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Business Development
3-5 years
Undergraduate
Nanjing
2025-02-28
Job Description:
1. Achieve assigned sales targets from direct leadership in alignment with the company's overall business strategy.
2. Monitor market intelligence and industry trends to identify and secure beneficial partnership opportunities for the company.
3. Execute defined business development strategies and plans: conduct client visits, understand client needs, promote relevant services, lead business negotiations, and finalize partnership evaluations and contract execution.
Business Focus Areas:
1. Preclinical studies for novel drugs
2. Clinical Research (Bioequivalence (BE) + Confirmatory Clinical Trials)
3. Custom Chemical Synthesis (CCS)
Qualifications & Requirements:
1. Bachelor's degree or higher in Biomedical Sciences, Pharmaceutical Sciences, or a related discipline.
2. Minimum 3 years of relevant experience in R&D, marketing, or business development within pharmaceutical, biotechnology, or CRO companies is preferred.
3. Demonstrated execution capability, strong business negotiation skills, and excellent team collaboration. Possesses an international perspective and professional acumen within the field.
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Advanced Formulation Project Manager
5-10 years
Undergraduate
Nanjing
2026-04-01
Job Responsibilities:
1. Track trends in formulation technology research and technology market developments to support formulation design and development for projects.
2. Independently conduct literature review, formulation screening, process development, stability studies, and scale-up to ensure smooth project execution.
3. Conduct research in compliance with requirements, properly maintain raw records and organized documentation, and draft study reports and relevant regulatory submission materials.
Qualifications:
1. Bachelor's degree or above in Pharmacy, Pharmaceutics, Pharmaceutical Engineering, or a related field.
2. At least 5 years of experience in pharmaceutical formulation R&D, with demonstrated technical expertise in the development of relevant dosage forms.
Based in:
Nanjing
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Topical Formulation Project Manager
Morethan3 years
Undergraduate
Nanjing
2026-04-01
Job Responsibilities:
1. Independently lead a team in the development of topical semi-solid formulations (e.g., ointments, gels, creams), covering literature review, formulation screening, process development, stability studies, and scale-up, ensuring smooth project execution.
2. Develop and implement formulation development plans, track project progress, and promptly analyze and resolve technical issues encountered during R&D to ensure timely, high-quality project delivery.
3. Independently or by guiding the team, draft relevant pharmaceutical study documents, raw data records, and CTD-format submission materials to ensure compliance with regulatory requirements.
4. Communicate with clients regarding assigned projects to jointly advance the submission process.
Qualifications:
1. Bachelor’s degree or above in Pharmacy, Pharmaceutics, Pharmaceutical Engineering, or a related field.
2. At least 3 years of R&D experience in topical semi-solid formulations with a proven track record of successful regulatory approval.
Based in：
Nanjing
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CRA
1-3 years
Undergraduate
Nanjing
2026-03-20
Job Responsibilities:
1. Responsible for clinical trial monitoring, ensuring that all trials are strictly conducted in accordance with the clinical trial protocol, standard operating procedures/internal operating procedures, and applicable regulations.
2. Perform comprehensive monitoring and liaison management for assigned study sites, completing the initiation, execution, and closure of clinical trials at these sites on time.
3. Develop monitoring plans and prepare monitoring reports to ensure clinical research progresses according to schedule.
4. Assist senior supervisors in selecting trial sites for assigned projects and controlling trial budgets.
5. Serve as an external representative of the company and clients, effectively communicating important company and client information to investigators (physicians), and fostering and maintaining good relationships with them.
Job Requirements:
1. Bachelor's degree or above in medicine, pharmacy, or related fields.
2. More than two years of experience in a similar role.
3. Responsible, diligent, grounded, and proactive.
4. Strong learning ability and execution capability.
Based in:
Nanjing, Lianyungang, Zhengzhou, Lishui, Wuhan, Tianjin, Jinan
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PM
Morethan3 years
Undergraduate
Nanjing
2026-03-20
Job Responsibilities:
1. Responsible for the project management of various clinical trials conducted by the company, providing comprehensive quality control and progress management for the assigned clinical research projects, ensuring that all trials are strictly conducted in accordance with GCP, SOPs, study protocols, and Chinese laws and regulations.
2. Develop a project management plan based on the contract requirements and clinical trial protocol, defining the scope of responsibilities, team members, progress schedule, financial budget, etc., and continuously review and revise the project management plan as the project progresses.
3. Regularly report on the trial progress according to the contract and submit project progress reports.
4. Review and approve the actual working hours and expenses incurred by project team members during project implementation in accordance with the contract and project plan, ensuring that all tasks are completed within the timeframe and budget agreed upon with the client.
5. Supervise project team members to complete the overall initiation, execution, and closure of clinical trials on time for the assigned projects.
6. Conduct site co-visits for the assigned clinical trials as required by the contract and when necessary, and complete site co-visit reports.
7. Identify, monitor, and promptly address various risks throughout the project, accurately assess the overall impact of corresponding risks on the project, and implement reasonable improvement measures.
8. Ensure the completeness, accuracy, and timeliness of clinical trial project documentation.
9. Serve as the primary liaison for clinical trial projects, representing the company and project team in maintaining timely and effective communication with sponsors, principal investigators, and vendors, ensuring that key project information is accurately and completely conveyed, and fostering and maintaining good relationships with study sites and clients.
10. Handle emergencies in the project promptly and provide training to project team members.
11. Communicate and coordinate with various functional teams regarding the assigned research projects, such as medical writing, data and statistics, and quality assurance personnel.
Job Requirements:
1. Bachelor's degree or above in medicine, pharmacy, or related fields.
2. At least 3 years of CRA experience and 1 year of APM experience.
3. Familiarity with GCP and the phases and requirements of clinical research.
4. Ability to lead a team, with strong interpersonal skills and the capability to coordinate and collaborate across departments.
5. Proficiency in using office software.
Based in:
Nanjing
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