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JOIN US! Adicet Bio, Inc. is a clinical stage biotechnology company discovering and developing allogeneic gamma delta T cell therapies for autoimmune diseases and cancer. Adicet is advancing a pipeline of “off-the-shelf” gamma delta T cells, engineered with chimeric antigen receptors (CARs), to facilitate durable activity in patients. For more information, please visit our website at  https://www.adicetbio.com . Shanghai Adicet Biotechnology Co., Ltd. is a clinical stage biotechnology company developing allogeneic gamma delta T cell therapies for autoimmune diseases and cancer. Shanghai Adicet is advancing a pipeline of “off-the-shelf” gamma delta T cells, engineered with chimeric antigen receptors (CARs), to facilitate durable activity in patients. The pipeline developed by Shanghai Adicet was discovered and is being developed outside of China by Adicet Bio, please visit https://www.adicetbio.com for additional details on the pipeline.  Onsite in Shanghai, China Clinical Trial Manager (CTM) We are seeking a highly motivated and experienced Clinical Trial Manager (CTM) to join our dynamic China clinical operations team. This role is critical for the successful execution of our international Phase I/II clinical trials in China. The ideal candidate will be a hands-on professional who thrives in a fast-paced, global biotech environment. You will serve as the key person to oversee local vendors, ensuring seamless study implementation and delivery.   Key Responsibilities: Global Study Execution: As the local CTM to collaborate with US Headquarter to implementation of global Phase I/II clinical trials in China, ensuring compliance with the global study protocol, ICH-GCP, and local regulatory requirements. May serve as an independent CTM to manage China standalone trials. Vendor Management: Select, manage, and oversee local vendors, including CROs, SMOs, and Investigational Product (IP) depots, to ensure high-quality delivery within agreed timelines and budgets. Cross-Functional Collaboration: Work closely with the US-based global study team, contributing to study planning and providing timely updates on China-specific progress, challenges, and risks. Site Management: Collaborate with key site staff to facilitate site initiation, patient recruitment, data quality, and overall site performance. Budget and Timeline Management: Manage the local country budget and ensure study milestones are met. Proactively identify and mitigate risks to the study timeline. Quality and Compliance: Ensure all clinical activities adhere to standard operating procedures (SOPs), GCP, and applicable regulations. Lead or contribute to internal and vendor audits/inspections as needed. Problem Solving: Quickly identify issues and implement effective, practical solutions to keep the study on track.   Qualifications and Experience Education: Bachelor’s degree or higher in a life sciences or related field Experience: 1-3 years of direct, hands-on experience in clinical operations within the pharmaceutical industry, with a proven track record of managing clinical trials in China. Therapeutic Area: Strong experience in Oncology and/or Autoimmune Diseases is highly preferred. Trial Phase Expertise: Practical experience managing Phase I and/or Phase II clinical trials are highly preferred. Biotech Background: Prior experience working in a biotech or small-to-mid-size pharmaceutical company is strongly preferred, with an appreciation for the agile and hands-on culture. Vendor Management: Demonstrated success in managing and overseeing CROs and other third-party vendors. Language Skills: Fluent in English and Mandarin, with excellent verbal and written communication skills.       Pay Range $150,000 — $190,000 USD Adicet fosters a collaborative, high-performing environment by p