Cultural Life
Work Environment
At KANGABIO, we provide a warm and harmonious working environment with a great team atmosphere.
Annual Meeting
Our annual gala bridges past and future, with employees and their families celebrating together.
Academic Exchange
At KANGABIO, we offer diverse technical and professional training to help employees grow rapidly.
Teambuilding
Through team building activities, team cohesion can be cultivated, mood can be relaxed and body can be adjusted, and the comprehensive ability of personal life can be improved.
Open Positions
Join us in advancing biomedical innovation
Senior ADC Research Scientist
Job Description
1. Responsible for the development and optimization of small-molecule drug development and macromolecule conjugation processes.
2. Participate in developing necessary purification processes to remove impurities generated during ADC manufacturing, and take part in establishing analytical methods for ADCs.
3. Design and optimize experimental protocols, analyze technical issues, report experimental progress in a timely manner, and complete laboratory records and reports as scheduled.
4. Lead or assist in the construction and optimization of relevant technical platforms, and be in charge of the operation and maintenance of related instruments.
5. Manage project timelines and coordinate with cross-functional departments to drive project delivery.
6. Proactively complete other assigned tasks.
Requirements
1. PhD degree in Chemistry, Chemical Engineering, Biochemistry or related majors; outstanding masters may be considered, with at least 3 years of relevant working experience.
2. Hands-on experience in antibody-drug conjugation process development and familiarity with biopharmaceutical manufacturing workflows.
3. Capable of summarizing, organizing and processing complex datasets.
4. Strong technical innovation mindset and independent working ability, detail-oriented and highly responsible.
5. Good English reading and writing skills, proficient in reviewing professional English literatures.
6. Excellent communication skills and strong teamwork spirit.
Clinical Medical Manager
Job Description
1. Participate in drafting clinical trial protocols, investigator brochures, informed consent forms, case report forms and other study documents.
2. Be responsible for collecting, sorting and analyzing medical information to support the formulation of marketing strategies.
3. Revise medical documents based on feedback from principal investigators (PIs), ethics committees, medical directors, clinical monitoring departments and other relevant parties.
4. Track efficacy and safety data, and review clinical study reports.
5. Review protocol deviations and operational consistency to ensure medical compliance with the study protocol.
6. Regularly update the medical knowledge base to maintain timeliness and accuracy of information.
Requirements
1. Master’s degree or above in Medicine, Pharmacy, Oncology, Molecular Biology or other related disciplines;
2. At least 1 year of working experience in the medical field; candidates with full-cycle participation in Phase I oncology clinical trials are preferred;
3. Candidates with medical work experience in innovative drugs related to immunotherapy are preferred;
4. Excellent communication skills and strong teamwork spirit;
5. Proficient in office software, with solid capabilities in document editing and report writing;
6. Quick learner able to master new knowledge and skills efficiently;
7. Fluent in English listening, speaking, reading and writing, capable of reading English academic literatures;
8. Sound professional ethics and professionalism, able to work under moderate pressure.
Clinical Research Associate (CRA)
Job Description
1. Responsible for full-cycle monitoring of clinical trials in oncology, ensuring compliance with ICH-GCP and relevant regulations issued by the National Medical Products Administration (NMPA).
2. Independently manage the full-process work of study sites, including but not limited to site selection, site initiation, routine monitoring and close-out visits.
3. Conduct monthly on-site monitoring visits to guarantee the quality, progress and compliance of clinical trial data in line with the study protocol.
4. Establish a sound adverse event monitoring system to ensure 100% timely reporting of serious adverse events (SAEs) within required timeframes.
Requirements
1. Bachelor’s degree or above in Clinical Medicine, Pharmacy or related disciplines, with 1–3 years of working experience as a Clinical Research Associate (CRA) on solid tumor projects.
2. Proficient in Response Evaluation Criteria in Solid Tumors (RECIST 1.1), with full participation in at least 2 Phase I–II oncology clinical trials.
3. Excellent project management skills, able to travel over 50% of the time, and adept at coordinating multi-center clinical studies.
4. Possess a valid GCP training certificate, and be familiar with the latest technical guidelines for oncology clinical trials issued by the Center for Drug Evaluation (CDE) of the National Medical Products Administration.
R&D Project Manager
Job Description
1. Responsible for the overall planning and execution of oncology R&D projects to ensure on-time delivery.
2. Lead the team in new drug research and development, including but not limited to experimental design, data analysis and result interpretation.
3. Maintain effective communication with internal and external collaborative institutions to drive project progress.
4. Manage project budgets and cost control to maximize project economic benefits.
5. Compile project reports and relevant documents, and report project progress to senior management.
Requirements
1. PhD or above in Biomedicine or related disciplines; candidates with oncology drug R&D experience are preferred.
2. Over five years of pharmaceutical R&D experience, including a minimum of two years in a leadership role.
3. Familiar with the full drug development workflow and possess in-depth expertise in the oncology field.
4. Strong team management and leadership skills, capable of motivating team members and driving project delivery.
5. Excellent communication, coordination and project management capabilities.
6. Fluent in English listening, speaking, reading and writing for international academic exchanges.
7. Highly responsible and resilient under pressure, able to work efficiently in a fast-paced working environment.