Your Opportunity:
Are you an experienced clinical trial professional looking to work with cutting-edge cancer therapies? We are seeking a dynamic Clinical Trials Coordinator to join our Clinical Trial Unit (CTU), with a primary assignment to the Genitourinary (GU) group. Reporting to the CTU Associate Manager, you will work in a team environment to facilitate clinical trial activities and complete delegated study tasks. While your daily focus will highlight ongoing study conduct, patient data management, and monitoring/inspection readiness, all coordinator positions maintain a general scope and may be reassigned to, or assist, other teams within the Unit as operationally required.Building strong relationships is key, as you will serve as a central study point of contact for PIs & study staff, internal CCI departments, outside hospitals, and external agencies (, Sponsors, CROs, and Health Canada). Operationally, you will coordinate study visits—from site selection through to close-out—while managing regulatory documentation and liaising with industry partners for day-to-day study specifications. To ensure efficiency, you will create and update systems to track workflows, regulatory documentation, and data/ethics submissions. Responsibilities may also include reviewing source documents, abstracting protocol data to complete CRFs, and resolving data queries. You will track study metrics, coordinate monitoring visits, and assist with site audits and regulatory inspections. Additionally, you will manage patient study registration, notify personnel of assigned treatments, relay adverse drug reaction reports, and ensure all required safety documentation is completed. If you are a detail-oriented professional with a passion for oncology research, we want to hear from you!
Description:
As a Clinical Research Coordinator, you will provide support for research studies through the identification, collection, and reporting of clinical trial data. You will compile research, reports and regulatory documents as required by the protocol, and study/sponsor. This involves ensuring research information is timely, accurate, valid, meaningful, and to the sponsor's satisfaction, and that studies are run according to local and global regulations.
Required Qualifications:Completion of a minimum two year diploma or certificate in a health care related field. Minimum of two years' clinical research experience.
Additional Required Qualifications:Oncology knowledge and general clinical trial experience required; experience with genitourinary (GU) cancer/disease or trials is an asset. Prior experience working with pharmaceutical sponsors. An ability to multi-task effectively in a busy area with multiple interruptions and competing demands. Knowledge of oncology medical terminology, anatomy and tumor staging. ICH-GCP training and familiarity with clinical trial regulatory reporting requirements. Excellent computer skills and experience working with Microsoft Office programs. Familiar with using and creating spreadsheets, and using various databases ( InForm, RAVE). Experience with electronic medical records ( Netcare, ARIA, Connect Care), and ethics submission systems (IRISS, REMO). Must be able to transport large volumes of materials (study supplies, charts, boxes, etc.) to various areas regularly and push/pull loaded carts. Physical demands of the job include sitting for extended periods, pushing heavy carts, lifting boxes of documents/office/medical supplies and equipment weighing up to 40 lbs., and using repetitive motions, lifting, bending, reaching and standing for prolonged periods. To ensure your skills and qualifications are considered, please attach a resume and cover letter with your application indicating how your education and experience meet the requirements of this position.
Preferred Qualifications:Preference given to those with a bachelor’s level degree (health-related). Completion of an approved Clinical Research or Data Management Certificate Program. SoCRA or ACRP certification/membership.
Clinical Research Coordinator - Genitourinary Group • Edmonton, Edmonton Zone
Join Amaris Consulting as a Country Clinical Studies Manager in Canada.Lead the lifecycle of clinical trials while ensuring operational excellence and compliance.This remote role involves managing ... Voir plus
Superprof is Canada's #1 tutoring platform, and we're actively recruiting passionate tutors! Whether you're a student, a professional, or simply someone who loves teaching, join the largest communi... Voir plus
Working in a LASIK MD clinic (an affiliated entity of Vision Group) is to help improve people's eyesight.It is having the feeling of a mission accomplished and a job well done.It is seeing happines... Voir plus
Embark on a purpose-driven career as a Clinic Coordinator with MaKami College.Facilitate the booking and scheduling process while overseeing the Student Clinic for aspiring massage therapists.In th... Voir plus
Work in a purpose-driven career with MaKami College, a public post-secondary college that has been helping students for over 20 years with locations in Edmonton and Calgary, Alberta.MaKami College ... Voir plus
Care Coordinator – Lifemark Health Group.Sherwood Drive, Sherwood Park, AB, T8A 3X3.The Care Coordinator is responsible for fostering a strong relationship between the clinic and its customers, inc... Voir plus
Looking for people to participate in taking online surveys for Fortune 500 brands.All you need to do is complete online surveys by sharing your opinion.You will help influence brand decisions on se... Voir plus
Looking for people to participate in taking online surveys for Fortune 500 brands.All you need to do is complete online surveys by sharing your opinion.You will help influence brand decisions on se... Voir plus
A nonprofit organization based in Mount Pearl seeks a Volunteer Coordinator to manage onboarding, support, and project matching for volunteers.This remote role requires strong people skills and exp... Voir plus
The Family Centre is seeking a highly qualified Clinical Supervisor with advanced clinical expertise and leadership experience, specializing in trauma-informed approaches.You will oversee therapeut... Voir plus
Lead the genetics and genomics laboratory services in Alberta as Provincial Medical-Scientific Director.Oversee quality initiatives and partner with clinical leaders for impactful healthcare.In thi... Voir plus
A leading recruiting firm is seeking a Clinical Researcher with a PhD for a part-time remote role.You will contribute expertise to AI projects, including designing legal workflows and evaluating AI... Voir plus
A leading global CRO is seeking a Senior Lead Clinical Data Manager to act as the primary client contact for deliverables.This role requires strong leadership and project management skills, with ex... Voir plus
Month Term with possibility of extension.Until successful candidate is found.As the largest not-for-profit provider of seniors’ care in Alberta and British Columbia, The Good Samaritan Society and ... Voir plus
Position Type: Permanent Full-Time (40 hrs/week).We specialize in orthodontics and pediatric dentistry, offering personalized and comprehensive care for patients of all ages.Our dedicated team of r... Voir plus
Location: 12308 111 Avenue #200, Edmonton, Alberta.Closing Date: Until suitable candidate found.Position Status: Full Time (40 hours per week), Permanent.Reporting to the Children & Family Services... Voir plus
What if you could redefine what’s possible? With us, you can.We are the home of ambitious, passionate, and innovative world shapers.With an unmatched breadth and depth of engineering, advisory and ... Voir plus
This range is provided by HelixRecruit.Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.This opportunity is shared as part of a referral program.... Voir plus
A leading remote job provider is looking for an Outsourcing Coordinator to join their team.This part-time position focuses on content development, research, and ensuring quality across various digi... Voir plus
A clinical research consultancy in Canada is seeking a research coordinator to manage and oversee clinical trials.Candidates should possess a degree and have 2-3 years of relevant experience.Succes... Voir plus
