Responsibilities:

1. Improve organizational structure, establish and manage a talent team, and provide training and technical guidance;  

2. Investigate the clinical feasibility and risk assessment of LNC’s projects, and provide medical advice for preclinical research, considering clinical needs and translational medicine;

3. Draft and revise relevant materials/documents for clinical research projects (including but not limited to Protocol, IB, ICF, CSR, and other registration materials);

4. Communicate with clinical experts, clinical pharmacology experts and evaluation experts, and provide scientific and regulatory support for clinical study and design; 

5. Provide protocol-related medical training and support to team members and/or investigators.

Qualifications:

1. Applicant should majored in Clinical Medicine with Master’s or Doctoral Degree; at least 3 years of hospital working experience is preferred;

2. At least 3 years of working experience as a Medical Director for an anti-tumor innovative drug  R&D Sponsor or CRO companies;

3. Fluent in English: oral, read, written.

Responsibilities:

1. Managing the entire process of medical affairs for clinical trial projects;

2. Draft, review, and revise Protocol, IB, ICF, CSR, and other related materials for clinical studies; 

3. Investigating competing clinical trial products, analyzing medical registration strategy, and planning.  

Qualifications:

1. Applicants should have a Master's degree or above in Clinical Medicine/Pharmacy; a background om clinical medicine is preferred; experience in drafting Protocol, IB, and other clinical materials is preferred;

2. Fluent in English reading and writing, and able to read English literature proficiently; 

3. Good communication skills and ability to work in a team. 

Responsibilities:

1. Full process management of medical affairs for clinical trial projects;

2. Writing, reviewing and revising protocols, IB, ICF, CSR, and other related materials in each phase;

3. Investigating clinical trials of competing products, analyzing clinical application strategies and planning.  

Qualifications:

1. Applicants with a Masters degree or above in Clinical Mdeicine/Pharmacy, a background in clinical medicine, or experience in writing clinical trial protocol, IB and other data is preferred;

2. Fluent in English reading and writing, and proficient in reading English literature;

3. Good communication skills and teamwork spirit.

Responsibilities:

1. Familiar with the clinical trial process, able to communicate with CROs in a timely manner, and actively promote the clinical trial process;

2. Monitor the entire clinical trial process from Study Start-up (SSU) to Study Closeout;

3. Participate in the review and revision of clinicals trial protocol for all clinical trial phases;

4. Assist in pharmacovigilance-related work. 

Qualifications:

1. Applicants with Bachelor's Degree or above in Clinical Medicine or Pharmacy related major; at least 2 years of experience in CRA/CRC; nuclear medicine experience and PM experience is preferred;

2. Good communication skills and ability to work in a team.

Responsibilities:

1. Experimental study of small animal molecular imaging: responsible for part of the experimental plan drafting, analyzing the experimental data, and completing the experimental reports, etc;

2. Management of experimental data, related documents and records of molecular imaging laboratory: draft relevant SOP and records of molecular imaging experiments, familiar with the SOP of this position, fill in daily original records and various experimental instrument usage records, and provide training for related experimental personnel; 

3. Daily safety affairs and equipment management of the molecular imaging room.

Qualifications:

1. Master’s Degree or above, with PET/CT, SPECT/CT, MRI, and other molecular imaging instruments experience, proficient in instruments operation, and with good problems-solving skills. 

2. Majored in Molecular Imaging, Pharmacology, Veterinary Medicine, Animal Medicine, etc.

Responsibilities:

1. Responsible for the R&D and exploration of antibody and small molecule chelator conjugation technology, and continuous optimization of conjugation technology, including but not limited to research and exploration of site-specific antibody conjugation platform and other chemical conjugation technologies; 

2. Participate in the preliminary purification process of antibody radionuclide conjugates and the development of analytical methods;

3. Responsible for drafting and revising coupling and purification related operation guidelines, and instrument operation guidelines, etc.; 

4. Report the experimental results and complete the experimental records and reports.

Qualifications:

1. Master's or Doctoral degree in Organic Chemistry, Pharmaceutical Chemistry or other related majors, with basic understanding of biochemistry, molecular biology, etc.; 

2. Work experience in the field of conjugation technology, especially in site-specific conjugation. Applicants with a Master’s Degree require at least 2-5 years of work experience; a Doctoral Degree requires at least 1 year of work experience. Priority will be given to applicant with experience in antibody radionuclide conjugation related work; 

3. Applicants with a certain understanding and experience in the purification or analysis of antibody-drug conjugation is preferred; 

4. Good communication and execution skills; 

5. Have a diligent and studious attitude, and able to actively discover, analyze and solve problems in work.

Responsibilities:

1. Carry out research and development of radiopharmaceuticals, radiolabeling methods exploration, formulation optimization, process and product performance improvement, etc.; 

2. Independently design experiments, analyze data, generate reports, and solve problems during experiments.

Qualifications:

1. Master’s degree or above, with relevant background knowledge in Pharmacy, Analytical Chemistry, Radiochemistry, Imaging, Nuclear Technology Applications, and other related fields.

Responsibilities:

1. Responsible for the suspension culture of CHO cells and 293 cells, and for developing the SOP for cell culture room;

2. Carry out cell thawing, cell culture expansion, cryopreservation, transfection, and other related work based on the company’s project plan; 

3. Responsible for the screening of transiently transfected and stably transfected cell lines for antibody projects;

Qualifications:

1. Master‘s degree or above, professional background in Biology and other related fields, WITH antibody-related experience, earnest and willing to establish a team at an early stage; 

2. Experience in antibody purification is preferred, outstanding new master‘s graduates are welcome (Master’s research with experience in antibody expression).

Responsibilities:

1. Design, establish and implement research protocols related to in vitro activity and efficacy evaluation of antibody macromolecule drugs; 

2. Explore and verify the biological function and mechanism of related targets.

3. Write relevant experimental records and research reports.

Qualifications:

1. Master‘s degree or above in Cell Biology, Immunology, Pharmacy or other related biology majors;

2. Familiar with in vitro pharmacodynamic evaluation of drugs, have solid experimental skills, and cytological experience in cell culture, proliferation inhibition, tumor killing, and other areas; proficient in ELISA, flow cytometry, and other detection technologies; and use commonly used biological analysis instruments such as flow cytometry and enzyme-linked immunosorbent assay (ELISA) independently; 

3. Applicants with experience in BLI/SPR protein binding activity analysis platform are preferred; 

4. Ability to conduct project research, independently design and implement R&D programs. 

Responsibilities:

1. Participate in the design of project experimental plans and complete the experimental process according to project requirements;

2. Provide complete and reproducible experimental records and reports; 

3. Participate in the writing of registration materials and other related work;

4. Participate in process scale-up and process handover of production enterprise;

5. Participate in the improvement and optimization of the company’s existing product processes. 

Qualifications:

1. Pharmaceutical or Chemical related majors, Bachelor’s degree or above, at least 3 years of synthesis work experience;

2. Familiar with organic synthetic chemistry, synthetic experimental operations, and spectral analysis, and able to work independently;

3. Ability to plan experimental projects and design experimental plans;

4. Applicants with experience in peptide synthesis, process development of innovative drugs, and CTD materials writing are preferred; 

5. Proficient in using office software and searching Chinese and English literature.

Responsibilities:

1. Establish quality standards for new drugs and generic drugs;

2. Routine testing, analysis method development, and methodology validation of APIs and preparations; 

3. Quality comparison research and stability analysis;

4. Instrument procurement research and instrument document preparation;

5. Daily management of laboratory affairs;

6. Preparation of registration materials for the quality research section and other related work.

Qualifications:

1. Analytical Chemistry or related majors, Bachelor’s degree or above; 

2. Have experience in drug analysis or engage in related research; 

3. Proficient in using drug analysis-related instrument, and understand the relevant processes of drug analysis.