您将获得的技能: Chemistry, Natural Resource Management, Food and Beverage, Biochemistry, Environment and Resource Management, Chemical Engineering, Pharmaceuticals, Materials science, Nutrition and Diet, Analytical Chemistry, Laboratory Procedures

您将获得的技能: Pharmacology, Drug Development, Clinical Trials, Clinical Research, Pharmaceuticals, Pre-Clinical Development, Infectious Diseases, Patient-centered Care, New Product Development, Medical Science and Research, Informed Consent

您将获得的技能: Good Clinical Practices (GCP), Clinical Research, Clinical Trials, Clinical Research Ethics, Informed Consent, Clinical Data Management, Institutional Review Board (IRB), Patient Education And Counseling, Drug Development, Health Equity, Risk Management

您将获得的技能: Google 云端平台, 非结构化数据, 数据处理, 文本挖掘, 临床信息学, 健康信息学, R 语言程序设计（中文版）, 临床文件, 自然语言处理

您将获得的技能: 回归分析, 机器学习算法, 数据操作, 机器学习, 预测建模, 分子生物学, Pandas（Python 软件包）, 深度学习, 探索性数据分析, 降维, Scikit-learn （机器学习库）, 药物开发, 应用机器学习, 功能工程, 无监督学习, 生物信息学, 人工神经网络

您将获得的技能: 禁忌症, 临床评估, 实验室测试, 社区卫生, 血源性病原体, 药物相互作用, 初级保健, 病人沟通, 健康差异, 患者评估, 公共卫生, 诊断测试, 病人教育与咨询, 预防保健, 患者宣传, 药理学, 健康公平, 药物治疗管理, 药物疗法

您将获得的技能: 生物学, 肿瘤学, 心理健康疾病与障碍, 古代历史, 药物相互作用, 患者安全, 疼痛管理, 化学, 世界历史, 临床试验, 医疗保健伦理, 精神病学, 神经学, 药理学, 药物滥用, 生理学

您将获得的技能: Medical Prescription, Drug Interaction, Pharmacotherapy, Medication Administration, Medication Dispensation, Pharmacology, Patient Safety, Patient Education And Counseling, Health Care, Geriatrics

您将获得的技能: Drug Interaction, Pharmacology, Pharmacotherapy, Dentistry, Dental Care, Contraindication, Medication Therapy Management, Pharmaceuticals, Oral Health, Pain Management

您将获得的技能: 医疗程序和 Regulator, 禁忌症, 病人沟通, 慢性疾病, 疼痛管理, 一般科学与研究, 患者安全, 药物相互作用, 护士教育, 患者评估, 病人教育与咨询, 呼吸护理, 妇科, 医学科学与研究, 药理学, 医疗保健行业知识, 健康与安全标准, 药物疗法, 药物治疗管理, 药品

您将获得的技能: Good Clinical Practices (GCP), Institutional Review Board (IRB), Clinical Research Ethics, Clinical Research Coordination, Clinical Trials, Clinical Research, Drug Development, Informed Consent, Document Management, Electronic Medical Record

您将获得的技能: Good Clinical Practices (GCP), Informed Consent, Clinical Research, Clinical Trials, Clinical Research Ethics, Institutional Review Board (IRB), Drug Development, Record Keeping, Clinical Documentation, Regulatory Compliance, Patient Communication