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Program Assistant, Department Of Evaluation & Research Services
Company | Fraser Health Authority |
Address | Surrey, British Columbia, Canada |
Employment type | FULL_TIME |
Salary | |
Category | Hospitals and Health Care |
Expires | 2023-08-06 |
Posted at | 10 months ago |
Fraser Health is responsible for the delivery of hospital and community-based health services from Burnaby to Fraser Canyon on the traditional, ancestral and unceded territories of the Coast Salish and Nlaka’pamux Nations, and is home to six Métis Chartered Communities.
- Responds to requests for information regarding departmental policies and procedures and conveys a response either directly or by correspondence and/or refers individuals to appropriate contacts for specific information as required.
- Arranges internal/external meetings as required by booking rooms, notifying participants, confirming attendance, ordering catering, preparing agenda, conferences and seminars; prepares and distributes handouts and overheads. Records, prepares and distributes minutes and agenda; follows up on action items as required. Makes travel arrangements as necessary; maintains and organizes appointment calendars.
- Maintains budget for the Research Department. Calculates and prepares Administrative Overhead fee invoices, processes payments; records, tracks and follows up on outstanding accounts. Ensures expense claims for FH researchers with grants are processed properly for sign off by the Director. Administers the financial requirements of the DERS research seed grant program. Runs GL/Financial reports from Meditech to identify all costs charged to DERS to maintain ongoing analysis of monthly variance.
- Performs a variety of word processing duties such as typing correspondence including reports, letters, memoranda and emails; prepares charts and tables, presentation material, and newsletters from rough draft and/or general instructions.
- Researches support materials for conducting research; gathers and consolidates this material into resources inventory. Communicates with FH and FH affiliated researchers to obtain research summaries, obtain abstracts from online publication databases for upload to Research Study database.
- Coordinates the workflow for the assigned area; develops and implements new work methods and procedures; identifies problems; recommends alternative solutions and implements approved changes. Contributes to the development of new standard operating procedures, (e.g., Grant Administration, Research Impact). Revises old standard operating procedures, ( e.g., SOPs for Affiliated Researchers, Contract Review). Develops SOP for data entry to Research Administrative database.
- Coordinates DERS contracts with vendors and HSSBC and prepares associated Purchase Requisitions.
- Compiles statistical records on departmental activity by utilizing computer spreadsheet and database applications; prepares background information by researching, gathering and checking data and developing appropriate links and formulae for spreadsheets and databases; summarizes information and generates reports using word processing and presentation graphics software applications. Runs administrative reports using Report Builder for annual reporting.
- Receives information and documents to create files for Research Ethics Applications, Clinical Trial Agreements and other research Agreements related to, industry sponsors, FHA and affiliated investigators and other external funders. Assesses that all information is complete prior to data entry by comparing submitted ethics applications/executed contracts/agreements to ensure compliance with standard requirements. Enters requisite information into database(s)/spreadsheets for relevant department activities. Tracks the contract review/agreement process; follows up with sponsors, investigators and others as required to obtain information needed for processing Clinical Trial Agreements and their budgets. Ensures contracts and collaboration agreements are completely signed off and routed to appropriate FH, industry, and/or academic signatories.
- Performs record management duties for all research studies submitted for ethical review, Clinical Trial agreements and other research Agreements; sets up and maintains secure numeric, alphabetical and subject filing systems/indexes.
- Revises forms as directed for the Research Department.
- Ability to operate a personal computer and apply a variety of software applications.
- Ability to operate related equipment.
- Demonstrated ability to organize and prioritize work in an environment subject to changing deadlines, stress and interruptions.
- Ability to work independently using initiative and judgement with limited direction.
- Physical ability to perform the duties of the position.
- Ability to type 60 wpm
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