Research Associate, Research, Innovation

2 weeks ago


Halifax, Canada Nova Scotia Health Authority Full time

**Req ID: 146677**
**Company: Nova Scotia Health**
**Location: Central** **Zone, Centennial Building - QEII**
**Department: RSH Ophthalmology**
**Type of Employment: Casual** **Hourly FT long-assignment** (100%** **FTE) x 1** **position(s)**
**Status**:Management/Non-Union** Position**
**Posting Closing Date: 15-Mar-23**
- **This is a reposted position. Current applicants are not required to re-apply.**

Nova Scotia Health is the largest provider of health services in Nova Scotia, with some specialized services also offered to clients throughout Atlantic Canada. We’re on a mission to achieve excellence in health, healing and learning through working together, which is reflected in the hospitals, health centres and community-based programs we operate across the province. Our passionate team of professionals provides a variety of high-quality inpatient and outpatient services including academic, tertiary, and quaternary care, as well as continuing care, primary health care, public health, and mental health and addictions. Join a diverse team of innovators, collaborators and creative thinkers today.

Nova Scotia Health’s Research, Innovation and Discovery portfolio is transforming health care delivery and improving the health of all Nova Scotians by leading initiatives that deliver high-impact health care solutions and developing strategic partnerships with clinical champions, industry, healthcare foundations, governments and academic partners. By pairing leading researchers, innovators, and clinicians with entrepreneurs through our newly formed Health Innovation, Research and Discovery Hub, their creative solutions are improving health and health care while also contribute directly to Nova Scotia’s economy.

**Responsibilities**:
Responsibilities include:

- Conducts focus groups and interviews as per study protocol
- Maintains communication with Research Ethics Board (REB) throughout the study
- Confers with the PI or Research Manager on project/study progress, compliance and interpretation
- Assists in orienting new Research staff as required
- Implements study methods as per protocol
- Manages Case Report Forms and study questionnaires and ensures their accuracy and completeness
- Liaises with the research team for each project
- Conducts systematic reviews of the literature
- Assists in report composition
- Plans, develops and co-ordinates projects in consultation with key stakeholders
- Participates in the development and analysis of grant funded study protocols
- Prepares documents for the submission to the REB for study/project approval and closure
- Participates in submission of grants to funding agencies
- Develops consent forms in consultation with REB and the sponsor
- Confers with the Director and sponsor representatives on project progress, compliance and interpretation
- Identifies relevant dissemination opportunities
- Enters and summarizes data and uses database and/or spreadsheets
- Liaises with programmers on production of required data sets
- Maintains, stores and retrieves study documentation
- Conducts qualitative analysis under supervision
- Sees patients per study requirements, working with associated physicians, performing visual testing, and other non-invasive tests as required
- Maintains research accounts for studies within area of responsibility and monitors study expenditures
- Coordinates and monitors study timelines and study visits with patient, doctor and other services

**Qualifications**:
We would love to hear from you if you have the following:

- Bachelor’s degree in a health sciences or social sciences discipline (e.g. epidemiology, community/public health, biostatistics or health economics)
- CCRP or CCRA an asset
- Medical Terminology course preferred
- Good Clinical Practice training preferred
- Current registration with the relevant professional healthcare licensing organization desirable
- Familiarity with health records
- Strong organizational and communication skills
- Strong report writing skills
- Effective interpersonal, communication and teaching skills
- Demonstrated time management and organizational skills
- Effective research and analytical thinking skills
- Strong negotiation, conflict resolution and rapport-building skills
- Ability to work well independently as well as within a multidisciplinary team environment
- Minimum of two years research experience
- Previous Health Canada regulated clinical trial research experience strongly preferred
- Successful 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.**Hours of Work**:
Long Assignment Full-Time; 75 hours bi-weekly
Beginning April 3, 2023 to April 3, 2024

**Salary Information**:
$26.82 to $33.53 hourly

$52,299.59 to $65,374.34 annual salary

**Once You've Applied**

As per the COVID-19 Mandatory Vaccination Protocol in High-Risk Settings, Nov



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