Accountable for clinical evidence strategy development, delivery & dissemination for HPM products throughout the entire product creation and lifecycle to deliver evidence of value.
This role is mainly responsible for the maintenance and management of team regulations and clinical databases, as well as the collection and compilation of clinical evidence of standard compliance. Support the retrieval and screening of clinical literature and PMS data.
Complete the following contents according to the requirements：
1. Manage and maintain the team's clinical evidence database.
2. Regularly collect clinical related regulations, standards and guidelines, manage the team's regulatory database.
3. Collect clinical evidence and complete the human clinical confirmation report meeting the standard requirements according to the standard requirements.
4. Support the retrieval and screening of clinical literature and PMS data.
1.Prefer sophomore, junior, first-year graduate student or second-year graduate student. Can work in different places
2.major in clinical medicine, biomedical engineering, biostatistics, clinical nursing.
3.mandatory technical skills: Basic English skill& amp; Good computer skill.