奖学金

的 Innovate in 药物警戒 Fellowship is a post‐graduate training program designed to train pharmacists in pharmacovigilance, with research 和 field‐based medication safety learning opportunities. 的 program provides two (2) year fellowships. 

A new approach to pharmacovigilance training, it launched in 2021 as a collaboration between pharmacists, safety scientists 和 data scientists from academia, industry 和 the US Food 和 Drug Administration (FDA). 的 fellowship distributes training activities over a two‐year period including 12 months at a life sciences company; four months at ACPHS; 和 eight months at the FDA.

Designed to build on a pharmacist’s core knowledge, fellowship emphasizes three main areas of intensive training 和 competency development:

• 药物警戒
• 药物安全
• 数据科学

Typical activities include safety surveillance 和 adverse event reporting, monitoring safety 和 quality of patient care 和 medication use systems, 并对 FDA’s adverse event reporting system (FAERS) data.

欲了解更多，请访问 BeiGene.

的 Crinetics Quality Assurance (QA) Fellowship provides two (2) years of comprehensive practical h和s-on biopharmaceutical training 和 fosters an environment of learning within a fast-growing biopharmaceutical company.

的 fellow pairs with QA leaders to support initiatives, provide QA oversight for various clinical trials 和 study teams, 和 work cross-functionally with all departments. 的 collaborative environment offers the fellow an enduring network 和 exposure to all aspects of the drug development process.

学习目标:

• Support 和 participate in GxP activities
• Develop tools for tracking key performance indicators, 创建KPI指标图表, 和 collect KPI data from records 和 the QA team.
• Track status 和 progress of the Annual Audit Schedule ensuring that audit deliverables are completed in a timely manner.
• Ensure accurate filing of GxP audit records, 调查报告, associated corrective 和 preventive actions (CAPAs), 和偏差.  
• Assist in GxP Inspection Readiness Activities including the tracking 和 scheduling of Story Board development 和 reviews.
• Work with QA team to identify enhancements to Vendor tracker, 认可供应商名单, 以及其他跟踪工具.
• Assist Document Control with formatting, preparation 和 review of controlled procedures within the EDMS.
• Work collaboratively with QA team to identify business processes 和 areas that require improvement 和 implement appropriate methods 和 tools to increase efficiencies.
• Support EDMS System Administrator with user testing of system configuration changes.

申请材料:

• 意向书
• Two (2) letters of recommendation (LOR) submitted via email directly from each reference.
• 简历(CV)
• Unofficial pharmacy school transcripts
• Any additional materials that the c和idate feels would be useful to the interview committee may be submitted.

最后期限:

• 的 dates for submitting applications will be listed prior to the new search starting.
• Interviews will be conducted on a rolling basis upon application review. Early application submission is highly encouraged. All rounds of interviews will be conducted virtually.

的 Clinical Pharmacology Fellowship is recruiting for one position. A strong preference for hybrid position in San Diego, CA总部, is desired but open to remote requests. 的 fellowship start date is July 1, 2023.

职位描述: 

的 Clinical Pharmacology Fellowship provides two (2) years of comprehensive practical h和s-on biopharmaceutical training 和 fosters an environment of learning within a fast-growing biopharmaceutical company. 的 fellow will be paired with leaders in the Clinical Pharmacology functional area 和 will have the opportunity to gain direct experiences in plans, 设计, implements 和 analyzes routine clinical pharmacology studies to advance scientific 和 practical knowledge, to collaborate cross-functionally supporting various nonclinical 和 clinical studies, 和 gain broad insight on how clinical pharmacology impacts various aspect of drug discovery 和 development. 的 collaborative environment will offer the fellow an enduring network 和 exposure to all aspects of the drug development process.

学习目标:

• Educational experience in clinical pharmacology study design/protocol development, 数据收集, 数据分析.
• H和s-on experiences in non-compartmental analysis (NCA) of routine nonclinical 和 clinical studies to advance scientific knowledge, in collaboration with other team members.
• With guidance 和 supervision from senior clinical pharmacology staff, draft 和 review study related documents or applicable sections pertinent to clinical pharmacology, e.g., synopsis, protocol, PK/TK reports, SAP, TFLs, 和 CSR, etc.
• With guidance 和 supervision from senior clinical pharmacology staff, supports preparation of material 和 performs additional analyses as required to support regulatory interactions.
• Participate in literature search 和 regulatory guidance 和 review to support clinical pharmacology study design 数据分析.
• Participate in research 和 development projects with various modeling 和 simulation techniques 和 programming software.
• Successfully complete selected workshops 和 courses in pharmacometrics 和 related areas, to ensure base knowledge of the field.
• Author a minimum of one peer-reviewed poster with preparation
• Made at least one formal presentation to peers at a seminar, workshop or national meeting related to research completed to date.

申请材料: 

C和idates must submit all the following application materials to Albany College of Pharmacy 和 健康科学 to 达伦.grabe@ycdwkj666.com 和 伯纳德.tyrrell@ycdwkj666.com.

• 意向书 
• Two (2) letters of recommendation (LOR) submitted via email directly from each reference.
• 简历(CV)
• Unofficial pharmacy school transcripts
• Any additional materials that the c和idate feels would be useful to the interview committee may be submitted

最后期限:

• We are accepting applications between March 20th to April 7th, 2023. Please send all application materials to 达伦.Grabe@ycdwkj666.com 和 伯纳德.tyrrell@ycdwkj666.com.
• Interviews will be conducted on a rolling basis upon application review. Early application submission is highly encouraged. All rounds of interviews will be conducted virtually.

This two-year fellowship in biomanufacturing is a collaboration of with 教廷全球, FDA Office of Pharmaceutical Manufacturing Assessment (OPMA) 和 Albany College of Pharmacy 和 健康科学. 

的 partnership of a global pharmaceutical company with a regulatory agency 和 an academic institution provides a rich 和 rewarding experience for the fellow. 除了, three partners build on their individual strengths 和 common objectives to create compelling projects over the two-year span.

的 fellowship is ideal for a PharmD 和/or PhD holder who is interested in working in a dynamic environment with diverse cross-functional teams.

欲了解更多，请访问 教廷全球.

的 FDA Office of Pharmaceutical Manufacturing Assessment (OPMA) assures that quality pharmaceuticals are consistently manufactured over the product lifecycle. For more information, please visit the FDA Office of Pharmaceutical Manufacturing Assessment (OPMA).

最后期限:

• 的 dates for submitting applications will be listed prior to the new search starting