Ri-24-008 Clinical Research Coordinator

2 weeks ago

Ottawa, Canada CHEO RESEARCH INSTITUTE Full time

**JOB DESCRIPTION**

**Posting #RI-24-008**

**Posting Period - February 22 to March 7, 2024**

**POSITION: Clinical Research Coordinator**

**TERM**: 1.0 FTE, 1 year contract with possibility of renewal

**SALARY**:Commensurate with skills & experience ($30.00/h to $36.00/hr)

**REPORTS TO**: Dr. Hanns Lochmüller

Children’s Hospital of Eastern Ontario Research Institute (“CHEO RI”) is the research arm of the Children’s Hospital of Eastern Ontario - Ottawa Children’s Treatment Centre (“CHEO”) and an affiliated institute of the University of Ottawa. CHEO is a beloved institution and workplace that is widely recognized for being an anchor in our community. CHEO RI works to create new knowledge and evidence to support CHEO in its provision of world-class care to our children. Our mission at CHEO RI is to connect exceptional talent and technology in pursuit of life-changing research for every child, youth, and family in our community and beyond.

**CHEO RI has an immediate requirement for a full-time (1.0 FTE) Experienced Clinical Research Coordinator.**

Due to recent funding success and expansion of our clinical trials team we have a need for a highly motivated Research Coordinator that will assist with research studies in children and adults with neuromuscular diseases. The Lochmüller Research group works across the translational spectrum and its activities include identification of novel NMD causative genes, using advanced cellular and animal models to determine mechanisms and test new compounds, large data sharing methodologies, clinical trials, and patient care.

**RESPONSIBILITIES**

Under the general supervision of Dr. Hanns Lochmüller, the Clinical Research Coordinator responsibilities will include:

- Responsible for the administration of the study or clinical trial.
- May be responsible for patient recruitment including screening and obtaining informed consents.
- Responsible for the creation of data forms and study procedure manuals
- Acts as key communicator between study personnel, and hospital staff in relation to the research projects they are managing.
- Responsible for supervision of the collection, scoring, and coding of research information.
- Will assist in the grantsmanship process including REB submissions.
- Training and supervision of study personnel.
- Perform work in accordance with the provisions of the Occupational Health and Safety Act and Regulations and all CHEO corporate/departmental policies and procedures related to Occupational Health and Safety.
- Prepare data for presentations and peer-reviewed research papers, and other administrative duties as required.
- Keep abreast of regulations and policies governing clinical research.
- Develop and monitor timelines for the research.
- Perform other related duties as assigned by supervisor.

**QUALIFICATIONS, SKILLs, AND ABILITIES**
- Bachelor’s degree in a Health Science discipline. (preferred)
- Minimum 3 years of research experience working in Clinical Research, preferably in management and administration of clinical trials. (Essential)
- Familiarity with clinical trial research, including REB requirements, Person Health Information Protection Act, and Good Clinical Practice Guidelines. (Essential)
- Proficiency in computer skills (Microsoft Office), database software packages, experience with online databases (e.g., REDCap) is an asset. (preferred)
- Superior communication (verbal and written), interpersonal and organizational skills. (Essential)
- Demonstrated collegiality, professionalism, and team skills. (Essential)
- Demonstrated initiative, flexibility, and ability to work independently. (Essential)
- Data management experience. (preferred)
- Strong analytical skills. (preferred)
- Bilingualism (English/French) is an asset. (preferred)

**WORKING CONDITIONS**
- Able to work in a dynamic, often hectic environment and be able to multi-task;
- Able to be flexible with working hours to meet deadlines and testing schedules;
- Clinic work within hospital settings; exposure to children and parents and/or caregivers, as well as adults.

**OTHER REQUIREMENTS**
- Eligible to work in Canada;
- Compliance with CHEO RI’s Universal COVID-19 Vaccination Policy; and
- Police Record Check.

**TO APPLY**

Applications will only be considered from those that are eligible to work in Canada. We thank all applicants for their interest; however, only those invited for an interview will be contacted.

**DESCRIPTION DE L’EMPLOI**

**Numéro d’affichage RI‑24‑008**

**Période d’affichage - du 22 février au 7 mars 2024**

**POSTE :Coordonnateur ou coordonnatrice de recherche clinique**

**DURÉE**: 1,0 ETP; contrat d’un an avec possibilité de renouvellement

**SALAIRE **:Selon les compétences et l’expérience (de 30 $/h à 36 $/h)

**RELÈVE DE**: Hanns Lochmüller

L’Institut de recherche du Centre hospitalier pour enfants de l’est de l’Ontario (« IR du CHEO ») est l’organisme de recherche du Centre

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