Corporate Value
Careers
Provide A Good Career
Development Platform
for Employees
Development Platform
for Employees
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OpenWe stay open-minded to new ideas with creativity and innovation.
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ViableWe make remitting efforts to transform scientific research into commercial viability.
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HumbleWe are humble about science, technology, nature, and people.
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UnitedWe work together as a united team with trust and respect.
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BreakthroughWe devote ourselves to delivering breakthrough therapies for clinical benefits.
Why Immvira
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Competitive CompensationOur people are our greatest asset.We make every effort to provide essential and desirable benefits that make each employee's life that much easier. We also offer competitive compensation that rewards you for your contributions toward achieving company goals.
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Flexible Working EnvironmentWe value fostering a healthy, creative and diversified work culture that motivates our employees. Our company embraces a flat hierarchy regardless of seniority. We believe in having fun while creating quality work, and enjoy taking time together to re-energize.
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Friendly and Supportive TeamWe are willing to take risks, to learn, and to grow together. If you are looking for a dynamic and collaborative team, come and join us to unleash the potential of cutting-edge technology and make your unique mark on the future of human health.
Join Us
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Beijing. Suzhou. Hefei. Shenzhen2022-09-27Learn MoreClinical Supervisor
1.Screening and initiation of study centers.
2.Provide ongoing training to center personnel on GCP, study protocols and requirements.
3.Collect necessary documentation and update investigator folders and TMF in a timely manner according to protocol and regulatory requirements during the initiation and completion phases of the study.
4.Perform clinical monitoring according to company SOPs and manage the entire process of clinical trials.
5.Ensure that the trial is conducted in strict accordance with the protocol, GCP and relevant laws and regulations.
6.Assist in solving any problems that may arise during the trial.
7.Ensure the study data is timely. Accuracy. Integrity.
8.Responsible for the operation and execution of clinical projects according to the project plan and schedule to ensure that clinical projects are completed as required.
9.Assist in organizing various meetings related to clinical trials and maintain good communication and coordination with research units and experts.
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Shenzhen China2022-09-27Learn MorePharmacology and Toxicology Researcher
1.Responsible for the preclinical pharmacodynamics of new drug development, Toxicology and pharmacokinetics and other related data collation, the development of new drug development pharmacology and toxicology development program, participate in animal testing in animal centers.
2.Responsible for CRO research, implementation of relevant research, tracking the progress of the trial, and analysis and summary of the trial results.
3.Responsible for the study protocol. Review and approval of study protocols, summary reports and other related technical information.
4.Responsible for the translation and writing of the pharmacology and toxicology part of the new drug application materials, and cooperate with the registration, CMC and clinical staff to complete the work related to the new drug application.
