招贤纳士

人才理念

多元包容 团队精神 帮助成长


团队建设

工作机会

关键词
职位类别
  • 岗位名称
  • 需求专业
  • 工作地点
  • 人数
  • 发布时间
  • Sr. Scientist/Principal Scientist in Computational Chemistry
  • Computational chemistry, or chemistry, biochemistry, biophysics with a computational focus.
  • 深圳/佛山
  • 若干
  • 2021-08-31
  • >

Required Experiences and Skills

• Creatively apply computational approaches to problem-solving to advance drug discovery programs.

• Experience of general molecular modeling techniques with software packages (e.g. MOE, OpenEye or Schrodinger), including docking, homology modeling, ligand-based and structure-based design, quantum mechanics, QSAR / machine learning, and molecular simulation.

• Scientific programming (e.g. Python, Pipeline Pilot) is preferred.

• Excellent oral and written communication skills.

• Track record of publications and presentations.



Education

PhD. in computational chemistry, or chemistry, biochemistry, biophysics with a computational focus. 


申请该职位
  • Toxicology Head
  • Toxicology
  • 深圳/佛山
  • 若干
  • 2021-08-31
  • >

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

申请该职位
  • Clinical Trial Assistant (CTA)
  • 临床医学、药学
  • 深圳/佛山
  • 若干
  • 2021-08-31
  • >

工作职责:

1、 负责临床试验机构立项和伦理上会的资料准备工作;

2、 管理公司临床试验TMF文档,如:临床试验研究资料的收集、扫描、复印、归档和维护等;

3、 负责临床试验项目的支持类工作,如试验所需设备的管理、物资的管理和调配、试验用药的管理等;

4、 临床试验相关会议和培训的协调与组织,如:研究会议的安排和整理会议纪要等;

5、 协助临床部负责人制定部门规范性文件,包括SOP的编辑,空白表格绘制等;

6、 协助项目经理进行项目进度管理(如整理项目进度,撰写会议纪要,更新项目管理表格等);

7、 根据部门需要,完成其他上级交办的工作。


任职要求:

1、 拥有GCP资格证书优先,临床医学、药学相关专业本科以及以上学历;

2、 熟悉临床试验流程及国内相关法律法规;

3、 良好的中英文表达能力,能整理基本英文文件;

4、 熟练掌握Word、office等办公软件及临床试验常规涉及的设备;

5、 良好的表达能力、沟通和协调能力,有良好的服务意识以及较强的应变能力,具有较强的独立工作能力和团队合作精神;

6、 具有较好的信息收集能力,关注细节,具有良好的执行力。

申请该职位
  • 总裁办助理
  • 生物医药、管理学
  • 佛山
  • 1人
  • 2021-08-31
  • >

岗位职责:

1、 独立有效的协助总裁处理综合、协调各部门工作和处理日常事务;

2、 负责总裁个人行程安排的管理;

3、 负责处理、安排并及时提醒总裁参加公司内外各类商务、行政活动;

4、 负责拜访总裁的客户接待安排,客户酒店、用餐、出行等的统筹安排;

5、 协助总裁协调公司内外部工作协调与资源调配,确保项目高效率推动。

岗位要求:

1、本科及以上学历,985高校毕业,生物医药,管理等相关专业;

2、2年以上总裁助理工作经验

3、职业方向比较明确,为人诚信、务实,注重细节,责任心强,执行力强;

4、英语听说读写熟练,熟练使用办公软件

5、时间观念强,抗压能力强;

6、具备优秀的思维逻辑及沟通协调能力、良好的原则性和灵活性;

7、形象气质良好,熟悉商务礼仪,言谈举止得体。

申请该职位
  • 项目经理
  • 药学相关专业
  • 佛山
  • 1人
  • 2021-08-31
  • >

岗位职责:

1贯彻落实所负责项目的管理工作和职责范围内的项目管理工作,组织项目参与各单位制定项目规划、项目预算,制定项目整体Timeline,撰写项目立项报告

2、负责临床前各项目的日常管理工作,按照项目制定的计划跟进和督促实施,保证项目进度符合项目计划

3、负责项目会议的组织,协调解决项目进度中相关问题,并及时反馈项目进度情况给项目负责人和公司领导

4、负责项目实施和进展过程中与公司内部各部门和外部合作单位的沟通、协调、跟踪和反馈,确保项目按计划进行

5、根据项目预算,协助进行项目支出的统计,核算项目费用,控制项目成本

6、负责项目资料的整理归档。



岗位要求:

1、药学相关专业,硕士及以上学历,3年及以上相关岗位工作经验

2、具备新药临床前研发项目管理经验

3、具有较强的沟通能力、执行能力和团队合作精神,工作积极主动,责任心强


申请该职位
  • HRD
  • Human Resources
  • 佛山
  • 2021-08-31
  • >

Responsibilities:

1、Developing and implementing strategic human resources policies in line with organizational objectives.

2、Organization review and workforce planning based on short term & long term business strategy.

3、Developing employee benefits programs and incentive plans to attract and retain talents.

4、Designing and directing employee training and development programs to help grow and develop employees.

5、Managing smooth human resources operations by recruiting, selecting, orienting and training staff.

6、Manage personnel cost to improve the organization efficiency.

7、Optimize HR daily operation process to better support business.

8、HR team management to improve team capabilities.

9、Employee relations management.


Qualifications:

1、Bachelor Degree or above in Human Resources or related major.

2、8+ years of experience in the HR field in biotech/pharmaceutical companies.

3、Extensive experience in the overall management of Human Resources.

4、Strong leadership, excellent communication skill, passion for challenges.

5、Proficient in both written and spoken English.

申请该职位