北京招聘

PURPOSE

Provide project related assistance for assigned complex project(s), sites and project teams. Lead teams functionally, where assigned, including awareness of scope of work, budget, and resources. Ensure all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements and meets quality and timeline metrics.

 

RESPONSIBILITIES

Perform complex processes and tasks that eventually result in high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines

Establish and maintain effective project/ site communications

Create and maintain relevant project documents

Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information

Review, evaluate and recommend modifications to designated processes

Participate in document management (creation, review, maintenance, storage, as applicable)

Participate in (study) team meetings and implement action items

Collaborate with the project lead/team members in creation/review of study documents

Setting quality standards and reviewing deliverables to the same for process tasks.

 

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

Good knowledge of, and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines

Strong written and verbal communication skills including good command of English language

Results and detail-oriented approach to work delivery and output

Good problem solving skills

Good planning, time management and prioritization skills

Ability to handle conflicting priorities

Attention to detail and accuracy in work

Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint

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

Proven ability to work on multiple projects balancing competing priorities

Good leadership skills

Ability to work across cultures and geographies with a high awareness and understanding of cultural differences

Setting quality standards and reviewing deliverables to the same for process tasks.

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

Bachelor's degree in life sciences or related field and min 3 years relevant experience; or equivalent combination of education, training and experience

 

PHYSICAL REQUIREMENTS

Extensive use of keyboard requiring repetitive motion of fingers.

Extensive use of telephone and face-to-face communication requiring accurate perception of speech.

Regular sitting for extended periods of time.

May require working in shifts.

IQVIA（纽交所代码：IQV）是全球专注生命科学领域的高阶分析、技术解决方案和临床研究服务供应商。IQVIA利用深入分析、前沿技术、大数据资源和广泛领域的专业知识，智能连接医疗生态的各个环节。IQVIA Connected Intelligence？快速敏锐地为客户提供强大的数据洞察，帮助客户加速创新医疗的临床开发和商业化进程，以更好的医疗成果惠及患者。IQVIA拥有约72,000名员工，足迹遍布100多个国家/地区。

IQVIA拥有多元化的加强型隐私技术和保障手段，能够在保护个人隐私的同时对信息进行管理和分析，帮助医疗利益相关方有效开展精准疗法，获得更佳的疗效。这些洞见和能力能够帮助生物科技、医疗器械、制药公司、医学研究者、政府机关、支付方以及其他医疗利益相关方，获得对疾病、人类行为和科技进步更深入的理解，共同朝着治愈各类疾病的方向迈进。