mjcbac@hchc.edu, 2023 Mary Jaharis Center for Byzantine Art & Culture at Hellenic College Holy Cross. If, however, you have submitted your PhD and began your PhD course before 31 August 2017 you must submit as your fellowship dissertation your PhD thesis either that submitted for examination or that officially accepted, after correction as the approved doctoral thesis. It is the goal of the program to provide the fellow with the skills and tools necessary for a successfulcareer in the pharmaceutical industry. Fellows under Title A who reside within the University precincts and devote themselves to study and research receive a stipend. She is excited for the opportunities to collaborate on a multidisciplinary team and expand her unique skillset. Emeritus Fellowships are awarded to Fellows of the College who have held office for at least fifteen years before retiring post, or for at least twenty years before resigning. The University of Cambridge is a public collegiate research university in Cambridge, England.Founded in 1209, it is the world's third-oldest university and is ranked widely as one of the best universities in the world; as of 2023, it is ranked second-best in the world by QS World University Rankings. 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. I am an Assistant Professor at the Department of Psychology, Maynooth University, with research expertise in the area of child and youth mental health, and a particular interest in self-harm and suicide. She hopes to continue leveraging her experiences and looks forward to being a part of a diverse and passionate team. By clicking Accept All, you consent to the use of ALL the cookies. Gain proficiency in conducting comprehensive literature searches. Upon successful completion of the fellowship program, a certificate of completion will be awarded by St. Johns University College of Pharmacy and Health Sciences and Pfizer. She earned her Bachelor of Science degree in Molecular Toxicology from the University of California, Berkeley, and her Doctor of Pharmacy degree from the University of Michigan College of Pharmacy. Brittany Nghiem, Pharm.D.,is the 202123 St. Johns University/American Regent, Inc. Industry Fellow in Medical Affairs. Referees should provide the details for four readers, at least two of whom should not work at the University of Cambridge. 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. Research Fellows normally obtain their doctorates during the early stage of their Research Fellowship, and move on to pursue postdoctoral research. Pharmacists in the Department of Medical Affairs provide efficient and unbiased medical information concerning the companys pharmaceutical products to healthcare professionals, consumers, and internal associates. Registered Charity No. She also served as Media Chair forScript Your Future, an endeavor that went on to earn the 2020 Script Your Future National Award. 6 Those longlisted will be invited to submit a piece of work (c. 10,000 words) including copies of text, chapters, articles or DOIs. Dr. Gharibian was raised in Los Angeles, CA, and is excited to make the move to New York City. Candidates who have had an article published often decide to submit it, whereas some other, unpublished piece of work might have given a better impression of the range and ambition of their work and would have been more likely to secure them a place on the shortlist. There is no formal word limit for fellowship dissertations, but in most cases candidates are unlikely to help their case by submitting a very long piece (over about 100,000 words). She hopes to leverage her variety of experiences to contribute to the HEOR/market access space. Information about how to apply and further details about the process, including the timetable for submitting applications, can be found in these further sections. Develop an understanding of the regional landscape, including specialties involved in care of patients, Assist in answering medical information requests. Junior Research Fellows. My research explores how peers, parents, schools, and healthcare providers can best support young people's mental health. The Fellowship is open to those whose research is principally in one or more of the following subject areas: Anglo-Saxon, Norse & Celtic; Architecture; English (limited to pre-1800 literature); Linguistics; Modern & Medieval Languages; Music; Philosophy. A cookie set by YouTube to measure bandwidth that determines whether the user gets the new or old player interface. to arrive by the deadline date. You also have the option to opt-out of these cookies. The applications committee will automatically put forward for consideration any applicant for any of the subjects listed above that may be eligible. The College currentlypartnerswith sixpharmaceutical industry leaders:American Regent, Inc.; Pfizer Inc.; Relmada Therapeutics, Inc.; Allergan Aesthetics, an AbbVie Company; PTC Therapeutics; Myovant Sciences. She will work on bringing to market a novel therapeutic option for patients living with Major Depressive Disorder. The College wishes to encourage applications from a wide range of candidates and the Fellowships are available in all branches of University studies. If non-resident, the use of a study, free of charge, in College may be available. All students and the more than 100 full-time faculty members live on the grounds. Applicants who do not have an automatic right to work in the United Kingdom should note that, although they would still be elected to a Fellowship on 3 October 2023, employment and the payment of stipend cannot commence until appropriate leave to enter or remain has been granted under the Home Offices immigration rules. She also served as Media Chair for Script Your Future, an endeavor that went on to earn the 2020 Script Your Future National Award. Quantserve sets the mc cookie to anonymously track user behaviour on the website. 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. The Fellowships are intended for researchers early in . 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). We provide students with a world class education in a diverse, friendly and lively environment where they can exceed their own expectations. Annual Report home; Who we are; Facebook. 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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