‘Career Options: Regulatory Affairs’
PhD Career Stories: The Evolution of Purpose: A Scientist’s Journey from Basic Research to Scientific & Regulatory Affairs to Product Design & Development at Mars, an International Food Company
Mar. 29, 2024— Registration Requested Jacob Brown, Ph.D. Product Development Scientist, Mars PetCare Dr. Brown received his BS and MS in Physiology and Developmental Biology from Brigham Young University. He received his Ph.D. in Physiology from the University of Missouri- Columbia. He completed his postdoctoral fellowship at Vanderbilt University in 2019. He started his tenure...
Upcoming Webinar: Postdoctoral Opportunity at NIH & FDA: The Translational Science Interagency Fellowship
Oct. 18, 2023—The Translational Interagency Fellowship (TSIF) program is jointly sponsored by NCATS and the U.S. Food and Drug Administration (FDA) and aims to provide training in both translational science and regulatory science. Fellows will be trained in preclinical translational science, technology development, and regulatory science and review. “By combining training in translational science and research-related regulatory...
Lilly Visiting Scientist Fellowship Program applications open
Sep. 14, 2022—The Lilly Visiting Scientist Fellowship is a unique one-year, post-graduate program for Pharm.D., M.D., and relevant Ph.D. or master’s degree graduates. The program exposes fellows to a myriad of pharmaceutical functions and provides hands-on involvement with the drug development process. Fellows are assigned to one department yet work closely with other areas, enabling them to...
Regulatory Writer Acceleration Residency, (remote) Certara Synchrogenix, applications opening late fall
Jun. 8, 2022—Regulatory Writer Acceleration Residency : Developing the Next Generation of Regulatory Writers Come Grow with Us! Regulatory Writer Acceleration Residency (RWA Residency) is a unique opportunity for those interested in becoming a regulatory writer. Learn from a team with a proven track record of success in various disciplines of regulatory writing. We invite you to join...
Synchrogenix Regulatory Writer Acceleration Residency
Sep. 23, 2021—Synchrogenix is accepting applications for the 2022 Regulatory Writer Acceleration Residency (RWA Residency). The Residency is a unique opportunity for those interested in becoming a regulatory writer to learn from a team with a proven track record of success in various disciplines of regulatory writing. Residents will embark on a two-year curriculum and have the...
Janssen Scholars of Oncology Diversity Engagement Program: Call for Applications
Jun. 24, 2021—Janssen recently announced the launch of the Scholars of Oncology Diversity Engagement Program (SODEP), which will begin in fall 2021. SODEP consists of three steps: 1. Exposure to industry at the virtual Janssen Oncology Day, an all-day program that will provide an overview of the various opportunities within science and medicine. 2. One-on-one mentorship. Up to 10 scholars who...
Employer Info Session: Poly-Med
Jun. 10, 2021—Join us for an Employer Information Session with Poly-Med on June 24, 11:30am, via Zoom. Co-sponsored by the BRET Office of Career Development ASPIRE Program and the Vanderbilt Career Center. Register via Zoom. Poly-Med is the leading developer of bioresorbable polymers and fibers. We help innovative medical device companies focused on improving patient outcomes. Poly-Med...
2021 ASPIRE Career Symposium: Managing Panel
Apr. 7, 2021—It’s time for the 2021 ASPIRE Annual Career Symposium: Careers for the Citizen Scientist! MANAGING PANEL Friday, May 7 1:30-2:30pm CST Zoom Webinar Register for Managing Panel Dr. Zusi Andrews, PhD, Biologist and Medical Writer, NIH/NCI Dr. Zusi Andrews, PhD, is a trained biologist and medical writer for the NIH (NCI). As a medical writer and science...
November PhD Career Stories: Patricia Costa-Giomi, PhD
Oct. 22, 2020—For November’s ASPIRE PhD Career Stories session we are featuring Patricia Costa-Giomi, PhD Executive Director International Regulatory Affairs at Ultragenyx Pharmaceuticals This session will be offered via Zoom. Be sure to register in order to receive the Zoom login information Registration required Patricia Costa Giomi received her PhD in Biochemistry from University of Buenos Aires,...
Skills and Exploration Workshop: Regulatory Affairs
Sep. 29, 2020—The BRET Office of Career Development ASPIRE Program is excited to welcome regulatory expert Linda Bowen, RAC, FRAPS, to facilitate a small virtual regulatory-intensive workshop. All details below: Transitioning to a Career in Regulatory Affairs and FDA Overview Virtual Workshop December 10, 11, 17, and 18 2-5 PM (central time) Linda Bowen has over 35...
Informational Webinar Series about Lilly Visiting Scientist Fellowship Program
Sep. 4, 2020—Lilly’s Visiting Scientist Fellowship program exposes Pharm.D., M.D. and relevant Ph.D. or master’s degree graduates to a myriad of pharmaceutical functions and experiences, providing hands-on involvement with the drug development process. The fellowship is a unique one-year, post-graduate program. Fellows are assigned to one department, yet work closely with other areas, enabling them to learn...
Medpace Recruiting Event in Nashville
Feb. 14, 2020—Interested in clinical research and/or regulatory affairs or medical writing? A clinical research organization called Medpace in Cincinnati, OH will be in Nashville, hosting a recruiting next Wednesday, February 19. The company has quite a few openings they are trying to hire for in regulatory affairs, medical communication, and clinical trials and the recruiting event...
Avalere’s FDA Fellowship Program
Aug. 23, 2019—Avalere’s FDA Fellowship Program invites applications from advanced degreed professionals, who have strong backgrounds in science and technology and are looking to transition their scientific background into the science/health policy and business environments. The Fellowship Program is small and highly selective. As an FDA Fellow, participants will spend 6 months immersed in health and life...
Job Opportunity: Clinical Research Regulatory Specialist II, Johns Hopkins University, Baltimore, Maryland
Aug. 22, 2019—Regulatory Specialist II The Department of Oncology is seeking a Clinical Research Regulatory Specialist II that will serve as a central resource for faculty conducting clinical research at Johns Hopkins University and across multiple clinical trial sites. Working closely with the Sponsor-Investigator and IND Specialist, this position will assist in the submission of investigator initiated...
Transitioning to a Career in Regulatory Affairs: a Two-Day Campus Workshop
Jan. 17, 2019—The BRET Office of Career Development is excited to welcome Linda Bowen, a senior regulatory policy and intelligence leader and speaker, to lead the special opportunity: Transitioning to a Career in Regulatory Affairs The workshop will be held on Friday, March 8 AND Saturday, March 9, both days from 8:00am to 4:00pm, in Light Hall....
Job Opportunity: Avalere Health FDA & Regulatory Fellow, Washington, DC
Dec. 14, 2018—FDA Fellowship Program Avalere’s FDA Fellowship Program invites applications from advanced-degree professionals who have strong backgrounds in science and technology and are looking to transition their scientific background into the policy environment. Small and highly selective, our FDA Fellows spend 6 months immersed in healthcare regulatory policy and strategy issues. In this full-time, paid fellowship,...
Regulatory Affairs Fellowship Program at Johns Hopkins, Baltimore Maryland
Sep. 10, 2018—Regulatory Affairs Fellowship Program at Johns Hopkins The Professional Development and Career Office at Johns Hopkins University School of Medicine has invited the BRET Office of Career Development to nominate a Vanderbilt biomedical trainee to attend this all expenses-paid workshop supported by a 2017 Career Guidance Award from the Burroughs Wellcome Foundation. It will take place at...
PhRMA Foundation Fellowship Opportunity: Regulatory Science Fellowship (Deadline: April 1)
Feb. 12, 2018—Regulatory Science Fellowship (Deadline: April 1, 2018) Regulatory Science Fellowships provide a $70,000 stipend for a year of on-site professional experience. Fellows are provided a full year of on-site industry experience, working within a global pharmaceutical company’s regulatory affairs department. Fellows will work closely with the regulatory science team, where they will participate in...
Job Opportunity: Risk Assessment Specialist – Chemicals, The Leyden Group
Sep. 25, 2017—The person sought for this position will work in a group of expert regulatory and product safety professionals within a Department of Regulatory Affairs and Product Stewardship. Our client company is a large and diverse, specialty chemical company located in the Southern U.S. With the emergence of regulations requiring exposure and risk characterization, the company...