Careers
Epigenic Therapeutics，looking forward to your joining！
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MedicineOcular Scientist
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Number of recruits：1
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Place of work：Shanghai
Responsibilities:
1.Mainly engaged in the research and development of pharmacological effects of eye diseases, including in vivo drug metabolism, efficacy evaluation, and early toxicological evaluation.
2.Proficiency in ophthalmology-related experimental procedures, including: construction of animal models of ophthalmic diseases, subretinal injection, intravitreal injection, tissue sectioning, immunofluorescence staining, etc.
3.Work with relevant responsible persons to complete the formulation and progress tracking of relevant research plans, data analysis, etc.
4.Make experimental records according to regulations, promptly organize experimental results, and report project progress to relevant responsible persons;
Qualifications:
1.Master's degree or above in biology or medicine related majors, with 2-3 years of experience in ophthalmic diseases;
2.Familiar with ophthalmology-related experimental techniques and have a deep scientific understanding of eye development or ophthalmic diseases;
3.With the ability to independently analyze and solve problems, possessing strong comprehension and interpersonal skills, and exhibiting a team spirit;
4.Familiar with office software such as Prism, ImageJ, Adobe Illustrator, etc., with a high level of English literature reading ability.
5.Have good conduct, hard work, strong sense of responsibility, and work carefully and conscientiously;
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MedicineCRA（Clinical Research Associate）
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Number of recruits：1
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Place of work：Shanghai
Responsibilities:
1.Be responsible for the specific implementation and monitoring of clinical trials, ensuring that projects are conducted in accordance with national GCP requirements, trial protocols, and company standard operating procedures, and implementing quality control throughout the entire process.
2.Conduct comprehensive management of the assigned research centers, strictly adhering to GCP, SOP, trial protocols, and Chinese laws and regulations, and timely and completely complete the selection, initiation, routine monitoring, and closure of research centers within the project timeline.
3.Coordinate communication and collaboration with various parties involved in the trial, such as medical institutions, ethics committees, and subjects.
4.Monitor the progress of the trial, ensure that it proceeds as planned, and promptly address any issues that arise during the trial.
5.Review and organize trial documentation, including trial records, subject data, trial reports, etc., to ensure their completeness and accuracy.
6.Participate in the initiation, execution, and closure of clinical trials to ensure their smooth progress and high-quality completion.
7.Maintain close communication with the research team, provide necessary support and suggestions, and ensure the achievement of trial objectives.
8.Comply with relevant laws, regulations, and industry standards to ensure the compliance of the trial.
Qualifications:
1.Bachelor's degree or above in biomedicine, clinical medicine, pharmacy, or related fields, with professional knowledge in relevant areas.
2.More than three years of work experience as a CRA or in related fields, with a good understanding of GCP and relevant regulatory requirements.
3.Possess good communication and coordination skills, able to effectively collaborate with multiple parties.
4..Have strong problem-solving and analytical skills, capable of addressing various challenges during the trial.
5.Have good document management and organizational skills to ensure the completeness and accuracy of trial documentation.
6.Possess good teamwork spirit and professional ethics, able to withstand work pressure and maintain a positive attitude.
7.Excellent English listening, speaking, reading, and writing skills, able to read and understand English literature and documentation.
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