1. pre clinical safety assessment Manager / Deputy Director (working place: Shanghai or Hangzhou)

Job responsibilities
1) Be responsible for supporting the planning, design and implementation of safety assessment tests for R & D projects at different stages of the company;
2) Be fully responsible for the budget, schedule, quality and risk control of the company's pre clinical safety assessment project;
3) Expand and maintain resources with domestic safety assessment experts and safety assessment centers to ensure that problems in clinical safety assessment trials can be solved in a timely manner;
4) Be responsible for the screening and supervision of pre clinical safety assessment partners (cros), and ensure that all pre clinical safety assessment tests meet the requirements of domestic and foreign laws and regulations, especially the requirements of GLP;
5) Be responsible for the summary, review and approval of preclinical safety assessment test and the organization of relevant meetings;
6) Participate in the writing of new drug application materials such as IB and ind and the audit of regulatory agencies;
7) Represent the company in meetings with regulators and professional areas.

Job requirements
1) Master degree or above in toxicology, pharmacology, pharmacy or Immunology;
2) At least 3 years of preclinical safety assessment related working experience (Master's degree more than 5 years), and relevant experience in pharmaceutical companies or safety assessment centers is preferred;
3) Familiar with regulations, policies and procedures related to pre clinical safety assessment in GLP and ICH;
4) Experience in Sino US ind reporting is preferred;
5) Have the experience and ability to establish good working relationship with different collaborators;
6) Strong coordination and communication skills;
7) Good English reading and writing skills.

2. project leader of discovery biology

Job description:
As a core member of discovery biology department, lead at least one innovative biological macromolecular drug discovery project, from target verification / potential drug molecular identification to ind declaration.
1) Have a deep biological understanding of drug targets, determine the key scientific issues of drug discovery, and establish extensive cooperative relations with cros, universities and academic institutions to ensure the success of the project;
2) Propose, design and conduct appropriate in vitro and in vivo drug action mechanism and efficacy research for the company's tumor, infectious and autoimmune diseases (currently focusing on immune Oncology) project;
3) Establish and maintain effective cross functional relationships with other departments of the company;
4) Recruit talents and guide ≥ 2 research assistants as direct subordinates; Ensure accurate and compliant records of experiments conducted within the company and partners;
5) Report the project progress in regular project review meetings and manage the project schedule.

Job requirements
1) Doctor degree in immunology, cancer biology, cell biology and other life science related disciplines;
2) Drug R & D experience in multinational pharmaceutical companies or well-known biotechnology companies is preferred;
3) Experience in macromolecular drug identification and optimization is preferred;
4) Familiar with in vitro function test and in vivo animal model in oncology or immunooncology;
5) Experience in managing a diverse team of scientists and leading cross functional projects is preferred;
6) Have the ability to learn quickly and adapt to working in a dynamic and fast environment;
7) Excellent teamwork spirit;
8) Excellent oral, reading and written communication skills in English.

3. discovery biology research assistant

Job description:
As a key member of the early drug discovery project team, participate in at least one innovative biomacromolecule drug research project, from target verification / potential drug molecular identification to ind declaration.
1) According to the company's project research requirements, formulate experimental plans and carry out biochemical analysis and cell biology related experiments;
2) Feed back the experimental process, progress and results in time, and preliminarily analyze and process the experimental data;
3) Write experiment records in strict accordance with the company's regulations;
4) Regular work reports;
5) Accept and complete other tasks assigned by the company or superior leaders on time.

Job requirements
1) Bachelor or master degree in immunology, cancer biology, cell biology and other life science related disciplines;
2) Drug R & D experience in multinational pharmaceutical companies, cros, or well-known biotechnology companies is preferred;
3) Experience in macromolecular drug identification and optimization is preferred;
4) Familiar with in vitro function measurement in oncology or immunooncology;
5) Can conduct tests independently and master basic data analysis software (such as graphpadprism);
6) Have the ability to learn quickly and adapt to working in a dynamic and fast environment;
7) Excellent teamwork spirit;
8) Good English reading and writing skills.

4. clinical operation director / Senior Director / Vice President

Job responsibilities
1) Establish and manage clinical operation team, including but not limited to personnel recruitment, department budget formulation, training, etc;
2) As a member of the company's core management team, provide development strategy, global clinical development plan, budget and other support for projects entering clinical development;
3) From the perspective of clinical operation, participate in the writing of new drug application materials such as IB, trial protocol and ICF and the audit of regulatory agencies;
4) Establish a good working relationship with KOLs, cros and SMOs in the industry to ensure the rapid advancement of clinical projects;
5) Establish and improve the management and quality system related to clinical operation to ensure the quality and compliance of clinical operation;
6) Represent the company in meetings with regulatory bodies and professional areas.

Job requirements
1) Graduated from medical college, with experience in tumor or infectious diseases is preferred;
2) At least 8 years of relevant experience in clinical operation, working experience in pharmaceutical companies or biotechnology companies is preferred;
3) Familiar with all procedures of clinical trials, experience in phase I-III clinical trials is preferred;
4) Experience in successful and systematic management of clinical trials;
5) Excellent cross department working ability;
6) Be familiar with clinical regulations, policies and procedures in GCP and ICH;
7) Have the experience and ability to establish good working relationship with different collaborators;
8) Good English communication skills.