Job Responsibilities

1. Develop, maintain, and oversee the clinical trial to ensure the quality management.

2. Ensure that clinical trial compliance with the policies, protocol, schedule and SOP.

3. Monitor project scope, schedule and costs to ensure all remain on track per contract.

4. Build required project plans, and per SOPs, implement and monitor progress against project plans revising as necessary.

5. Work with CRO and others closely to solve problems from clinical trial.

6. Develop and maintain professional relationship with leading PIs and external investigators.

Job Qualifications

1. B.S. degree or above in clinical medicine, pharmaceutical science or related fields. Experience managing clinical trials from start to finish.

2. Basic drug R&D, therapeutic and protocol knowledge. Understanding of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

3. Strong communication and interpersonal skills. Excellent problem-solving skills.

4. Ability to establish and maintain effective working relationships with coworkers, managers and clients.

5. Fluency in oral and written English.

6. 2 years’ experience in clinical project management experience is preferred.

Location: Shanghai

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