Clinical Research Facilitator

Aventiv Research, IACT Health, LMC Manna Research, and True North Clinical Research have united to become the largest network of fully-owned and integrated clinical research sites in North America, Centricity Research. The sites that were formerly known as Aventiv operate in Ohio and Arizona and specialize in phase 1 pharmaceutical, device, and diagnostic...

Aventiv Research, IACT Health, LMC Manna Research, and True North Clinical Research have united to become the largest network of fully-owned and integrated clinical research sites in North America, Centricity Research. The sites that were formerly known as Aventiv operate in Ohio and Arizona and specialize in phase 1 pharmaceutical, device, and diagnostic...

Aventiv Research, IACT Health, LMC Manna Research, and True North Clinical Research have united to become the largest network of fully-owned and integrated clinical research sites in North America, Centricity Research. The sites that were formerly known as Aventiv operate in Ohio and Arizona and specialize in phase 1 pharmaceutical, device, and diagnostic...

The Clinical Study Associate (CSA) is an integral part of the study team, responsible for the creation, distribution and quality of clinical trial materials, tools and documents. The position supports the Clinical Study Manager and Data Management by tracking and reporting study metrics as well as by performing in-house office administrative activities to...

The Clinical Study Associate (CSA) is an integral part of the study team, responsible for the creation, distribution and quality of clinical trial materials, tools and documents. The position supports the Clinical Study Manager and Data Management by tracking and reporting study metrics as well as by performing in-house office administrative activities to...

**Clinical Research Coordinator I (RC I)** **Competition**: Clinical Research Coordinator I (RC I) **Program**: Bruyère Research Institute **Position Type**: 1 year contract with possibility of renewal **Salary Scale**: $$30.53 - $34.81/hour plus benefits **Main duties and responsibilities**: - Coordinate clinical trials studies in compliance with ICH...

**Research Coordinator 1** **Competition**: **Program**: Bruyère Research Institute **Position Type**: Casual, up to 15 hours/week for 6 months **Salary Scale**: $30.23 - $38.70/hour plus 8% in lieu of vacation & statutory holidays **Start Date**: As soon as possible **Closing Date**: 2 weeks from posting date **Job Location: Remote and Elisabeth...

**Tasks may include**: - Patient recruitment and follow-up, data collection, and data entry - Overseeing study start-up activities (approvals, contract, regulatory documents, training) internally for investigator-initiated trials - Maintaining current up-to-date regulatory binder/files - Facilitating physician oversight over study participants following GCP...

**Tasks may include**: - Patient recruitment and follow-up, data collection and data entry - Overseeing study start-up activities (approvals, contract, regulatory documents, training) internally for investigator-initiated trials - Maintaining current up-to-date regulatory binder/files - Facilitating physician oversight over study participants following GCP...

Conducting and overseeing various aspects of the Blueprint group, including: - Project management for the Blueprint research team - Preparing any required Research Ethics Board submissions - Preparing and maintaining budgets and/or timelines for funded and unfunded projects - Developing study protocols, surveys, and interview guides - Co-developing patient...

Projects in maternal-newborn care. The Clinical Research Assistant (CRA III) will assist in protocol and procedure manual development, database and case report form development, research ethics board submissions, assistance with regulatory and administrative management of clinical trials and other research projects. The (CRA III) will facilitate the conduct...

**The Ottawa Hospital: Inspired by research. Driven by compassion** The Ottawa Hospital Research Institute is the research arm of The Ottawa Hospital and an affiliated institute of the University of Ottawa. With more than 1,700 scientists, clinician investigators, trainees, and staff, and total revenues of more than $100 million, we are one of the foremost...

**Responsibilities for this position include, but are not limited to**: - Screen patients, obtain consent and enroll participants into studies, coordinate follow-up appointments as necessary - Track study compliance, update study logs and complete study forms - Conduct telephone follow-ups - Assist with data collection, data entry and data cleaning - Help...

Job title under revision The University of Ottawa—A crossroads of cultures and ideas The University of Ottawa is home to a dynamic community of over 50,000 students, faculty and staff, who live, work and study in both French and English. Our campus is a crossroad of cultures and ideas, where bold minds come together to inspire game-changing ideas. We...

Screen patients, obtain consent and enroll participants into studies, coordinate follow-up appointments as necessary. - Track study compliance, update study logs and complete study forms - Assist with data collection, data entry and data cleaning for Clinical Trials and investigator driven studies. - Manage all aspects associated with the Ottawa Health...

Dr. Pakhale and the community research center is seeking an experienced clinical research coordinator to assist with the overall operations of the community research office. **Tasks include, but are not limited to**: - Monitoring smooth functioning of community (peer) researcher training, recruitment, and implementation of research protocols - Maintaining...

The Ottawa Hospital Research Institute is seeking a highly skilled Clinical Research Coordinator to join their team. This exciting opportunity will be based in Ottawa, ON.Job SummaryThe ideal candidate will have at least 3 years of experience working in a clinical research environment and a post-secondary degree or diploma. They should also have extensive...

Assisting with the development of study protocols, surveys and interview guides - Screening studies and extracting relevant data for systematic reviews - Assisting with interview and survey studies - Co-developing patient engagement strategies and coordinating engagement - Designing and facilitating educational workshops and resources - Assisting with...

p>We are seeking a well-trained clinical researcher or research coordinator with demonstrated expertise in clinical research in the area of sleep and/or neurosciences. This work will involve interdisciplinary project development and management on sleep phenotyping in various clinical populations (with a focus on brain-heart interactions) and investigating...

**Major responsibilities include**: - Recruit, consent, and coordinate visits for research participants, as appropriate to specific study procedures. - Establish and coordinate logístical arrangements for research participants and recruitment activities, as appropriate to the study. - Data collection, data entry (including use of REDCap and transcription...