CAREERS

Research Scientist

 

We are currently seeking a highly talented and motivated Research Scientist to join our Research and Development team. The ideal candidate will have a strong passion and curiosity for development and applications of new biologics to address unmet medical needs. The successful candidate will be responsible for research and development of novel vaccine and antibody platforms based on our patented technologies to prevent and treat infectious diseases and cancers.

Reporting to the R&D director, the appointee will be required to:

  • Lead and manage a translational research project to meet project goals
  • Design and conduct rational experimental studies to develop and validate new biologics products
  • Perform data analysis and interpret results from experiments independently
  • Keep proper records of all experimental work and data generated
  • Participate in the preparation of grant applications and publications
  • Prepare standard operating procedures, study protocols, and reports as necessary
  • Communicate effectively and timely with the management team about experimental results and scientific literature
  • Supervise and provide training to junior staff
  • Perform any other duties as assigned

 

Requirements:

  • A recognized PhD degree in Biomedical Sciences, Immunology, Virology, Biotechnology, Biochemical, or other science / medical related disciplines
  • At least 3 years of relevant experience in translational research projects
  • Fresh PhD graduates are welcome
  • Familiar with basic techniques, including molecular cloning, cell culturing, ELISA, flow cytometry, etc
  • Experience in project design and team management would be an advantage
  • Possess a can-do attitude, be prepared to think and work outside the box, and be willing to learn
  • Be a good team player with excellent interpersonal, presentation and project management skills
  • Be fluent in written and spoken English and Chinese, including Putonghua.

 

Benefit:

  • 5 working days
  • Annual leave 16 - 18
  • Birthday leave
  • Medical insurance
  • Performance bonus
  • ESOP

 

Salary: $32,000+; Would be set according to the applicants’ qualifications and experience.

 


 

Associate Scientist

 

We are currently seeking several highly motivated Associate Scientists to join our Research and Development team. The successful candidates will participate in high quality research to develop and validate new therapeutics for unmet medical needs.

Reporting to the R&D director, the appointees will be required to: 

  • Conduct basic molecular and immunological assays
  • Properly record all experimental procedures and data generated
  • Assist in daily laboratory operations, such as reagent preparation, ordering, and equipment maintenance
  • Carry out any other duties as assigned

 

Requirements:

  • Diploma / Associate Degree / bachelor's or master's degree in Biochemistry, biotechnology or relevant fields
  • Fresh graduates are welcome
  • Experience in basic molecular and cell culture techniques would be preferred
  • Working experience in pharmaceutical, biotech, or other related research settings would be an advantage  
  • Able to work independently, adaptable, detail-oriented, with a strong sense of responsibility and organizational ability
  • Good command of English and Chinese (proficiency in Putonghua an advantage)

 

Benefit:

  • 5 working days
  • Annual leave 14 - 18
  • Birthday leave
  • Medical insurance
  • Performance bonus
  • ESOP

 

Salary would be set according to the applicants’ qualifications and experience.

 


 

Senior Clinical Research Associate / Clinical Research Specialist

 

Responsibilities:

  • To participate in design, prepare, apply and monitor the phase 1, 2 and 3 clinical trial studies in HK, the Mainland and Overseas.
  • To assist the preparation of Clinical trial protocol and Investigational Brochure and other related technical documents.
  • To work with the CRO, Clinical Trial Centers and Principle Investigators to manage and control the clinical trial studies complying with the requirements of the regulatory authorities.
  • To work with various teams, like R&D, manufacturing development team, regulatory affairs and management, on all clinical trial related activities.
  • Provide opinions and inputs on medical and potential safety issues of clinical trials as assigned.
  • Conduct medical and safety monitoring during the clinical trials studies
  • Occasionally travel to the Mainland or overseas is required.

 

Requirements:

  • A bachelor's or master's degree from a local university or a Doctor's degree from a local university or a well-known non-local institution in clinical, healthcare, pharmacy, or other related science and medical subjects.
  • Solid experience in clinical trial center or hospitals, to handle preclinical or clinical studies is preferred.
  • At least 2 years hand-on experience in clinical trial preparation and management, such as, clinical trial design and setup, clinical trial monitoring, reporting, data interpretation and publications.
  • Able to work independently, adaptable, detail-oriented, with a strong sense of responsibility and organizational ability.
  • Good command of English and Chinese (proficiency in Putonghua is an advantage).

 

Benefit:

  • 5 working days
  • Annual leave 16 - 18
  • Birthday leave
  • Medical insurance
  • Performance bonus
  • ESOP

 

Salary would be set according to the applicants’ qualifications and experience.

 


 

Senior Regulatory Affairs Officer / Regulatory Affairs Specialist

 

Responsibilities:

  • To work with and support technical team to prepare, review and summarize the information, results and records during research, preclinical studies and clinical studies for IND submission of biologics products in the Mainland, HK and Overseas.
  • To work with CRO team and internal teams to fulfill the regulatory requirements during the IND and Clinical trial application and approval process in the Mainland, HK and Overseas.
  • To assist other technical teams on the preparation of documents to fulfill the regulatory requirements.
  • To participate the communication and build closed working relationship with regulatory authorities.
  • To handle other activities related to regulatory affairs/product registration issues.
  • Maintain and update the documents to fulfill the latest regulations and related information.
  • Occasionally travel to the Mainland or overseas is required.

 

Requirements:

  • A bachelor's or master's degree from a local university or a Doctor's degree from a local university or a well-known non-local institution.
  • Biochemistry, biotechnology or other science or medical related specialties.
  • At least 2 years regulatory affairs experience in pharmaceutical, biotech fields; GMP experience is an advantage.
  • Able to work independently, adaptable, detail-oriented, with a strong sense of responsibility and organizational ability.
  • Good command of English and Chinese (proficiency in Putonghua is an advantage

 

Benefit:

  • 5 working days
  • Annual leave 16 - 18
  • Birthday leave
  • Medical insurance
  • Performance bonus
  • ESOP

 

Salary would be set according to the applicants’ qualifications and experience.

 


 

Senior Quality Management Officer / Quality Management Specialist

 

Responsibilities: 

  • Participate in design and monitoring of stability studies experiments of newly developed biologics products;
  • Review and provide quality and compliance related inputs for test methodology development and verification; manufacturing process development, improvement and scale-up; technology transfer projects;
  • Supports and participate in other product performance related studies and tests.
  • Work with technical team in manufacturer to establish of product quality analysis system, including raw materials, intermediate products, and finished products.
  • To participate in and work with quality and engineering teams to establish validation plan, on equipment, facility, manufacturing and testing process etc.
  • Participate in the review of documentation, policies, protocols and reports, to ensure the compliance of GMP and regulatory requirements.
  • Conduct quality inspection and audit of the manufacturer, research institutions, animal test centers and other product efficacy, quality and safety related test centers.
  • Provide quality and compliance related inputs on technical contacts and agreements signed with external parties.
  • Occasionally travel to the Mainland or overseas is required.

 

Requirements: 

  • A bachelor's or master's degree from a local university or a Doctor's degree from a local university or a well-known non-local institution in biochemistry, biotechnology, pharmacy or other science and medical related area.
  • At least 2 years of QA/QC experience in pharmaceutical / biotech industry with GMP accreditations.
  • Independent, detail minded, with good communication skills and ability to interact with people at all levels.
  • Good command of English and Chinese (proficiency in Putonghua is an advantage).

 

Benefit:

  • 5 working days
  • Annual leave 16 - 18
  • Birthday leave
  • Medical insurance
  • Performance bonus
  • ESOP

 

Salary would be set according to the applicants’ qualifications and experience.

 


 

Project Manager

 

We are currently seeking a highly talented and motivated Project Manager to join our Research and Development team. The ideal candidate will have a strong passion and curiosity for development and applications of new biologics to address unmet medical needs. The successful candidate will be responsible for research and development of novel vaccine and antibody platforms based on our patented technologies to prevent and treat infectious diseases and cancers.

 

Roles and Responsibilities:

  • Assist in the application of research grant proposal
  • Provide support including communication, administration, logistics and ethics compliance process of clinical trials throughout the project life cycles
  • Provide support to the R&D team to conduct translational research projects
  • Liaise with internal and external parties to ensure the projects (e.g., R&D, clinical trials, collaboration) are carried out in a timely manner;
  • Ability to manage multi-projects independently and under tight timelines.
  • Prepare reports for grant committee and management team
  • Manage website and social media channel if needed;
  • Perform other tasks as assigned.

 

Requirements

  • Master degree/ PhD degree in Molecular Biology/ Virology/ Biomedical Sciences/ Biochemistry/ Biology or a related science disciplines;
  • Strong project management skills with the ability to manage stakeholder expectations with both internal and external parties;
  • Experience in the application of research grant proposal is an advantage;
  • Working experience in coordinating clinical trial is preferable;
  • The ability to work independently with minimal supervision
  • A mature work attitude with good communication and interpersonal skills;
  • Working experience in communication is advantages. 

 

Benefit:

  • 5 working days
  • Annual leave 16 - 18
  • Birthday leave
  • Medical insurance
  • Performance bonus
  • ESOP

 

Salary would be set according to the applicants’ qualifications and experience.

 

Applicant can submit your up-to-date C.V., quoting the position, current/expected remuneration and availability to hr@immunocure.hk