We are a vibrant, multi-disciplinary team of dedicated researchers focused on improving the health, treatment options and outcome for people and families living with MS. We will always consider the exceptional applicant, so if there’s nothing listed and you think you’ve got what it takes, feel free to send us your CV and cover letter outlining why you want to join our group and your proposed research area.
Contact: Dr Helen Tremlett. email: email@example.com
Currently Postings (2):
Job Title: Research Assistant/Technician 3 (Statistical Analyst)
Pay Grade: 4
Level Definition: TBC
Full-time or Part-time
Supervisor: Dr. Helen Tremlett
Location: S178-2211 Wesbrook Mall, UBC Hospital
Under general direction, the position is responsible for the performance of complex data programming and analyses related to varied biostatistical / epidemiological research.
▪ Reports directly to the Principal Investigator
▪ Interacts and works closely with the students, researchers and staff members of the Pharmacoepidemiology in MS (PiMS) research group. Particularly with the groups’ data analyst and biostatistician
▪ Maintains contact with other collaborating organizations, as required
CONSEQUENCE OF ERROR:
▪ Study may be jeopardized if not conducted according to ethical requirements as laid out by the University and by regulatory authorities
▪ Study files must be kept secured to ensure that patient confidentiality is not compromised
▪ An error within the realm of a research study may result in biased or incomplete data and skewed study results
The office is on the second floor of the Koerner Pavilion in the UBC Hospital with fluorescent lighting. There are no known hazards.
▪ Cleaning and manipulating linked administrative health and clinical data; creating variables suitable to be included in complex longitudinal models
▪ Conducting complex analysis and interpretation of results for ongoing studies funded by the US National Multiple Sclerosis Society, including, but not limited to: ‘Do the beta-interferons prolong life in people with multiple sclerosis?’; ‘Prodromal Multiple Sclerosis: The PrOMS Study’; ‘Adherence to Immunomodulators in Multiple Sclerosis: Prevalence and Clinical Impact of Multiple Sclerosis (The AIMS Study)’
▪ Facilitating data cleaning and coding within multiple sites across Canada; ensuring consistent or comparable approaches between sites
▪ Assisting with drafting papers for publication, specifically contributing to the methodology and results sections
▪ Providing support for other members of the PiMS team in their data analyses, as required
▪ Assisting with samples size calculations for the PiMS group to use in grant applications (in collaboration with other members of the group)
▪The incumbent will have the opportunity to exercise judgement, responsibility, and initiative on tasks pertaining to his/her work.
▪Works under minimum supervisory direction.
▪ University degree in a relevant discipline, such as Statistics, and a minimum of 3 years of related experience, or an equivalent combination of education and experience
▪ Demonstrated programming skills (such as using R function or SAS macro) and ability to perform data manipulation on large datasets using statistical software, including R, SAS and SPSS
▪ Working knowledge of research methodology, study design and statistical analyses
▪ Experience with health administrative data would be an asset
▪ Experience with, and knowledge about, special populations such as patients with chronic disease or multiple sclerosis would be an asset
▪ Appropriate knowledge of medical ethics
▪ Excellent interpersonal, oral and written communication skills
▪ Ability to exercise judgment and make decisions in accordance with the research objectives
▪ Ability to independently organize workload
▪ Ability to work in an interdisciplinary setting
Research Asst/Tech 3
The successful applicant will be responsible for coordinating the research efforts of a recently funded epidemiological research project spanning four provinces in Canada. The coordinating site is based at UBC. Tasks include ensuring consistency in the ethics applications across sites, overseeing the health-related data access requests in each province, and technical descriptions of the cohorts and data extraction. As the processes and data access differs by province, the successful individual will work closely with the relevant personnel within each province to ensure consistency across sites. The successful individual will also develop efficient methods of sharing information across sites, documenting decisions made, and ensuring the overall project keeps to the timelines and goals set. This will include arranging regular meetings between the sites including booking rooms, video conferencing, preparing agendas, recording minutes, performing literature reviews, coordinating references, facilitating submission of findings for publication and presentation at national and international conferences. Other specific interesting challenges will include access to emergency room visit data and ethnicity information (an exploratory aspect of the current study). The research coordinator will also support the overall efforts of the UBC group – the Pharmacoepidemiology in MS (PiMS) research group, with tasks ranging from facilitating grant submissions and publications through to supervising summer students and updating the groups website.
The Research Coordinator will report directly to the Supervisor, but will interact/work closely with the clinicians, staff members, students, post-doctoral fellows, data analysts and research associates of the UBC MS Clinic/PiMS Research Group as well as the other multi-disciplinary team members across Canada.
- Assist in the preparation, submission and coordination of ethics applications by summarizing study progress, uploading publications, and adding investigators as needed 10%
- Assist in the preparation and submission of grant applications (collating and formatting CV’s, uploading documents, obtaining letters of support) 10%
- Facilitate study protocol preparations (assist in the development, planning and organization of logistical study procedures)
- Oversee study logistics and implementation of study protocol
- Assist in preparation of research publications/presentations, including preparing and formatting figures and uploading documents for journal submission
- Conduct basic literature searches
Liaise and facilitate collaborations with health care professionals, research groups/researchers, and other supporting staff (coordinate studies with MS clinic – neurologists, receptionist, technicians; arrange teleconference calls with national contacts – e.g. StatsCan; liaise/coordinate with other universities for national multi-site project)
Provide administrative support to the BC MS Database Committee:
- Coordinate schedules and arrangements for the MS DB Committee meetings; send notices and reminders of meetings
- Prepare and distribute agendas for meetings; attend meetings, record and transcribes meeting minutes; prepare action items and oversee/facilitate completion of action items
- Assist with computer/technical issues and liaise with MedIT for technical support and for coordination and maintenance of network server/storage
- Provide support to research group offices including maintaining office supplies, computer hardware and software
- Assist in the supervision of directed studies students and summer students
- Prepare and update orientation manual for new, incoming research members
- Facilitate orientation of new members (access to the network, obtaining ID, office access (keys))
- Updating and maintaining the group’s website
Reports directly to the Supervisor.
Consequence of Error/Judgement
Any procedure or data record as part of a research study must be accurate and must accurately reflect the work performed. Studies may be jeopardized if not conducted according to ethical requirements as laid out by the University and by regulatory authorities. Study files must be kept secured or patient confidentiality may be compromised.
Undergraduate degree in a relevant discipline or Graduation from a technical college or institute. Minimum of 3 years related experience or the equivalent combination of education and experience. Previous experience with multi-site studies. Working knowledge of research methodology and design. Computer and web proficiency. Effective interpersonal and organizational skills, excellent oral and written communications skills. Ability to work both independently and within a team environment. Ability to work in an interdisciplinary setting. Attention to detail. Highly organized.
UBC hires on the basis of merit and is strongly committed to equity and diversity within its community. We especially welcome applications from visible minority group members, women, Aboriginal persons, persons with disabilities, persons of minority sexual orientations and gender identities, and others with the skills and knowledge to productively engage with diverse communities. All qualified candidates are encouraged to apply; however Canadians and permanent residents will be given priority.