Category Archives: Alumni

ORISE: Pandemic Data Fellowship, Post-Master’s

Category : Alumni

Description

A fellowship opportunity is available in Community Interventions for Infection Control Unit (CI-ICU), Division of Global Migration and Quarantine (DGMQ), National Center for Emerging and Zoonotic Infectious Diseases, at the Centers for Disease Control and Prevention (CDC) in Atlanta, Georgia.

The fellow will train with DGMQ, CI-ICU on development of public health programs for pandemic influenza planning, preparedness and response as well as evaluation of public health projects, epidemiological investigations, and literature reviews.  This training will include assessing the feasibility, acceptability, and impact of school closures and other nonpharmaceutical interventions; reporting performance measures for science, policy, and communication activities; monitoring dissemination of the non-pharmaceutical guidance for pandemic influenza preparedness and response for state and local health department usage; developing materials used in unit and/or CDC-wide events and activities for use in public health policy or communication; and collaborating with epidemiologists, health scientists, health communicators, and medical officers.

Specific opportunities may include:

•Managing, analyzing, classifying, and presenting data on unplanned school closure announcements that were collected through online systematic searches using an automated data capturing system.

•Comparing the unplanned school closure data that were collected by different methodologies.

• Applying new technology such as machine learning to modify the existing system to reduce the noise level in the data.

• Cleaning, formatting, evaluating, and analyzing qualitative and quantitative data.

• Conducting literature reviews on nonpharmaceutical interventions.

This program, administered by ORAU through its contract with the U.S. Department of Energy to manage the Oak Ridge Institute for Science and Education, was established through an interagency agreement between DOE and CDC. The initial appointment is for one year, but may be renewed upon recommendation of CDC contingent on the availability of funds. The participant will receive a monthly stipend commensurate with educational level and experience. Proof of health insurance is required for participation in this program. The appointment is full-time at CDC in the Atlanta, Georgia, area. Participants do not become employees of CDC, DOE or the program administrator, and there are no employment-related benefits.

Click HERE to apply


CDC Surveillance Epidemiologist, due 3/15

Category : Alumni

A fellowship opportunity is available within the Influenza Division (ID) Epidemiology and Prevention Branch of the National Center for Immunization and Respiratory Diseases (NCIRD) at the Centers for Disease Control and Prevention (CDC). ID provides the scientific and programmatic foundation and leadership for the diagnosis, prevention, and control of influenza domestically and internationally.

The Domestic Surveillance Team of the Epidemiology and Prevention Branch in the Influenza Division at CDC collects, compiles and analyzes information on influenza activity year-round in the United States and produces FluView, a weekly influenza surveillance report, and FluView Interactive, which allows for more in-depth exploration of influenza surveillance data. The U.S. influenza surveillance system is a collaborative effort between CDC and its many partners in state, local, and territorial health departments, public health and clinical laboratories, vital statistics offices, healthcare providers, clinics, and emergency departments. Information in five categories is collected from eight different data sources. The applicant will be trained to support the coordination and management of at least one of the components of the U.S. influenza surveillance system.

Under the guidance of a mentor, the applicant will receive training regarding the coordination of national influenza surveillance activities including (1) the management, compilation, analysis, interpretation, and communication of weekly data, and (2) interacting with and providing guidance to state and select local public health personnel in regards to weekly reporting procedures, data cleaning/analysis and public health investigations. More specifically, the applicant will be trained in the use of SAS and Microsoft Access as well as systems specific to the surveillance component(s) and will assist with the creation of the weekly influenza surveillance report (FluView) and weekly PowerPoint slides. The applicant will also develop an understanding of the relationships between the Influenza Division and state and local public health agencies and how the groups work together to achieve common goals.

This program, administered by ORAU through its contract with the U.S. Department of Energy to manage the Oak Ridge Institute for Science and Education, was established through an interagency agreement between DOE and CDC. The initial appointment can be up to one year, but may be renewed upon recommendation of CDC contingent on the availability of funds. The participant will receive a monthly stipend commensurate with educational level and experience. Proof of health insurance is required for participation in this program. There are three full-time appointments available at CDC in the Atlanta, Georgia, area.  An appointment could begin as part-time and change to full-time if necessary.  Participants do not become employees of CDC, DOE or the program administrator, and there are no employment-related benefits.

Anticipated Appointment Start Date: April 1, 2019

Apply by clicking HERE


ORISE Fellowship National Youth Sports Strategy

Category : Alumni

The Office of Disease Prevention and Health Promotion within the U.S. Department of Health and Human Services has an opening for an ORISE Fellow in the Division of Prevention Science. The fellow will be involved with the development of a National Youth Sports Strategy. This division is involved with promoting the Physical Activity Guidelines for Americans and is currently developing the Dietary Guidelines for Americans. Ideal candidates have a master’s or PhD in physical activity, sport, exercise physiology/kinesiology, health, or a related field. Applications will be reviewed on a rolling basis. Questions can be directed to Katrina Piercy, PhD, RD, ACSM-CEP, katrina [dot] piercy [at] hhs [dot] gov.

Apply by clicking, HERE


BOOTS ORISE Fellowship

Category : Alumni

Data Management and Analysis Position

Description: The Office of Blood, Organ, and Other Tissue Safety (BOOTS), Division of Healthcare Quality Promotion (DHQP), National Center for Emerging Zoonotic and Infectious Diseases (NCEZID) is seeking qualified applicants for a an ORISE position starting summer of 2019.

The successful candidate will support 2 BOOTS-related activities: 1) the National Blood Collection and Utilization Survey (NBCUS) and 2) National Healthcare Safety Network Hemovigilance Module. Specific activities are described below.

NBCUS:

1) Participate in facility identification, outreach and enrollment for the NBCUS

2) Provide technical support to blood centers and healthcare facilities participating in the NBCUS.

NHSN:

1) Develop and maintain technical expertise in the function and use of the NHSN Biovigilance Component including thorough understanding of the application from a user perspective. This is a continuous activity.

2) Handle inquiries from existing and prospective NHSN Biovigilance Component users, assist facilities with NHSN enrollment, and provide user support regarding procedures for correctly applying CDC surveillance definitions and criteria and data entry. This is a continuous activity.

3) Participate in the change request and implementation process with the NHSN development team, including submitting change requests, defining business requirements with a business analyst, and testing and verification of the surveillance application prior to release. Changes to the surveillance system are released twice per year.

4) Investigating defects in the surveillance application as discovered by participating users, communicating defects to the NHSN QA team, verifying fixes, and communicating updates back to end users. This is a continuous activity.

5) Assist with data management, validation, and cleaning, including analyses to assess data quality and outreach to users for data entry correction and completion.

6) Identify and addresses opportunities to enhance usability of hemovigilance surveillance data for prevention.

7) Assist with the development of NHSN modules and mechanisms for electronic reporting to NHSN. Communicate with users and provides technical expertise to improve user interface and analytic and group user functions.

8) Assist with maintenance of the technical content of protocols, definitions, and data collection forms for the NHSN Biovigilance Component (including the hemovigilance module). Surveillance methods are reviewed at least annually

9) Attend weekly BOOTS staff meetings, bi-weekly NHSN User Support Team meetings, biweekly NHSN Development – User Support communication meetings, and weekly update meetings with technical monitor.

Requirements:

1) A Master’s degree and relevant experience in epidemiology and/or biostatistics.

2) Experience with SAS.

3) Experience with REDCap, Microsoft Access, and Microsoft Excel preferred.

4) Experience with data management and analysis preferred.

Interested candidates should send a CV and cover letter to Alexandra Savinkina at mxq1 [at] cdc [dot] gov.


Administrative Officer I, due 2/12

Category : Alumni

LOCATION OF POSITION

PHPA , Environmental Health Bureau, Center for Injury Epidemiology, Baltimore, MD

Main Purpose Of Job

The main purpose of this position is to serve as Coordinator of the CDC-funded Maryland Violent Death Reporting System (MVDRS), a statewide surveillance system that collects and reports detailed information on types of violent death in Maryland. This position leads the data abstraction activities and monitors data collection progress, engages with stakeholders to promote the use and dissemination of MVDRS data. In addition, the Coordinator serves as staff liaison to the advisory board.

MINIMUM QUALIFICATIONS

Education: Possession of a Bachelor’s degree from an accredited four-year college or university.

Experience: One (I) year experience in administrative or professional work.

Notes:

1. Candidates may substitute additional experience in administrative staff or professional work on a year-for-year basis for the required education.

2. Candidates may substitute additional graduate level education at an accredited college or university at the rate of 30 semester credit hours for each year of the required experience.

3. Candidates may substitute U.S. Armed Forces military service experience as a commissioned officer involving staff work that included regular use of independent judgment and analysis in applying and interpreting complex administrative plans, policies, rules or regulations or analysis of operational programs or procedures with recommendations for improvement on a year-for-year basis for the required education and experience.

DESIRED OR PREFERRED QUALIFICATIONS

The preferred candidate will have:

  • The ability to review and code medical examiner records, law enforcement records and abstract required information;
  • The ability to summarize and write concise narratives based on the information from the medical examiner and law enforcement records;
  • Experience entering complex data into web-based databases;
  • Experience with supervising staff or leading a program;
  • Experience with Microsoft Office or other data entry/management software;
  • Good organizational and multi-tasking skills;
  • Strong attention to detail;
  • Excellent oral and writing skills;
  • Experience in research and/or data entry (academic or professional); and
  • Experience or relevant course work in pathology or forensics.

SPECIAL NOTE: The Program Coordinator position duties require review of graphic materials related to violent deaths. 

For more information and to apply, click HERE


Research Data Analyst, UCSF

Category : Alumni

JOB OVERVIEW
The Research Data Analyst will join a collaborative and exciting team of researchers at the F.I. Proctor Foundation studying eye diseases in the U.S. and internationally. Researchers at the F.I. Proctor Foundation conduct randomized controlled trials and large epidemiological studies on ocular diseases that can cause blindness. The epidemiological studies involve large administrative databases and the trials involve domestic and international collaboration. This position requires an employee with excellent communication and organizational skills who can be relied upon to play an integral role in implementing and disseminating the results of research studies conducted at the F.I. Proctor Foundation.

The Research Data Analyst will provide research support through conducting literature reviews, assisting in data analysis and interpretation, writing, editing, and formatting manuscripts, and managing and tracking the progress of manuscripts for publications.

The Research Data Analyst must be comfortable working in a diverse team environment with little supervision to analyze, interpret, write, edit, review, and format manuscripts for high impact medical journals. Additionally, this position requires strong multitasking skills as the Research Data Analyst will also support the start-up of a National Institutes of Health (NIH)-funded multicenter, international clinical trial.

Responsibilities will include, but will not be limited to contributing to study design from a methodological standpoint, participating in the review and writing of protocols and study documents, assisting with database creation, helping to assure compliance with all relevant regulatory agencies, coordinating meetings with the study team, reporting study progress to investigators and other stakeholders, and generating subcontracts. This position will also involve travel to study sites for implementation and monitoring visits.

PROCTOR FOUNDATION FOR RESEARCH IN OPHTHALMOLOGY
The F.I. Proctor Foundation for Research in Ophthalmology at UCSF is committed to engaging in research activities and providing state-of-art patient care that address infectious and inflammatory disease that cause blindness. The mission is the prevention of blindness worldwide through research and teaching focused on infectious and inflammatory eye disease.

ABOUT UCSF
The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences, health professions and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences.

Required Qualifications

• BA/BS degree with a major in related field (e.g. biostatistics, public health, epidemiology) and two years of experience in project management or clinical research, or an equivalent combination of education and experience
• Knowledge of various study designs and implementation strategies
• Strong verbal and written communication skills
• Experience and ability to work and interact positively with people from diverse backgrounds
• Highly organized and able to multitask in a fast-paced environment
• Independence, planning, and decision making abilities to complete assigned duties

Preferred Qualifications

• Graduate degree in epidemiology, biostatistics, statistics, public health or related field and two to three years of relevant experience, or an equivalent combination of education and experience
• Demonstrated proficiency with statistical software packages (R, STATA or equivalent)
• Knowledge of database creation and management
• Understanding of HIPAA and Institutional Review Board (IRB) approval process
• Ability to develop budgets and track finances
• Experience in writing, editing, and reviewing scientific manuscripts
• Experience conducting literature reviews and writing scientific papers
• Experience in clinical research or demonstrated research or training experience that translates into a clinical research setting
• Knowledge of medical and scientific terminology
• Detail oriented; works with a high level of accuracy

To apply, click HERE.

Study Coordinator, UCSF

Category : Alumni

JOB OVERVIEW
The Study Coordinator will join a collaborative and exciting team of researchers at the F.I. Proctor Foundation studying eye diseases in the U.S. and internationally. Researchers at the F.I. Proctor Foundation conduct randomized controlled trials and large epidemiological studies on ocular diseases that can cause blindness. The epidemiological studies involve large administrative databases and the trials involve domestic and international collaboration. This position requires an employee with excellent communication and organizational skills who can be relied upon to play an integral role in implementing and disseminating the results of research studies conducted at the F.I. Proctor Foundation.

The Study Coordinator will support the start-up of a National Institutes of Health (NIH)-funded multicenter, international clinical trial. Responsibilities will include, but will not be limited to contributing to the study design from a methodological standpoint, participating in the review and writing of protocols and study documents, helping to assure compliance with all relevant regulatory agencies, coordinating meetings with the study team, reporting study progress to investigators and other stakeholders, maintaining finances, and generating subcontracts.

This position requires excellent professionalism as the Study Coordinator will be working with governmental and academic regulatory agencies, pharmaceutical companies, and researchers. This position will involve domestic and international travel to study sites for implementation and monitoring of visits. Additionally, the Study Coordinator should have strong writing and communication skill as this employee will be responsible for conducting literature reviews, writing, editing, and formatting manuscripts, and managing and tracking the progress of manuscripts to high-impact medical journals. The person in this position must be comfortable working in a diverse team environment with little supervision to carry out their responsibilities. The employee should show a strong interest in clinical research and a desire to contribute to the state of knowledge on the prevention, treatment, and correlates of disease.

PROCTOR FOUNDATION
The F.I. Proctor Foundation for Research in Ophthalmology at UCSF is committed to engaging in research activities and providing state-of-art patient care that address infectious and inflammatory disease that cause blindness. The mission is the prevention of blindness worldwide through research and teaching focused on infectious and inflammatory eye disease.

ABOUT UCSF
The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences.

Required Qualifications

• BA/BS degree with a major in related field (e.g. biostatistics, public health, epidemiology) and two years of experience in project management or clinical research, or an equivalent combination of education and experience
• Proficiency with computers, including ability to operate personal computer software (for example, Word, Access and Excel, email, electronic calendaring, Internet, et cetera) with sophisticated retrieval, storage, and merging capabilities
• Independence, planning and decision making abilities to complete assigned duties
• Time management skills and the flexibility to accommodate changing priorities in unit
• Strong organizational skills, the ability to multi-task, and work with frequent interruptions

Preferred Qualifications

• Graduate degree in epidemiology, biostatistics, statistics, public health or related field and two to three years of relevant experience, or an equivalent combination of education and experience
• Knowledge of relevant Federal and State regulations, and policies
• Excellent customer service skills, pleasant, helpful and patient
• Effective, efficient and tactful oral and written communication skills
• Ability to work in a team oriented setting, to prioritize work, and to follow through on routine assignments with minimal direction
• Ability to problem solve issues; listen, interpret and confirm understanding of others’ communications; and, to be objective
• Understanding of HIPAA and Institutional Review Board (IRB) approval process
• Ability to develop budgets and track finances
• Experience in writing, editing, and reviewing scientific manuscripts
• Experience conducting literature reviews and writing scientific papers
• Experience in clinical research or demonstrated research or training experience that translates into a clinical research setting
• Knowledge of medical and scientific terminology

To apply, click HERE


Epidemiologist, CDC Foundation

Category : Alumni

Description
The CDC Maternal Health Team and CDC Foundation have partnered to implement a project to increase U.S. capacity for collecting and using maternal mortality review data related to pregnancy-associated overdose deaths, in order to help develop a national picture of opportunities for eliminating these preventable maternal deaths. The project will provide support and resources to selected maternal mortality review committees, implement enhancements to the CDC developed Maternal Mortality Review Information Application (MMRIA), develop guidance for abstracting, reviewing, and using data on pregnancy-associated overdose deaths, and identify recommended approaches for prevention.
The Epidemiologist works closely with the Lead Epidemiologist, Project Manager, and the Senior Partnerships and Outreach Manager for the Building US Capacity to Review and Prevent Maternal Deaths Initiative to support project activities.
Responsibilities
• Analyze both qualitative and quantitative data from MMRIA
• Lead or co-lead qualitative and quantitative analysis webinars and in-person trainings.
• Provide distance-based and onsite technical support for selected maternal mortality review committees in analyzing and using qualitative and quantitative data collected on pregnancy-associated overdose deaths.
• Serve as lead writer and analyst on at least one publication.
• Serve as lead reviewer of toolkits or guidance documents related to informant interviews or focus group discussions.
• Contribute to additional reports and communication products from the project as needed.
• Build and manage partnerships with organizations to expand and support project work.
• Promote project at meetings and conferences as needed.

Qualifications
• A Master’s degree is required (preferably in Epidemiology, Anthropology, Psychology, or a related field); a Doctorate degree in one of the aforementioned fields is preferred
• At least two years of experience leading the analysis of both qualitative and quantitative data
• Proven ability to publish in peer-reviewed journals and present findings at conferences
• Proficient in at least one statistical analysis software program; SAS is preferred
• Proficient in at least one qualitative analysis software program; MaxQDA is preferred
• Facilitation and conflict management skills; flexible and adaptable
• Detail-oriented with strong organizational skills
• Able to work independently and within a team environment
• Strong communication skills, both written and oral

For more information and to apply, click HERE.


University of Massachusetts Accepting PhD Applications

Category : Alumni

PhD program still accepting applications: The University of Massachusetts Medical School Department of Population and Quantitative Health Sciences is still accepting applications for doctoral training in clinical and population health research (deadline: March 1, 2019). This post-master’s program offers competitive stipends ($31,850 + health insurance and tuition and fees), a curriculum individualized to each student’s research interest, and full immersion into the research enterprise from day 1 in the program. See the brochure for more details and feel free to contact Kate [dot] Lapane [at] umassmed [dot] edu for further information.


Oxfam, Data and Information Analyst

Category : Alumni GLEPI

Oxfam International has been refining and improving processes related to annual planning (programs and resources), program quality reflection, operational progress and budget reporting, and program results reporting. These processes and formats generate quantitative and qualitative data, as well as information on Oxfam programs and resources.

The data and information are to be collated, aggregated, analyzed, visualized/displayed, and used in decisionmaking and governance processes. Some of the analyses are routine and pre-defined by Oxfam’s annual and quarterly management and reporting processes; others are ad-hoc, one-time, and/or tailored to specific questions and needs. Quantitative analyses require descriptive and some inferential work, as well as data visualization. Analyses may be both inductive and deductive, depending on purpose and questions raised. It may be necessary to set up syntax, in appropriate statistical software, to import, merge and analyze data and provide visualization on a routine basis with new data collected annually. Products will range from PowerPoints summarizing findings, to brief written narrative pieces, to Excel sheets with aggregated data, to infographics visualization pieces. When analyses are written up in narrative form, they should be suitable for brief, user-friendly, wide-consumption pieces such as Workplace posts, blog posts, podcasts, etc.

Examples of existing processes that need data analysis

1. Evaluation reports

2. Planning and reporting exercises from different groups, from which we need to extract topline summaries

3. Questionnaires (e.g. customer satisfaction; consultations, systems for mutual accountability and stakeholder feedback)

4. Analysis and sense-making of progress reports

5. Output reports (quantitative and qualitative data)

Approach

The clients of analyses, and main consumers of the analyst’s work, are mainly management and governance staff, such as regional directors, country directors, regional leadership teams, global program director, knowledge for impact director and team, operations director and team, governance bodies. The approach of the analyst will entail:

• working with clients to understand and help define/sharpen their questions based on their purpose and needs;

• preparing datasets as needed (e.g., by importing, or merging, or extracting, etc.);

• conducting analyses;

• preparing and sharing the output in an appropriate and user-friendly format;

• discussing and validating it with clients;

• advising, in an iterative process as appropriate, on what questions the data, information and analyses can and cannot answer;

• refining, adding, or adjusting as necessary based on client inputs and requests; and

• finalizing the analysis products to be used internally and externally

In this, the analyst will take a strong customer-focused approach and maintain customer satisfaction as a key measure of success. At the same time, the analyst will maintain the appropriate level of rigor in handling, managing, and analysing all data and information. While not setting the agenda for analyses or defining the purpose and questions, the analyst will be expected to liaise with various Oxfam teams and departments to understand the work well enough – particularly the larger processes that produce the data and information – to perform analyses and advise on them in ways that are appropriate and fit-for-purpose.

In addition, the analyst will collaborate with Oxfam Affiliates to bring together datasets for cross-confederation use and analysis. These may be data expressly collected for monitoring, evaluation, and/or research purposes, or data generated in the course of Oxfam performing its work, such as data in various management systems and reports. In either case, the work will require designing the merge and resulting new dataset, and working with colleagues in Oxfam Affiliates to carry out the

Skills

• Quantitative, qualitative, and mixed methods analysis

• Statistical software (with preference for open-source solutions)

• Qualitative analysis software a plus • Strong customer focus

• Ability to balance rigor with creative approaches to arrive at fit-for-purpose products

• A sense of humour and a dose of patience

• Problem-solving attitude and track record

• Strong interpersonal skills

• Ability to communicate analyses to management without jargon, in a succinct, easy to digest manner

• Cross-cultural communication or experience in cross-cultural/international settings a plus

• Experience working virtually and remotely

• Willingness to work outside of usual office hours to accommodate different time zones

• Ability to plan work, self-direct, and meet short deadlines

• Fluent in both oral and written English. Working knowledge of Spanish and/or French is desirable.

Conditions:

This is offered as a consultancy for 12 months, from late January/early February 2019, on a full-time basis (approximately 35 hours per week). Why a short-term assignment? This is a new function that we need to test and learn. Eventually adapt or develop into a longer-term position in the program teams. The position will be reporting to the Knowledge for Impact Team (KIT) of Oxfam, with a % of the time dedicated to joint work between KIT and Operations, mainly the planning 2019-20 and the reporting 2018-19 cycles.

Location: home-based or one of the Oxfam offices.

Remuneration: to be discussed

Contact: Velina Petrova (Velina [dot] petrova [at] oxfam [dot] org) and Cristina Sette (Cristina [dot] sette [at] oxfam [dot] org)


Upcoming Events

  • Humphrey Fellows Noontime Seminar Series April 25, 2024 at 12:00 pm – 1:00 pm Networking and Guest Lecture and Meeting and Special Event and Student Event; zoom.us… Online Location: https://zoom.us/j/95325531576Event Type: Networking,Guest Lecture,Meeting,Special Event,Student EventSeries: Noontime SeminarSpeaker: Various Speakers - see details by dateContact Name: Kris ValerianoContact Email: kvaleri@emory.eduRoom Location: RRR_R809Link: https://sph.emory.edu/departments/gh/fellows/humphrey-fellows/index.htmlFellows will present on a topic pertaining to their home country, culture and/or their work in public health.Deb Mcfarland Room, 8th floor RRR.3.28: Abeselom Gutta, MD &Yeshoda Aryal, MPH4.11: Ola Ziara,…
  • Tips from the Other Side of the Peer-Review Process to Help Get Your Scientific Manuscript Published April 25, 2024 at 12:00 pm – 1:00 pm Guest Lecture Event Type: Guest LectureSeries: Center for Faculty Development and ExcellenceSpeaker: Bruce G. Weniger, Adj Assoc Prof, RSPHContact Name: Carol ColaninnoContact Email: ccolani@emory.eduLink: https://forms.gle/uhaExcRPKar39LuC7Examples good and bad, templates, andanecdotes from journal-editor experience tolimit the burden and skepticism of busyreviewers who use conscious criteria andsubjective, often unconscious intuition to judgepublication worthiness using only yourmanuscript and revision cover…
  • 2024 Charles C. Shepard Award Symposium May 8, 2024 at 12:00 pm – 1:15 pm zoom.us… Online Location: https://zoom.us/j/96537866614The Charles C. Shepard Award is given to thegraduating masters student who is deemed bythe faculty to have prepared the most scholarlyresearch paper. Please join us to recognize andcelebrate this year’s finalists who will present aposter of their work.

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