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工作職責(zé)：

負(fù)責(zé)歐美的BD業(yè)務(wù)，

1. 歐美BD項目源開拓、項目對接，篩選評估談判；

2. 協(xié)助歐美BD開展，項目對接，初步評估，交易談判；

3. 協(xié)助整理項目資料，信息搜集，熟悉行業(yè)，有項目源，能協(xié)助談判。

任職要求：

1. 碩士以上學(xué)歷，生物、化學(xué)、藥學(xué)、醫(yī)學(xué)等生物醫(yī)藥相關(guān)專業(yè)；

2. 5年以上BD經(jīng)驗，擁有頂級公司的生命科學(xué)/醫(yī)療領(lǐng)域的戰(zhàn)略咨詢、跨國業(yè)務(wù)拓展或投資銀行經(jīng)驗優(yōu)先；

3. 了解盡職調(diào)查、資產(chǎn)評估、聯(lián)盟整合和投資組合管理的過程，結(jié)合科學(xué)和商業(yè)頭腦；

4. 具有良好的組織和人際交往能力，溝通能力強(qiáng)，有良好的談判和交易談判能力，在壓力下能保持冷靜；

5. 流利的英語聽說讀寫能力。

Responsibilities:

1. Drive small molecule medicinal chemistry program on:

Molecular design and SAR evaluation Implementation of organic syntheses and problem solving

Directing a team of internal and external (CRO) chemists to execute chemistry plan Preparation of experimental for report and patent filing

Interacting cross-functionally to collect vital data Presenting resulting and data in program meeting and to review committee

2. Serve as chemistry leader on:

Participating on cross-functional project teams to evaluate, prioritize and set strategy to positively influence project direction and timelines

Build strong working relationship with internal and external colleagues and organizations Training, building and growing the chemistry team, and ensuring maximal productivity

3. Acting as a resource and mentor to team members

Managing external (CRO) FTE Sourcing of reagent and its procurement cost effectively

Drive quality and speed to meet departmental and company goals

Grow to become an influential drug hunter and scientist

Qualifications:

1. PhD in Organic or Medicinal Chemistry

2. At least 3 years industry experience in small molecule medicinal chemistry

3. Excellent communication skill

4. Sufficient language proficiency to present in English

Responsibilities:

1. Ensure that the Quality Management System (QMS) is effectively implemented and complies with all applicable domestic and international laws, regulations and standards

2. Contribute to managing and improving QMS

3. Support QMS-related actions including but not limited to

  Preparing, reviewing and implementing quality assurance policies and procedures

  Assisting in vendor quality management including planning/performing routine inspections and audits

  Conducting Incident Investigation, Root Cause Analysis, and Impact assessment

  Documenting quality assurance activities and creating/approving audit reports

  Providing/Coordinating specific quality trainings to relevant employees

Qualification requirements:

1. Minimum 3 years of experience in QC and QA activities in the pharmaceutical, biochemical, or food industry

2. Bachelor degree or higher in science related field with laboratory experiences

3. The capacity for new experiences and challenges

4. Willingness to take increasing responsibilities while learning at the job

The ability to commit to the team's mission over individual interests

Responsibilities:

1. Develop, validate, optimize and execute cell-based assays to support SAR in lead identification and optimization.

2. Design and carry out explorative, mechanistic research on oncogenic target validations, biomarker discovery, drug resistance and beyond

3. Analyze experimental data to evaluate new molecules’ potency in target engagement in cellular assays.

4. Maintain accurate records of experiments, analyze and interpret the results, present summaries, and generate reports of the studies.

5. Work in close collaboration with discovery team and communicate results in a timely manner.

6. Supervise research associates in designing, executing experimental plans.

Qualifications:

1. PhD in molecular biology, cell biology, cancer biology, immuno-oncology or other biological disciplines.

2. PhD (Preferred) with 5-10 experience in drug development or immunoncology research experience.

3. Experience with molecular/cell biology techniques such as immunoblots, in-cell western, ELISA and bio-luminescence as well as other detection methods.

4. Experience in cellular assay development, optimization, validations.

5. A major plus for expertise in flow cytometry and high content imaging techniques.

6. Ability to manage multiple projects and proficiency as a scientific leader that designs, execute or lead associate to execute, and manages research plans,

7. Highly independent and organized with proficient verbal and written communication skills

崗位職責(zé)：

1. 獨立有效的協(xié)助總裁處理綜合、協(xié)調(diào)各部門工作和處理日常事務(wù)；

2. 負(fù)責(zé)總裁個人行程安排的管理；

3. 負(fù)責(zé)處理、安排并及時提醒總裁參加公司內(nèi)外各類商務(wù)、行政活動；

4. 負(fù)責(zé)拜訪總裁的客戶接待安排，客戶酒店、用餐、出行等的統(tǒng)籌安排；

5. 協(xié)助總裁協(xié)調(diào)公司內(nèi)外部工作協(xié)調(diào)與資源調(diào)配，確保項目高效率推動。

崗位要求：

1. 本科及以上學(xué)歷，985高校畢業(yè)，生物醫(yī)藥，管理等相關(guān)專業(yè)；

2. 2年以上總裁助理工作經(jīng)驗

3. 職業(yè)方向比較明確，為人誠信、務(wù)實，注重細(xì)節(jié)，責(zé)任心強(qiáng)，執(zhí)行力強(qiáng)；

4. 英語聽說讀寫熟練，熟練使用辦公軟件

5. 時間觀念強(qiáng)，抗壓能力強(qiáng)；

6. 具備優(yōu)秀的思維邏輯及溝通協(xié)調(diào)能力、良好的原則性和靈活性；

7. 形象氣質(zhì)良好，熟悉商務(wù)禮儀，言談舉止得體。

Primary Responsibilities

? Provide preclinical safety expertise and strategy for pre-clinical and clinical development programs from pre-clinical drug candidate selection to IND enabling and clinical trials

? Apply a broad understanding of toxicology, pharmacology, DMPK and regulatory sciences to design all types of toxicology studies required to support drug development of biopharmaceuticals

? Ensure that the preclinical safety plan is aligned with the clinical development plan and regulatory guidelines (ICH, FDA, GLP, etc.)

? Serve as Preclinical Safety team leader for multiple programs and contribute to the program’s goals and deliverables

? Identify and manage contract research laboratories (CRO) for preclinical safety studies; review reports; ensure they are using systems and processes in compliance with all relevant regulatory standards

? Write and review documents for INDs / regulatory section submissions; represent the company as the pre-clinical toxicology expert before regulatory authorities

? Serve as a subject matter expert to provide input for due diligence of potential external partnership programs

Qualifications

? 10+ years of combined toxicology, drug development and regulatory experience in a biotech, biopharmaceutical or CRO setting

? Extensive knowledge and expertise with in vitro and in vivo toxicology study conduct and reporting

? Familiar with applicable regulatory guidelines; prior experience with regulatory agency interactions is preferred

? Proven leadership and management skills, including the ability to interact effectively with CRO personnel and internal/external experts for the conduct of toxicology studies

? Good communication and technical writing skills in English. Capable of engaging in scientific dialog among large groups of scientists, senior management, and external scientific experts

Education

? Ph.D. or equivalent in Toxicology or closely related field

? Toxicology board certification is a plus