1. Responsible for research activities related to biology; formulate appropriate experimental plans through literature review and communication with superiors.

2. As project representative or leader, coordinate and execute projects within time and quality requirements; able to communicate effectively both internally and externally.

3. Independently analyze, interpret, summarize and compile data; maintain appropriate experimental records and documents.

4. Cooperate with other departments to promote progress of new projects.

5. Good at finding and solving problems encountered in the laboratory, writing experimental reports in both Chinese and English, and preparing materials related to patent application.

6. Train researcher/associate researcher.

7. Complete other tasks assigned by supervisor

1. Master degree or above, major in biology (molecular, cellular, neurological, immunological, etc.), pharmacy or medical related.

2. Strong autonomy, curiosity, quick-learning ability, good communication skills, love laboratory work, strong hands-on ability, team-work spirit.

3. Possess experience in cell culture, PCR, ELISA, molecular cloning, etc., or can master these skills after short-term training.

4. Candidate with experience in drug screening is preferred.

1. Responsible for research activities related to protein antibody engineering and making appropriate experimental plans through literature review and communication with superiors.

2. Assist in building the protein and antibody expression platform in the research and development stage.

3. Analyze, interpret, summarize and compile data independently; keep appropriate experimental records and documents.

4. Cooperate with other departments to promote progress of new projects.

5. Good at finding and solving problems encountered in the laboratory, complete the writing of experimental reports in Chinese and English, and prepare relevant materials for patent application.

6. Complete other work assigned by supervisor.

1. Bachelor degree or above, major in biochemistry or protein engineering.

2. Strong autonomy, curiosity, quick-learning ability, good communication skills, love laboratory work, strong practical ability and team spirit.

3. Experienced in protein expression and purification.

4. Familiar with various methods commonly used in the process of protein purification and the characterization methods and technologies of protein samples.

5. Candidate with experience in establishing in vitro enzyme test system is preferred.

1. Lead the team to complete construction of drug evaluation system in vitro and in vivo, lead the team to complete drug preclinical screening and efficacy evaluation, and make contributions to the field of intellectual property rights through patent application.

2. Responsible for the design of in vitro and in vivo experiments related to drug biology, data interpretation, report review, and answer questions related to the project.

3. Responsible for managing the biological team, training and managing the researchers to assist them in their duties.

4. Participate in clinical projects and biology-related research and promote clinical project progress

5. Support document compilation related to innovative drug registration.

6. External project evaluation or any other BD support.

7. Complete experimental management and other tasks arranged by the company.

1. Have a PhD degree in cell/molecular biology, pharmacology, immunology or related fields; have published high-level articles in related fields.

2. Familiar with the process of drug discovery; master relevant experimental techniques and methods, such as enzyme experiments, cell experiments, animal efficacy evaluation experiments, etc.; at least 5 years (Director I) or 10 years (Director II) relevant working experience required.

3. Actively follow up the latest development of related projects and guide project progress

4. Follow up new techniques or methods and apply them to project research.

5. Experienced in team management, strong ability of organization, management and coordination, analysis and problem solving.

6. Both Chinese and English can be used as working languages.

1. Responsible for selection and approval of biological drug research and development projects, target determination, screening and evaluation; solve key technical problems in the process of project development;

2. According to the progress and requirements of Ark's new drug research and development, develop experimental plans and schemes to ensure the quality and progress of research and development;

3. Design experimental schemes, analyze experimental data, communicate with direct leaders and other relevant personnel, solve technical problems, and complete R&D tasks according to schedule requirements;

4. Responsible for preparing R&D budget, management of the operation of the R&D laboratory, procurement and maintenance of instruments, equipment, reagents and consumables.

5. Responsible for R&D team building, performance management, assessment and evaluation of department staff.

6. Responsible for training relevant R&D personnel and providing technical support to other teams in the R&D center.

7. Participate in the evaluation, investigation, and project preparation of Ark's new drug products.

1. Master’s degree or above, major in biology or pharmacy.

2. Solid theoretical foundation, clear thinking, able to design and carry out relevant research projects.

3. Experienced in R&D team management and training, able to provide guidance and training for R&D personnel.

4. Both Chinese and English can be used as working languages.

5. Good project management skills, organizational skills and team spirit, good communication skills, high sense of responsibility and professionalism.

6. Familiar with domestic and foreign development trends of biological drugs, have a deep understanding of antibody drug production quality management system, have rich experience in biological drug development, be familiar with complete biological drug development process; understand contents and procedures of clinical application.

7. Candidate with working experience in overseas pharmaceutical companies is preferred.

1. Design and plan toxicology and safety-related experiments to support assigned project development.

2. Work with CROs to develop toxicology study protocols, monitor toxicology experiments, interpret experiment data, review, and finalize reports.

3. Organize toxicology function-related documents including but not limited to studying protocols, reports and contracts.

4. Assist with setting up department SOPs and budget.

5. Evaluate and manage toxicology related CROs.

6. Assist with writing high-level toxicology and safety pharmacology summaries of Modules 2.4 and 2.6 in the IND and NDA submissions and other regulatory submissions.

7. Compliance with Good Laboratory Practice (GLP) regulations as well as internal/external guidance.

1. Master in toxicology or related field

2. At least 1 year post-graduate experience

3. Proven experience as a toxicologist in any relevant field

4. Highly organized and methodical

5. Meticulous attention to detail

6. Collaborative and exceptional problem-solving skills

7. Ability to multitask and work to tight deadlines

8. Excellent written and verbal communication skills

1. Operate in collaboration with study personnel to provide input to study protocol, perform sample size calculation, develop randomization schedule, write/review Reporting Analysis Plan, and write/review Statistical Analysis Report.

2. Participate in peer-review of work products from other statistical colleagues.

3. Oversee the process and quality of statistical work contracted out to CRO or research collaborator.

4. Collaborate with data management in planning and implementation of data quality assurance plans.

5. Perform statistical programming to validate results produced by CROs or to meet internal need of data analysis (e.g. for publication, or for optimizing assumptions for study design).

1. Master’s degree in Statistics, Math or equivalent field of study.

2. Positive working attitude.

3. Knowledge of statistical theories and application.

4. Knowledge of statistical tools such as SAS, nQuery, PASS, East.

5. Self-management skills with a focus on deliverables.

6. At least 8 years’ experience in pharmaceutical company or Clinical Research Organization (CRO) as a biostatistician or programmer.

7. Knowledge of early drug development and therapeutic areas such as respiratory and infection diseases.

1. Support data management of clinical trials, participate in the design of case report forms; construct databases and test automatic/manual verification procedures.

2. Review or write data management related documents, such as data management plan, data verification plan, external data transmission document, SAE conformance verification plan, fill in guidelines, coding rules, etc.

3. Participate in relevant project meetings, cooperate closely with the project team, and conduct relevant training as required.

4. Monitor and review the work of suppliers to ensure the quality and schedule of data management and achieve timely and high-quality delivery of all DM-related tasks.

5. Responsible for document maintenance and TMF archiving of clinical data management.

1. Bachelor degree or above, major in medicine or related field.

2. At least 4 year experience in data management in pharmaceutical industry.

3. Understand regulations/guidelines related to data management.

4. Good English oral and written communication skills.

5. Strong learning ability, independent work, communication, and coordination ability.

1. Site selection (if applicable), start, monitor clinical sites according to the clinical practice plan and GCP requirements.

2. Visit sites for monitoring and site management purposes.

3. Cooperate with development of research project recruitment plans of sites; if applicable; work with sites to adjust to project requirements, drive and track recruitment plans to enhance predictability.

4. Ensure that data sources/files and other tracking records in the study are accurate, complete and authentic, and report quality problems if necessary.

5. Manage the progress of assigned research projects, followed up registration submission and approval, recruitment, case report form (CRF) completion and submission, and data query generation and resolution.

6. Establish documents related to maintenance center management, inspection findings and action plans by submitting daily inspection reports, regular review letters and other documents related to research.

7. Other tasks assigned by leaders.

1. Bachelor degree or above in health or other related majors.

2. More than 1 year working experience, familiar with GCP and ICH regulations.

3. Good communication and coordination skills, familiar with Microsoft Office.

4. Be willing to travel frequently.

1. Formulate and implement Ark's accounting policies, accounting systems and financial systems in accordance with relevant national laws and regulations and relevant regulations of the company.

2. Supervise and review the daily accounting work of the company, including revenue recognition, cost accounting, procurement accounting, asset management, expense reimbursement and accounting, financial approval process, etc.

3. Ensure that accounting vouchers and financial statements are timely, accurate and complete, and ensure that the company's business is legal and compliant with listing compliance requirements.

4. Integrate information disclosure of financial statement data, and provide accounting data support for operation assessment and management decisions.

5. Establish internal audit mechanism and organize the annual inventory of the company.

6. Cooperate with other departments to complete the declaration, accounting, inspection and completion of government projects.

7. Promote the optimization of financial ERP system, conduct internal publicity, interpretation, promotion and implementation of various financial management systems and operation processes.

8. Other tasks assigned by leaders.

1. Bachelor degree or above in finance, accounting, economics or related major, Certified Public Accountant or equivalent.

2. More than 10 years of relevant working experience, more than 3 years of overall financial accounting work experience, more than 3 years of team management experience, pharmaceutical industry background is preferred, with English office ability, familiar with financial software, data analysis tools and office software.

3. Candidate with IPO experience in pharmaceutical industry is preferred.

4. Good professional ethics and teamwork spirit, strong communication, understanding and execution ability.

5. Sensitive to numbers