About the Opportunity
Reporting to the Principle Investigator (PI), the Research Assistant contributes to management of projects through the PI's work with the Nova Scotia Early Psychosis Program (NSEPP). The research assistant will support work flow of a new study investigating MRI and EEG findings in relation to response to antipsychotic medication in early psychosis patients. The research assistant will also support other projects involving neuroimaging in early psychosis patients, as well as a project comparing functional outcomes in two commonly used long acting injectable antipsychotic medications. Specific tasks of the Research Assistant would include :
Study Administration
- Regular meetings with Dr. Dempster to provide updates on the progress of the research studies
- Processes & submits forms to Research Ethics Board (REB)
- Accompanies research participants to MRI and EEG studies
- Coordinates research participants bookings for MRI and EEG studies
- Contacts study subjects to book diagnostic / clinical tests, assessments and appointments
- Administers, scores & records results for study tests (e.g. questionnaires)
- Assists with subject screening by contacting clinical care teams
- Conducts informed consent discussions with patients who have agreed to be contacted for research purposes
Administrative Support
Acts as a point of contact by providing information or direction when answering, screening & referring telephone calls, emails, faxes and / or in-person inquiriesReplies to routine correspondence & composes and edits letters, documents & general memorandaAttends team meetingsData management
Collects data related to studiesMaintains filing systems for subject & study documentationFiles study documents, test results, etc.Develops & maintains methods of tracking information through databases and spreadsheetsEnters, summarizes & analyses data using database and / or spreadsheetsArchives documentation related to study once it has closed & develops & maintains a method of retrieval from storageCoordinates booking of return study visits, arranges data transfer and secure storage of dataFollows up with clinical care teams regarding patients enrolled in research studiesAssist with searching publication databases for literature related to the study and maintaining a database of publications locatedOther related duties as required.
About You
We would love to hear from you if you have the following :
Currently enrolled in post-secondary education in a Health Science and / or Science related field requiredCompleted post-secondary education in a Health Science and / or Science related field preferredTwo years’ research related experience preferredTCPS2 : CORE Certification considered an assetCCRP (Certified Clinical Research Professional) or CCRA (Certified Clinical Research Associate) an assetProficiency in MS Office (Word, Access, Excel, PowerPoint), email and internetEffective communication, problem solving and decision making skillsAbility to draft, format and edit office correspondenceWell developed organizational, time management and daily planning skillsAbility to work well independently as well as within a multi-disciplinary team environmentSkills and experience in promoting learning cultures that nurture equity, diversity and inclusivity with a focus on intersectional values, analysis, and actions, clinical humility, and the responsible use of power and privilege.Previous experience in a health care / research setting is an assetSuccessful Applicants are required to provide a criminal record check (including Vulnerable Sector Search) to Human Resources before starting employment and assume any associated costs as a condition of employment.PLEASE NOTE : Applicants will be screened on the above qualifications. Applicants must clearly demonstrate how they meet the knowledge and competencies in their cover letter and resume. Applicants relying on education and experience equivalencies must demonstrate such equivalencies in their application. Applicants will not be considered for an interview if applications are incomplete or missing information.
Hours of Work
3 year Long Assignment, Full-Time (75 hours bi-weekly)
Beginning July 15, until July 15,
Dates are approximate and are subject to change.Compensation and Benefits
22.34 - $27.92 Hourly
43,.98 - $54,.92 Annually
Successful candidates may be eligible for our benefits package which includes health, dental, travel, long-term disability, and life insurance coverage as well as a defined benefit pension plan.