Careers

CBP > Careers

Let's Create
The Miracle Together

We truly believe that employees are the most valuable resource of the company and the core driving force behind the continuous development of the enterprise. Based on this belief, we provide a series of high-quality benefits for our employees.
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Comprehensive Career Development Pathways
We provide technical and managerial career development paths to offer employees comprehensive opportunities for growth and advancement.
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Highly Competitive
Salary
We implement a highly competitive salary system in the market to ensure that employees are rewarded fairly and generously for their efforts.
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Employee Medical Insurance
We prioritize the physical and mental well-being of our employees by offering high-quality health services to help them maintain a good work-life balance and quality of life.
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Cooperation & Leadership Program
We regularly organize team-building activities to foster effective communication and collaboration among employees, ultimately boosting job satisfaction and overall happiness.
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Careers at CBP

Join our multidisciplinary team of determined, passionate people.
Senior Researcher in Drug Development

Qualifications:

  1. Doctor’s degree or above in Pharmacy, Biology, or Organic Chemistry.
  2. Proficient in drug development strategies, drug design, in vitro and in vivo evaluations, with some experience in drug synthesis.
  3. Able to independently write laboratory SOPs and specification documents.
  4. Strong English reading skills, capable of extracting information from literature and providing method development services.
  5. Proficient in computer data analysis and processing.
  6. Familiar with project management thinking, experience in project management is preferred.

Responsibilities:

  1. Responsible for developing drug development strategies, including but not limited to defining customer project requirements, developing project development strategies, completing drug synthesis, screening, in vitro and in vivo evaluations, and forming a research and development team.
  2. Responsible for the training and promotion of subordinates, conducting technical capacity training.
  3. Laboratory management work, including but not limited to writing relevant SOPs, ordering reagents and consumables, managing cell rooms, and arranging experimental content.
  4. Participate in business development, assist in publicity and external negotiations of the Business Cooperation Department, provide technical support and explanations.
Apply
Senior Ligand Development Researcher

Qualifications:

  1. Doctor’s degree or above in Biology, Pharmacy, or Medicine.
  2. Over three years of experience in phage display (recent Ph.D. graduates with related dissertation topics on phage display are eligible).
  3. Proficient in phage display technology, with rich experience in phage display and screening of peptides and antibodies.
  4. Some understanding of biochemistry, in vitro experiments, etc., able to design experiments according to screening requirements.
  5. Capable of independently writing SOPs and specification documents for biological experiments.
  6. Strong English reading skills, capable of extracting information from literature and providing method development services.
  7. Proficient in computer data analysis and processing.
  8. Familiar with project management thinking, experience in project management is preferred.

Responsibilities:

  1. Responsible for platform establishment and expansion, including but not limited to building and verifying phage display and display technology, providing ligand selection for drug development projects, and forming a research and development team.
  2. Clearly define customer project requirements, develop corresponding development strategies, and closely follow project progress.
  3. Responsible for the training and promotion of subordinates, conducting technical capacity training.
  4. Laboratory management work, including but not limited to writing relevant SOPs, ordering reagents and consumables, managing cell rooms, and arranging experimental content.
  5. Participate in business development, assist in publicity and external negotiations of the Business Cooperation Department, provide technical support and explanations.
Apply
Phage Display Researcher

Qualifications:

  1. Master's degree or above in Biology, Pharmacy, or Chemistry.
  2. Over three years of experience in phage display (recent Ph.D. graduates with related dissertation topics on phage display are eligible).
  3. Proficient in phage display technology, with rich experience in phage display and screening of peptides and antibodies.
  4. Some understanding of biochemistry, in vitro experiments, etc., able to design experiments according to screening requirements.
  5. Capable of independently writing SOPs and specification documents for biological experiments.
  6. Familiar with project management thinking, experience in project management is preferred.
  7. Strong English reading skills, proficient in computer data analysis and processing.

Responsibilities:

  1. Participate in the entire cycle of drug development projects, including project establishment, planning, design, progress tracking, and completion.
  2. Fully understand project requirements, base work content on requirements, and closely follow project progress.
  3. Expand and validate the phage display and screening technology platform, solve problems in each experimental link.
  4. Summarize technical development guidance documents through the development of multiple cases.
  5. Responsible for laboratory management work, including but not limited to writing relevant SOPs, ordering reagents and consumables, and using and maintaining laboratory instruments.
Apply
Pharmaceutical Strategy Analyst

Qualifications:

  1. Doctor’s graduate with up to 3 years of work experience.
  2. Preference for majors in Pharmacy, Biology, followed by Medicine, Organic Chemistry, and other majors.
  3. Strong willingness to work and learn about new drug development.
  4. Open-minded, proactive, and willing to discuss and communicate.

 

Responsibilities:

  1. Collect and summarize information on domestic and international new drug development, establish a project strategy analysis platform based on the company's technology.
  2. Participate in and assist in company decision-making process management, provide solutions for the strategic decision-making of company projects based on the strategic analysis platform.
  3. Independently responsible for early-stage research and development projects, deepen understanding of project strategy through project implementation.
Apply
Senior Organic Synthesis Researcher

Qualifications:

  1. Bachelor's degree or above in Chemistry or related field (preference for Organic Chemistry).
  2. 4+ years of experience for Bachelor's degree holders, 2+ years for Master's degree holders, fresh Ph.D. graduates are welcome.
  3. Passion for learning and organic chemistry, familiarity with reaction mechanisms.
  4. Proficiency in using tools such as Scifinder, Reaxys for literature search, able to read and design/optimize synthesis routes based on English literature.
  5. Strong hands-on experimental skills in organic synthesis, capable of reproducing experiments from literature.
  6. Attention to detail, ability to identify and logically solve problems.
  7. Adherence to standard laboratory practices and good experimental habits. Accurate, complete, clear, and timely documentation of experiments.
  8. Excellent communication skills and ability to work in a team.

Responsibilities:

  1. Participate in the design and modification of target molecules according to company strategic goals.
  2. Conduct literature reviews, design experimental plans and synthesis routes, and formulate project plans.
  3. Develop feasible experimental plans, lead 1-3 staff members in experiments, and efficiently obtain target compounds.
  4. Communicate promptly with relevant departments, assisting in project coordination to ensure overall project progress.
  5. Proactively communicate technical issues with team leaders, actively discuss solutions, and ultimately resolve problems.
  6. Execute laboratory management practices to ensure compliance with company EHS, quality standards, technical confidentiality, and regulatory requirements.
  7. Accurately, completely, clearly, and timely complete experimental records and project reports.
Apply
Clinical Research Associate

Qualifications:

  1. Bachelor's degree or above in Clinical Pharmacy, Medicine, or Nursing; with 2+ years of work experience.
  2. Familiarity with clinical trial management regulations and the entire drug development process.
  3. Clear written and verbal communication skills, adept at communication.
  4. Excellent teamwork skills; able to adapt to frequent travel and high work pressure.

Responsibilities:

  1. Conduct central screening and center qualification before the start of clinical trials.
  2. Responsible for monitoring Phase I to IV clinical trials, and preparing trial-related documents as required.
  3. Conduct comprehensive monitoring and management of assigned research centers according to the protocol, SOP, and GCP.
  4. Complete the start-up, execution, and closure of clinical trials at the center on time.
  5. Report trial progress monthly or as required, and communicate problems encountered with the Project Manager.
Apply
Clinical Pharmacology Manager

Qualifications:

  1. Master's degree or above in Clinical Pharmacology, Pharmacokinetics, or related fields, with more than 3 years of experience in the design and development of clinical pharmacology for biologics.
  2. Background in DMPK, biology, pharmacology, and clinical research; familiarity with CFDA/FDA/EMA regulations; proficient in writing clinical trial protocols and summary reports.
  3. Strong ability in literature reading and information retrieval.
  4. Diligent, proactive, strong learning ability, with good teamwork and communication skills.

Responsibilities:

  1. Design and write early clinical trial protocols and reports, including PK/PD, PPK, PBPK, etc.
  2. Write Phase I study protocols and summary reports, and the clinical pharmacology section of Phase II/III clinical trials.
  3. Write investigator's brochures and the clinical pharmacology section of IND/NDA submission documents.
  4. Responsible for clinical pharmacology-related data statistics and analysis, including PK and PK/PD analysis.
  5. Communicate with clinical pharmacology experts to ensure the scientific and implementable design of protocol-related content.
  6. Assist in the bidding process for clinical trial design and provide output for clinical research proposals and other core research.
Apply
Pharmacovigilance Manager

Qualifications:

  1. Master's degree or above in Medicine or Pharmacy.
  2. Over 3 years of experience in clinical drug safety management in pharmaceutical companies or CROs.
  3. Familiar with adverse reaction related systems such as Arisg, Argus, common EDC, etc.
  4. Understanding of drug and medical device registration methods, adverse event reporting and detection, familiarity with GVP and other regulations.
  5. Basic English skills, capable of translating adverse events between Chinese and English.
  6. Good communication, strong learning ability, execution, and some project management skills.

Responsibilities:

  1. Responsible for drug safety work, drafting work plans and plans according to industry regulatory requirements, and organizing implementation.
  2. Responsible for establishing work standards and processes, and establishing a sound drug safety work system and mechanism.
  3. Collect, organize, analyze, and report serious adverse reactions (SAE) or unexpected adverse events during clinical trials.
  4. Ensure effective implementation of SAE/unexpected adverse event tracking and reporting work in strict accordance with regulatory requirements and company regulations.
  5. Maintain smooth communication channels with relevant regulatory departments and business partners to ensure smooth drug safety communication.
Apply
Senior Clinical Data Management Manager

Qualifications:

  1. Over 3 years of experience in clinical trial data management in pharmaceutical companies, familiar with the main processes and principles of new drug clinical trial data management, with experience in establishing EDC clinical trial databases, data auditing, and cleaning.
  2. Master's degree or above in Medicine, Health, Clinical, Nursing, Information/Computer Science, or related fields.
  3. Understanding of "Drug Administration Law," "Regulations for Drug Approval," knowledge of ICH-GCP, understanding of the entire drug development process, familiarity with the entire process of clinical trials and data management.
  4. Proficient in English listening, speaking, reading, and writing, willing to learn, good learning ability, and proactive.

Responsibilities:

  1. Overall responsibility for all activities and progress tracking of clinical trial data management, quality control.
  2. Provide data management advice on clinical trial protocols; assist in the formulation and finalization of CRF and CRF audit.
  3. Responsible for communication, coordination, and management of third-party data companies, review data management-related documents provided by data providers, such as data management plans, data verification plans, CRF completion guidelines, external data transfer protocols, SAE consistency comparison plans, data management reports, etc.
  4. Audit and test EDC systems; regularly review EDC data, record, track, communicate, and resolve problems or risks discovered; responsible for supervising database lock.
  5. Participate in clinical trial protocol discussions, project discussions, summaries, etc.
  6. Establish and improve clinical trial data management quality management system documents.
Apply