Research Project Coordinator II
- Hamilton, ON, Canada
Full-time
Applications open in a new tab.
Job details
- Job type
- Full-time
- Apply by
- Experience
- Minimum 2 years’ experience in multi-centre research studies or equivalent experience.
- Posting language
- English
- Posted
Original job description
The Research Project Coordinator II coordinates and assists with the overall coordination in all aspects of a clinical study at PHRI. Responsibilities include: Plan study meetings and teleconferences including scheduling, tracking of attendee responses, assisting with travel arrangements if required and creation of meeting materials. Provide training and administer site management expectations to staff;. Track ongoing site IP usage and quantities using IP management system and/or supporting spreadsheets, shipments and create IP usage projection reports; Support the design and creation of outcome event adjudication forms and documents including event adjudication manual, event adjudicator training, decision forms, and reports; Coordinate site start-up process; Review and provide input and necessary documents for regulatory applications; oversee the management and reporting of data; Design, creation, requesting, and testing/validation of reports;.and support the implementation of various study management plans
- Undergraduate Degree in Biology, Health Sciences or Health Studies.
- Minimum 2 years’ experience in multi-centre research studies or equivalent experience.
- Experience with the management of large research datasets, preferably clinical data.
- Working knowledge of ICH-GCP Guidelines and international research requirements.
- Highly efficient computer skills, experience with the Microsoft Office suite, and electronic data capture systems such as iDataFax or TrialMaster.
- Broad knowledge of research methodology, clinical trials, and drug development processes.
- Highly developed communication skills including the ability to problem solve and think critically.
More about this job
Responsibilities
The Research Project Coordinator II manages clinical study logistics, including site start-up, meeting coordination, and IP usage tracking. They also oversee data reporting, regulatory documentation, and the creation of outcome event adjudication materials.
Requirements
Candidates must hold an undergraduate degree in Biology, Health Sciences, or Health Studies and have at least two years of experience in multi-centre research. Proficiency in ICH-GCP guidelines, clinical data management, and electronic data capture systems is required.
Skills
- Clinical study coordination
- Site management
- Regulatory applications
- Data management
- ICH-GCP guidelines
- Research methodology
- Clinical trials
- Drug development
- Microsoft Office
- Electronic data capture
- iDataFax
- TrialMaster
- Communication
- Problem solving
- Critical thinking
Visa sponsorship
Not detected in the job text
Categories
- Science & Research
- Healthcare
- Administrative
Keywords
- Clinical study
- PHRI
- IP management
- Outcome event adjudication
- Regulatory applications
- Data management
- ICH-GCP
- Research methodology
- Clinical trials
- Drug development
- Microsoft Office
- Electronic data capture
- iDataFax
- TrialMaster
- Multi-centre research
- Site management