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.

QuintilesIMS pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow us to create more effective trials and determine outcomes faster.
 
If that is your passion, we have a place for you.