Seeking a Clinical APM/PM talent for insuring clinical trial projects. The position will be responsible for certain clinical trials management. This individual ensures that clinical

trials are executed according to ICH/GCP/NMPA/FDA/CDE guidelines, applicable regulatory requirements, and company’s standard operating procedures.

Key Accountabilities:

Assist in formulating clinical project plans, including project timeline, budget plans,

monitoring plans, communication plans, risk management plans, training plans, and quality control plans.

Be responsible for reviewing and organizing ethical documents submissions.

Be responsible for the project overall progress following-up and communication.

Reasonably allocate work and resources for CRA according to the needs of clinical trials.

Responsible for supplier selection, cooperation communication, and payment follow-up.

Organize and coordinate researchers’ meetings.

Assist in medical review, such as reviewing protocols, informed consent forms, case report forms, etc.

Qualifications:

Bachelor's degree or above, with major in medicine, pharmacy, or related fields.

Having at least 4 years’ experience of Lead CRA or project management fields from Multi- National Corporation.

Strong interpersonal skills commensurate with the need to work closely with CROs, researchers, and team members across functions.

Ability to thrive in a fast-paced environment.

Able to manage multiple tasks and prioritize accordingly.

Exceptional written and oral English skills to meet the needs of clinical trials routine work.

Possess the ability to independently analyze and solve problems, as well as the ability to learn quickly.