Cambridge University Press & Assessment About us. A Junior Research Fellowship is a postdoctoral position tenable for up to 4 years. This Fellowship does not, therefore, require a doctorate to be obtained before taking up the position. Research Fellowships are held on condition of residence within the University of Cambridge. All Rights Reserved. Royal Society schemes, in particular the University . Junior Research Fellows. This cookie is set by the provider Dotmetrics.net. Applications must be submitted on-line via the Christs College website at www.christs.cam.ac.uk/jrf by 12:00 noon on Thursday 20th October 2022. 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There is no age limit, but a Fellowship is intended to support those at an early stage in their academic careers, who will expect, in due course, to go on to hold posts in educational institutions of international standing. Liane Kuo, Pharm.D., is the 202022 St. Johns University/Daiichi Sankyo Pharmaceutical Industry Fellow in Clinical Development/Oncology. Facebook. Application Process for fellowships beginning on or about July 1, 2024: Information pertaining to Fall 2023 fellowship webinars and application deadlines will be posted to this website late summer/early fall 2023. Full-time + 1. Dr. Huynh earned her Doctor of Pharmacy degree from Philadelphia College of Pharmacy (PCP). She is excited to join the St. Johns and Pfizer Inc. fellowship team and feels fortunate to work in a role that aligns all her interests. During this unique two-year fellowship, the fellow will use her/his skills to make positive impact on global patient care. The closing date for applications is Monday 17th January 2022 at noon. 50 Goddard Avenue, Brookline, MA 02445 | Tel. To be eligible, candidates must graduate from an Accreditation Council for Pharmacy Education (ACPE) accredited Doctor of Pharmacy program and have a keen interest in pursuing a career in the pharmaceutical industry. The Fellowship is open to graduates of any University who are engaged in research in any aspect of the Sciences. If you are shortlisted, you will be required to submit a complete or nearcomplete dissertation. Whatever your circumstances, if you have what it takes to make the most of life at St John's, we want to hear from you. Candidates will usually have completed their PhD, but must not have undertaken more than 2 years of postdoctoral work by 1st October 2020 (i.e. The Fellowship Administrator Churchill College Storey's Way Cambridge CB3 0DS. In her free time, Dr.Thompson enjoys yoga, reading, and trying new eateries (she is passionate about al fresco dining). She was an active member of the student chapters of theAmerican Pharmacists AssociationandIndustry Pharmacists Organization. The fellowship spans a variety of payer archetypes and involves establishing strong working relationship with market access, HEOR, commercial, medical and clinical develop functions. These two-year post-doctoral pharmaceutical industry fellowships are designed to provide the Doctor of Pharmacy graduate a profound and unique experience within a pharmaceutical corporation, Myovant Sciences. In her free time, Dr.Thompson enjoys yoga, reading, and trying new eateries (she is passionate about al fresco dining). The administration of the Scheme is conducted by the Fellowship Administrator at Churchill College. 1137497, 2023 Homerton College It is also possible, subject to the approval of the Council, to postpone or interrupt enjoyment of the stipend and privileges of a Fellow. It is the goal of the program to provide the fellow with the skills and tools necessary for a successfulcareer in the pharmaceutical industry. Associate Professor of Medieval and Eurasian . Theme: Newsup by Themeansar. . Fellowship Goals and Objectives for Early Clinical Development: Fellowship Goals and Objectives for Clinical Regulatory Affairs, Fellowship Goals and Objectives for Commercial Regulatory Affairs. The overall objective for the fellowship is to provide hands-on experience in either Early Clinical Development, Clinical Regulatory Affairs, or Commercial Regulatory Affairs, with exposure to other functional areas during the program. Emeritus Fellows often remain active in research. Dr. Villariasa earned her Doctor of Pharmacy degree from St. Johns University in 2022. 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Si Li, Pharm.D., is the 202022 St. Johns University/Pfizer Inc. Pharmaceutical Industry Fellow in Oncology Global Market Access and Health Economics and Outcomes Research (HEOR). . Dhiviya Samuel, Pharm.D. Home. Dr. Beebe loves to play, watch, and talk about sports. Academics & admissions Research and Junior Research Fellowships Research and Junior Research Fellowships We offer a variety of ways through which post-doctoral researchers and others can become members of our community either as a Junior Research Fellow (JRF) or Research Fellow (RF). Those studying for a PhD outside the UK might wish, if necessary, to apply for a deferral in order to complete their studies. Stay informed with our Daily Blog Digest and MJC News updates. She will work on bringing to market a novel therapeutic option for patients living with major depressive disorder. [SEE FULL LIST] St John's College is a constituent college of the University of Cambridge (the full, formal name of the college is The Master, Fellows and Scholars of the College of St John the Evangelist in the University of Cambridge). Following her rotations at BioCentric, Inc. and the US Food and Drug Administration, Dr. Nghiem was committed to pursuing a career in the pharmaceutical industry. The College wishes to encourage applications from a wide range of candidates and the Fellowships are available in all branches of University studies. The College runs an annual Research Fellowship Competition. Follow us. The objective for the fellowship is to provide hands-on experience in advanced techniques pertaining to HEOR evaluation of cancer pharmaceuticals, in addition to market access experience, to introduce and develop valuable skills in an increasingly important discipline. Eligible candidates are elected to Research Fellowships at Trinity on the basis of the quality of the research they submit, and the evidence that it provides of high originality and promise. Diverse, driven, and dynamicSt. Archives. fellowship programs designed to train the Doctor of Pharmacy graduate in specific practice areas of the pharmaceutical industry. Director of Studies at St John's College. A Research Fellowship provides an opportunity to spend up to four years in Cambridge undertaking postdoctoral research or scholarly work at an early stage of an academic career. In particular, the standard of research expected for election to a Fellowship is much higher than that which is merely adequate for a good PhD. Making an Impact. The St. John's University College of Pharmacy and Health Sciences offers two-year, post-Pharm.D. The two-year post-doctoral pharmaceutical industry fellowship is designed to provide the Doctor of Pharmacy graduate a profound and unique experience within a pharmaceutical corporation, Pfizer. These cookies help provide information on metrics the number of visitors, bounce rate, traffic source, etc. Dr. Thompson has also been involved in several research projects and was recently given the Geriatrics and Gerontology Education and Research Program Award in recognition of her contributions to the field of geriatric pharmacy. I'm an MD student at the American University of Antigua learning the nuances of clinical practice. Richard Partington, currently Senior Tutor and Fellow of Churchill College, Cambridge, will join St John's in August, and formally takes up his new role as Senior Tutor from 1 September 2021. For example, I am co-investigator on a project developing and . The Fellows and students at Newnham carry out world-class research across a wide range of disciplines. She earned her Bachelor of Science degree in Biochemistry from Western Kentucky University, and her Doctor of Pharmacy degree from the University of Maryland, Baltimore, MD. She also served as President of the IPhO chapter, and additionally as a IPhO National Student Officer. Dr. Samuel is excited to be the inaugural fellow for this new and exciting St. Johns University/Relmada Therapeutics, Inc. fellowship opportunity, and work with a team focused on addressing diseases of the central nervous system. Formal and informal educational opportunities, Collaborative research projects with St. John's University faculty, Development of continuing education courses, A resident and fellow seminar series in collaboration with the College of Pharmacy and Health Sciences, Graduate degree programs available at the university to further his or her educational development (Master's or PhD degrees), On-campus teaching opportunities within the Doctor of Pharmacy Program, Opportunity to participate in a Teaching Certificate Program, Develop and utilize strong clinical trial analysis skills to evaluate medical literature, interpret scientific data, and support healthcare professionals and consumers, Create and present educational lectures on products and disease states to internal and external stakeholders, Attend medical/scientific meetings to ensure an in-depth understanding of the latest advances and updated scientific information that will help shape our publication and Investigator Sponsored Study strategies, Work with the Medical Affairs team including, but not limited to: Medical Communications Leads, Medical Science Liaisons, Medical Directors, Medical Writers, and other relevant team members on the development and approval of core clinical material, Manage company expectations while effectively integrating key clinical messages for dissemination to a wide array of audiences, Acquire the medical expertise and experience to thrive in the pharmaceutical industry while complying with FDA and PhRMA regulations, Establish and maintain working relationships with healthcare professionals, Provide education by creating scientific dialogue around American Regent products and sponsored research, Fellows will have the opportunity to shadow the Medical Science Liaison (MSL) team and attend relevant conferences to deepen their understanding of Medical Affairs in a professional, pharmaceutical industry setting, Collaborative research projects with St. Johns University faculty, Graduate degree programs available at the university to further his or her educational development (Masters or PhD degrees), Provide clinical pharmacology and scientific input into early clinical development plans, Contribute to the preparation of early clinical development components of regulatory documents, including Investigational New Drug Applications (INDs), Investigational Medicinal Product Dossiers (IMPDs), Clinical Trial Applications (CTAs), and submission documents, Provide scientific input into the rationale, study design, and study assessments/procedures for early clinical development studies, including coordination with pharmacometrics, bioanalytics, and biostatistics, Collaborate with the early clinical development operations team to support development of clinical study protocols and study-related activities during the initiation, execution, and close-out of early clinical development studies, Collaborate with cross-functional study teams to provide oversight and management of early clinical development studies, Contribute to the interpretation of clinical, pharmacokinetic, pharmacodynamic, and safety data from early clinical development studies, including co-authoring and review of clinical study reports, Support early development teams (EDTs) by participation in team and subteam meetings, including preparation of scientific content relevant to strategic decision-making, Develop a comprehensive understanding of global regulations, guidances related to drug development, and the regulatory environment, Support cross-functional product teams by offering strategic guidance on regulatory requirements and design a regulatory strategy for development and market registrations, Ensure Investigational New Drug Applications (INDs), New Drug Applications (NDAs), Marketing Authorization Applications (MAAs), and Clinical Trial Authorizations (CTAs) are maintained in compliance with local regulatory requirements, Interact with internal and external stakeholders to ensure company compliance with all appropriate federal regulations and guidances, Develop a thorough understanding on how to best conduct health authority meetings and prepare teams for effective regulatory interactions, Provide Myovants internal stakeholders with strategic regulatory advice on advertising and promotional materials, in accordance with FDA regulations and business goals, Gain insight into marketings goals and objectives and understand how those measures are reflected in the development of product advertising, Develop a comprehensive understanding of FDA regulations regarding drug advertising and promotion, Apply regulations to the development of product promotion (including, but not limited to, television commercials, social media advertisements, website design, and print brochures), Build and maintain expertise in payer regulations and priorities across major countries, Partner with an asset market access lead to execute the market access and pricing strategy for the assigned oncology asset, which includes but is not limited to, executing payer market research, developing payer value proposition and story, market access and pricing negotiations, payer benefit analysis, and contracting solutions, Gain proficiency in the field of health economics, outcomes research, and comparative effectiveness research (CER), In collaboration with global HEOR leads, conduct outcomes research evaluations with real world data, develop health economics models to characterize and communicate product budget impact and cost-effectiveness; participate in HEOR projects and gain experience in how a pharmaceutical manufacturer uses clinical, economic and humanistic data to support the development and commercialization of its products, Lead the timely development of United States HEOR launch excellence deliverables including economic models and innovative tools to successfully support launch reimbursement and access requirements, Manage multiple projects and budgets to target and interact with vendors to execute projects, Determine appropriate action, execution, tracking and monitoring of projects, Attend professional meetings, as well as internal business meetings, with travel, attendance, and associated cost reimbursed dependent on active research dissemination and business objectives and need, Serve as the primary liaison between PTC, CROs, and Health Authorities worldwide (e.g., the US FDA), Provide strategic input and tactical support to expedite development, submissions, and regulatory approvals, Participate in the development of global regulatory strategies supporting development, approval, and maintenance of drugs and biologics, Participate in Health Authority (HA) interactions and assess impact ofHAfeedback, Submit and maintain regulatory applications including INDs, CTAs, NDA/BLAs, Work with matrix team members (R&D and Non-R&D) to identify solutions that meet regulatory requirements as well as commercial objectives, Provide support to the life-cycle management activities, Coordinate and facilitate site engagement calls between key investigators and Relmadas executive leadership team, Analyze and interpret evidence-based medicine, medical literature, and scientific data, Coordinate clinical information between sponsor companies and experts in the field, Build and maintain clinical knowledge of applicable therapeutic areas, and provide medical information support. 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