北京招聘

Ensure successful clinical trial startup and conduction, accountable for all study aspects and ensuring meeting timeline, budget and quality requirement.

1. Support IND filing on study related documents preparation, e.g. protocol, ICF, IB etc.
2. Manage study planning and startup all activities including not limited to country/site selection, EC/HGRAC submission, study TMF preparation, vendor/system set-up, Clinical trial materials planning and readiness at depot, study plan development etc.
3. Manage trial enrollment and monitor overall progress, make mitigation/action plans and execute ensuring enrollment hit target.
4. If applicable, lead I-Mab functional team on CRO selection, manage and monitor performance of all CROs ensure delivering on time and high quality.
5. Manage various of clinical vendors contract and overseeing their performance.
6. Have responsibility for the financial management of the clinical trial including budget planning, resource allocation and preparation of quarterly reports.
7. Train and coach CRAs in various aspects of management (e.g. HR, budgets, resource allocation) that are relevant to project issues.
8. Work as product level project team member and contribute from clin. Ops perspective.
9. Identify/monitor risks, and develop mitigation, contingency plans as necessary.

Qualifications:

1. Bachelor’s degree and above.
2. Major in clinical medicine, pharmacy and biology or relevant.
3. Experienced in clinical trial area and preference on: >6 years clinical trial related experience & >3 years trial management for PM；Previously worked in global pharma or CRO and/or early development functions.
4. Knowledgeable to China regulatory and clinical requirements, with experience of interacting with regulatory agencies, e.g. CDE, HGRAC, CFDI.
5. Solid understanding of GCP and Drug development.
6. Ability to work independently and collaborate.
7. Strong communication skills and leadership.
8. Strong oral and written communication skills in Chinese and English.