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Senior Clinical Research Coordinator Jobs

Senior Clinical Research Associate - Oncology - Montreal
By ICON Strategic Solutions At Montreal, Quebec, Canada
2+ years of clinical monitoring experience required. 5 yrs of clinical monitoring preferred
Knowledge of ICH and local regulatory authority regulations regarding drug (PREFERRED)
8 - 10 visits/month, combo of on site and remote visits
Monitoring Oncology and Multi -Therapeutic studies
B.A./B.S. with strong emphasis in science and/or biology preferred (but not required)
Research Coordinator Non-Clinical Jobs
By Nova Scotia Health Authority At Halifax, Nova Scotia, Canada
Demonstrated time management and organizational skills
Knowledge of medical terminology and clinical trial regulatory guidelines
Knowledge of bookkeeping and familiarity with health records
Effective interpersonal and communication skills
Demonstrated research and analytical thinking skills
Assists to develop educational/promotional material for the study/department
Research Coordinator Non-Clinical Jobs
By Nova Scotia Health Authority At Sydney, Nova Scotia, Canada
Demonstrated time management and organizational skills
Relevant clinical experience considered an asset
Experience with RedCap considered an asset
Database construction and maintenance skills
Effective interpersonal and communication skills
Demonstrated research and analytical thinking skills
Clinical Research Coordinator, Cardiac Sciences
By University of Calgary At Calgary, Alberta, Canada
Demonstrated strong organizational and time management skills
Screening, enrolment, management and retainment of study subjects
Demonstrated technical dexterity, knowledge and skills in MS Office and electronic data collection and reporting
Management and Staff Careers website
Coordination of all personnel and services required to meet protocol requirements
Data collection, storage and data entry per protocol and all governing regulations
Clinical Research Coordinator Jobs
By IMPART At Halifax, Nova Scotia, Canada

Key Job Responsibilities: • Printing of supporting documents for study recruitment • Enrollment/recruitment of participants from study sites and follow-up with patients through phone/face-to-face ...

Clinical Research Coordinator Ii (Multiple Vacancies)
By Rutgers University At New Brunswick, Canada
Maintain documentation according to protocols, standard operating procedures, and FDA requirements.
This role requires strong organizational and prioritization skills, as the coordinator will be responsible for managing 4 to 5 concurrent trials.
Excellent interpersonal skills are essential for clear and confident patient interactions.
Experience in cardiology and complex clinical trials is a plus.
Physical Demands: Standing, sitting, walking, talking or hearing. No special vision requirements. Lifting (up to 25 pounds).
* Do you have experience in cardiology and complex clinical trials?
Clinical Research Coordinator, Department Of Medicine
By University of Calgary At Calgary, Alberta, Canada
Proficient organizational, time management and problem-solving skills
Knowledge and experience with ICH-GCP requirements, HIA, PIPA, FOIP, TCPS2
An understanding and experience with Clinical Trial Management and data capture systems
Management and Staff Careers website
Minimum of 3-5 years of relevant work experience in clinical research in an academic setting including experience coordinating clinical research trials
Experience in hemodialysis, nephrology, and transplant-related care an asset
Clinical Research Coordinator (Crc)
By Centricity Research At Brampton, Ontario, Canada
Knowledge of general research procedures and regulatory requirement is an asset
To be knowledgeable of the protocol so that all study activities are completed correctly
Provide lifestyle adherence counseling & general training / education to study participants, as required by protocol
To monitor and report all adverse experiences and abnormal results to the Investigator, Sponsor and IRB if necessary
Bachelor of Science degree or related degree, or 2 years’ minimum experience in healthcare or clinical research required
Experience working with geriatric patients and patients with dementia is a strong asset
Research Coordinator (Non-Clinical) Jobs
By Nova Scotia Health Authority At Halifax, Nova Scotia, Canada
Demonstrated time management and organizational skills
Completion of a relevant Bachelor’s degree or an equivalent combination of education, training and experience
Assists to develop educational/promotional material for the study/department
As per the study protocol requirements, obtains and/or verifies medical and family history
Relevant clinical experience considered an asset
Effective interpersonal and communication skills
Clinical Research Coordinator, Ccfv
By IWK Health At Halifax, Nova Scotia, Canada
Excellent time management skills and experience
Demonstrate a high level of time management and decision-making skills regarding setting priorities based on deadlines (both internal and external)
A minimum of 2 years’ nursing experience with strong clinical skills
Assess the staff requirements (nurses, research assistants) for pre-study preparation, recruitment, enrollment follow-up
Experience in a clinical trial environment strongly preferred
Basic knowledge in research and/or project accounting systems strongly preferred
Non-Clinical Research Coordinator, Ccfv
By IWK Health At Halifax, Nova Scotia, Canada
Excellent time management skills and experience
Degree or diploma in a related health profession or an equivalent combination of education, training and/or experience may be accepted
Experience in a clinical trial environment strongly preferred
Basic knowledge in research and/or project accounting systems strongly preferred
Excellent oral and written communication skills
Excellent knowledge of Microsoft Office (Word, Excel, PowerPoint, Access, MS Project), Adobe Acrobat, WordPress, and social media platforms
Research Coordinator - Evaluative Clinical Sciences Platform - Temporary Full Time (2023-4756)
By Sunnybrook At Toronto, Ontario, Canada
Excellent coordination and project management skills, including ability to coordinate multiple studies, perform concurrent tasks, and work under time constraints
Detail-oriented with excellent organization and time management skills
Overall efficient day-to-day management of assigned research studies including maintenance of study documentation
Completion of a postsecondary degree (master’s degree preferred) in a health-related field, or an equivalent combination of education, training, and experience
Working closely with senior research team members to further develop research skills
Excellent community outreach, collaboration, engagement, and relationship building skills
Clinical Research Coordinator (Crc)
By Centricity Research At Toronto, Ontario, Canada
Knowledge of general research procedures and regulatory requirement is an asset
To be knowledgeable of the protocol so that all study activities are completed correctly
Provide lifestyle adherence counseling & general training / education to study participants, as required by protocol
To monitor and report all adverse experiences and abnormal results to the Investigator, Sponsor and IRB if necessary
Bachelor of Science degree or related degree, or 2 years’ minimum experience in healthcare or clinical research required
Experience working with geriatric patients and patients with dementia is a strong asset
Senior Advisor, Clinical Jobs
By Ontario Health | Santé Ontario At Toronto, Ontario, Canada
Strong knowledge of project management
Superior attention to detail, organization, and time management skills, with ability to prioritize and manage multiple projects.
Excellent interpersonal and relationship-building skills, with demonstrated experience engaging and building relationships and consensus among diverse stakeholders.
Premium defined benefit pension plan
Lead and contribute to knowledge transfer and exchange activities within and outside team
Create guidelines for developing education materials and staff development
Clinical Research Coordinator Jobs
By Headlands Research At Greater Toronto Area, Canada
Experience with CRIO (Clinical Trial Management System) is a plus
Experience and training in conducting clinical trials with knowledge of ICH GCP
Recruit and screen study subjects according to specific protocol requirements
A thorough understanding of regulatory requirements
Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
Experience with administering vaccines is a plus
Research Coordinator - Evaluative Clinical Sciences Platform - Temporary Full Time (2023-4359)
By Sunnybrook At Toronto, Ontario, Canada
Time management skills: ability to prioritize workload and flexibility to adjust to changing work plans, schedules and deadlines
Liaise with study team members to ensure high standards of quality and optimal management of research participant care
Experience with chart review and data entry
Manage process for Data Sharing Agreements / contracts
Two-to-five years experience in a clinical research setting, recruiting participants into multiple studies.
Strong Interpersonal skills and ability to maintain professional communication and healthy relationships with staff, research participants and their caregivers
Research Coordinator (Non-Clinical) - Orthopaedics Research, Ri&D
By Nova Scotia Health Authority At Halifax, Nova Scotia, Canada
Demonstrated time management and organizational skills
Relevant clinical experience considered an asset
Effective interpersonal and communication skills
Demonstrated research and analytical thinking skills
Previous experience in a relevant field preferred
Strong negotiation, conflict resolution and rapport-building skills
Research Coordinator (Non Clinical) - Department Of Surgery, Ri&D
By Nova Scotia Health Authority At Halifax, Nova Scotia, Canada
Demonstrated time management and organizational skills
Relevant clinical experience considered an asset
Experience with RedCap considered an asset
Database construction and maintenance skills
Effective interpersonal and communication skills
Demonstrated research and analytical thinking skills
Clinical Research Coordinator Jobs
By Centricity Research At Vaughan, Ontario, Canada
Communicate study questions to the Investigators/Research Management/other CRPs
Maintain professional relationships with study participants, physicians, industry representatives and vendors of trial management
Assist the Research Management and Investigators with any other research tasks as required
Be knowledgeable of study protocol to ensure all study activities are completed correctly
Collect and report all adverse events and abnormal results to the Investigator, Sponsor, and REB as per protocol and REB requirements
Experience working in a health care environment e.g. blood pressure sphygmometers, automated blood pressure machines, weight scales, and ECG machines
Clinical Research Coordinator Jobs
By Michael Garron Hospital At Toronto, Ontario, Canada
Experience with computer data management and analysis software including REDCap™, SPSS™, preferred.
Knowledge and experience in obtaining informed consent for research studies.
Knowledge and experience in administering survey instruments.
Decisions require keen judgment, careful consideration and intimate knowledge of hospital operations and organizational structure
Certification as a Clinical Research Professional is an asset
Minimum 3 years’ experience in clinical research required.