Conferences & Symposia
Addiction Research Symposium Plus

Interested in addiction research? Want to meet collaborators and develop grant proposals?

Join Tufts CTSI for our Addiction Research Symposium Plus on Wednesday, March 13 at Tufts University’s Boston Health Sciences Campus. This interactive event will focus on nascent research projects with the goals of assisting teams to develop research project proposals for future grant submissions and engaging all event participants in team science approaches to further catalyze research ideas.

By the end of this interactive symposium, event participants should be able to:

  • Identify common regulatory concerns surrounding the unique populations involved in addiction research.
  • Recognize how research teams develop research projects, from concept toward a written funding proposal.
  • Identify Tufts CTSI team-based translational science resources that can help advance a research project.
  • Articulate the value of gathering peer and expert feedback during the development of fundable proposal.

Selected Proposals

The following projects will be presented and discussed:

  • Oxygenating the Addicted Brain Through Aerobic Exercise, Eduardo Fontes, PhD, Federal University of Rio Grande do Norte and Tufts University School of Arts and Sciences
  • Incorporating Acupuncture into the Continuum of Care for People with Severe Opioid Use Disorder, Barbara Herbert, MD, Column Health and Tufts University School of Medicine
  • Intranasal Glial-Derived Neurotrophic Factor (GDNF) Gene Therapy for Opioid Use Disorder, Barbara Waszczak, PhD, Northeastern University Bouve College of Health Sciences; Emmanuel Pothos, PhD, Tufts University School of Medicine
  • Salivary Gene Analysis and Brain MRI to Understand Hypothalamic and Reward Pathway Dysregulation Affecting Oral Feeding in Infants with Neonatal Opioid Withdrawal Syndrome, Elizabeth Yen, MD; Jill Maron, MD, and Jonathan Davis, MD, Tufts Medical Center Pediatrics Department

Details

Wednesday, March 13, 9:00AM-3:00PM
Graduate School of Biomedical Sciences, Room 216A
145 Harrison Avenue, Boston MA

Registration

To attend, please register here by March 4, 2019.

Seminars & Workshops
Clinical Research Staff Quarterly Training: July 2021

The July 2021 Clinical Research Staff Quarterly Training will focus on hot topics in IRB and research compliance.

Big changes are coming to IRB forms and submission processes. Join us on July 15 for the next session of the Tufts Medical Center (Tufts MC) and Tufts CTSI Professional Education Clinical Research Staff Quarterly Training series. You’ll get the inside scoop on what is new, what you will be required to do, and best practices for working with the Tufts IRB. If you are involved in study start-up activities or interact with research participants or IRB submissions, these sessions are for you! These quarterly trainings are also a great way to get connected to the community of clinical research professionals at Tufts MC.

The July session continues our focus on topics in research compliance specific to Tufts MC. Whether you are an experienced coordinator, or new to Tufts MC, there will be something here that is relevant to your work.

Featured Speakers

Christine Choy, IRB Supervisor and Database Administrator

Caitlin Farley, IRB Administrator II

Carly Tucker, Clinical Research Compliance Manager

Featured Topics

Diversity Enrollment, Biospecimen Banking, and More

The IRB office recently updated their forms and templates to reflect new processes to highlight and improve enrollment of diverse populations, their updated Biospecimen banking (formerly tissue banking) policy, and much more. You will learn about all of these changes; which forms, templates, and policies were revised, created, and eliminated; and how these changes will affect current and new studies.

Best Practices for IRB Submissions and Responding to IRB Comments

The IRB office will provide tips and guidance for a smooth and efficient IRB review of your projects. You will learn best practices for submitting studies to the Tufts IRB, responding to comments and requested revisions, and getting your study approved as quickly as possible.

Third Party Vendor Risk Assessment Update

This short update will cover the EVA page for approved research vendors including: where to find the list, how to best understand and use the approved vendors list, and other tips and tricks for this new vendor review.

Who should attend

Clinical research staff are encouraged to attend.

Details

Thursday, July 15
1:00-2:00PM
Online via Zoom (a link will be sent to those who register).

Registration

To attend, please register here.

 

 

Seminars & Workshops
Clinical Research Staff Quarterly Training: May 2021

The May Clinical Research Staff Quarterly Training will focus on hot topics in research compliance.

Tufts Medical Center and Tufts CTSI Professional Education are excited to announce the re-launch of the Clinical Research Staff Quarterly Training series. The first training in the new series will focus on topics in research compliance specific to Tufts Medical Center.

Featured Topics

Clinical Research Pre-Registration

The Clinical Research Pre-Registration (Pre-Reg) form is used for patients coming into the hospital for inpatient or outpatient study visits that are scheduled for ancillary care. You will learn how to complete a Clinical Research Pre-Registration form and the importance of this information as it relates to research billing compliance.

Greenphire Clincard

Greenphire Clincard system is the preferred method for providing compensation or reimbursement to subjects in clinical research studies. We will discuss how to get studies added to Clincard, why the system is the most compliant way to pay research subjects, FAQs around using the system and important things to consider when requesting an alternative method.

Research Third Party Vendor Onboarding and Risk Assessment

Wellforce has recently rolled out a new Third Party Risk Management (TPRM) process including a new TPRM Vendor Onboarding Form. We will discuss when this form should be completed as part of study start-up and how to best complete it as it relates to research.

Who should attend

Clinical research staff are encouraged to attend.

Details

Friday, May 7
1:00-2:00PM
Online via Zoom (a link will be sent to those who register).

Registration

To attend, please register here.

 

 

Seminars & Workshops
Demystifying Cancer Clinical Trials

Want to learn about, or conduct, cancer clinical trials?

Tufts CTSI and the Cancer Center at Tufts Medical Center are hosting a free 20-hour course for fellows, faculty, research team members, and anyone interested in the process of conducting cancer-related clinical trials.

Documents

Session 1, October 14, 2016
Session 2, November 18, 2016
Session 3, December 16, 2016

Session 4, February 10, 2017

Session 5, March 24, 2017

 

Details

Demystifying Cancer Clinical Trials will take place on Fridays, from 1:00-5:00PM on the Tufts Health Sciences Campus in Boston:

  • October 14 (35 Kneeland Street, 8th Floor, Boston)
  • November 18 (Tufts University Center for Medical Education, Room 114, 145 Harrison Avenue, Boston)
  • December 16 (35 Kneeland Street, 8th Floor, Boston)
  • February 10 (35 Kneeland Street, 8th Floor, Boston)
  • March 24 (35 Kneeland Street, 8th Floor, Boston)

Course sessions will also be videorecorded and posted on Tufts CTSI’s I LEARN website.

Attendees are encouraged to review other courses on I LEARN prior to the start of Demystifying Cancer Clinical Trials.

Goals

At the conclusion of the course, participants will be able to:

  • Explain how to navigate investigator-initiated clinical trial processes in cancer.
  • Discuss how to work with pharmaceutical industries and other for-profit entities.
  • Define investigational new drug (IND) and investigational device exemption (IDE) studies and explain how IND/IDE clinical trials are conducted.
  • State the Principal Investigator’s responsibilities for leading a clinical trial as well as the responsibilities of the research team.

To Register

To attend, sign up here. Participants are encouraged to attend all five sessions.

 

 

Seminars & Workshops
Pediatric Clinical Trials Workshop

Seminar Info

Need a larger sample size for your clinical trial? Interested in increasing research participation from children with diverse backgrounds? Join Tufts CTSI and Children’s National CTSA on Wednesday, April 18, 2018, 8:00AM-5:00PM in Washington DC, Marriott Wardman Park, at an inaugural workshop, Challenges & Opportunities in Pediatric Clinical Trials, designed for pediatric investigators and their teams.

This free, one-day, immersive case-based workshop is the first CTSA hub-sponsored forum for all levels of investigators to reflect on the core competencies expected for today’s pediatric clinical studies. It will take place the day before the Association for Clinical and Translational Science’s Translational Science 2018.

Details

Wednesday, April 18, 8:00AM-5:00PM
Washington Marriott Wardman Park, Washington, DC, Madison Room
(*prior to ACTS Annual Meeting 4/19/18–4/21/18)

Seminars & Workshops
Pfizer Investigator Training Program (iTP)

Acclaimed training program begins April 18, 2017

Tufts CTSI will host Pfizer’s acclaimed Investigator Training Program (iTP) on April 18-19, 2017.

This unique, two-day, free-of-charge program will empower clinicians to build critical skills required for the recruitment, management, conduct, and reporting of clinical trials. It will examine the entire trial process, from planning stages to trial close-out activities, and will provide practical recommendations for increasing the efficiency of clinical trial conduct at investigative sites.

Led by clinical trial experts, this interactive training will consist of didactic lectures, discussions, and group activities. The iTP is targeted to investigators and the entire clinical study team, including research fellows, coordinators, research nurses, data managers, regulatory, and IRB members. Clinical trial experience (even if limited) is encouraged, though not required.

Attendees will receive a certificate of attendance after completing this International Conference on Harmonisation (ICH)/Good Clinical Practice (GCP) program. This workshop is approved for 16.5 contact hours towards maintaining an Association of Clinical Research Professionals (ACRP) certification. Contact hours are applicable to CCRCs, CCRAs and CPIs at an entry-level knowledge base.

This is a popular training, and class size is limited, so please pre-register by no later than April 7. You will receive an official email invitation from Pfizer if you are admitted to the program.

Please note: registration is a two-step process. Once you pre-register with Tufts CTSI, you will receive a formal registration form from Pfizer. You must be registered with Pfizer in order to attend this training and receive certification.

Details

Tuesday, April 18, 7:30AM-5:00PM
Wednesday, April 19, 8:30AM-3:30PM
Registration and continental breakfast begin at 8:00AM.

Tufts Center for Medical Education, Room 114
145 Harrison Avenue, Boston MA

Contact

Questions? Please email info@tuftsctsi.org for assistance.