, Provincial Clinical Trials Office – BC Cancer – Vancouver – Provincial Health Services Authority – Vancouver, BC

Company: Provincial Health Services Authority

Location: Vancouver, BC

Job description: development and Contracts reports to the Manager, Provincial Clinical Trials Office and Finance Administrator. The Officer… and contribute to strategic planning. The Officer is responsible for updating the project team, and internal and external…
The Officer is responsible for developing contracts and reports for the Manager, Provincial Clinical Trials Office and Finance Administrator. They also contribute to strategic planning and update the project team and internal and external stakeholders.
Job Description:
– Responsible for the day-to-day operations of a busy medical office
– Manage patient appointments, referrals, and medical records
– Provide administrative support to healthcare providers
– Answer phone calls, respond to emails, and greet patients
– Ensure a high level of customer service and patient satisfaction
– Maintain cleanliness and organization of the office
– Handle confidential patient information in a professional manner
– Assist with billing and insurance processes
– Collaborate with other staff members to ensure efficient operations
– Follow all privacy regulations and HIPAA guidelines.

Expected salary: $67861 – 97550 per year

Job date: Tue, 10 Sep 2024 22:15:57 GMT