Clinical Analyst- CA - (1627076) in Beijing, CN at IQVIA™

Date Posted: 5/11/2018

Job Snapshot

Job Description

Join us on our exciting journey!

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
PURPOSE
Apply clinical research expertise to provide project related assistance across complex and multiple  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// trackers
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
Oversee and 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
Act as point of contact for assigned deliverables for specific customers or projects
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
Escalate quality issues to relevant stakeholders and/or line manager.

Job Requirements

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Advanced knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements;
     i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Familiarity with related systems and software utilized in clinical operations.  
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       
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Bachelor's degree in life sciences or related field and min 3 years with  relevant clinical research experience; or equivalent combination of education, training and experience
“Join Us”

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.

Whatever your career goals, we are here to ensure you get there!

We invite you to join IQVIA™.

Job ID: 1627076

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