IQVIA

TMF Document Specialist

In short

TMF Document Specialist role managing clinical trial records and document retrieval for IQVIA, a global clinical research and healthcare intelligence company, based in Dalian, China. The job covers filing accuracy, records center security, scanning processes, and may include team-lead duties on records management projects. It requires 3-4 years of experience in a clinical research environment, knowledge of ICH/GCP regulations and records management laws, strong organizational skills, and good English communication, along with physical tasks like lifting up to 18kg and possible shift work.

Essential Functions
•Perform assigned complex administrative tasks to support team members with project execution
•Assist in updating and maintaining complex data in systems within project timelines and per project plans
•Coordinate the retrieval of records requested by users and prepare closed studies to final destination within agreed timelines
•Conduct and manage scanning processes and train staff on scanning processes
•Interface with departments to support retrieval projects and ensure information needs are met
•Serve as primary contact for internal/external clients
•Monitor and review filing accuracy and compliance to IQVIA or customer file plans and Standard Operating Procedures (SOPs) where applicable
•Maintain records center security to protect record integrity by ensuring compliance to SOPs
•May coordinate transfer, recall, and disposition of records to commercial records storage centers
•Oversee disposal of obsolete records and ensure efficient maintenance of records storage space, supplies, and equipment
•Train team members on records management tasks, policies, and procedures
•Establish and maintain effective internal and external client communications
•Design and administer records management systems and processes
•Ensure project deadlines, commitments, and goals are met by monitoring projects daily outputs
•May function as team leader for records management projects
Qualifications
•High School Diploma or equivalent
•3-4 years' experience working in relevant clinical research environment. Equivalent combination of education, training and experience.
•Good knowledge of applicable clinical research regulatory requirements; i.e., International Conference on Harmonization (ICH), Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines
•Knowledge of technology applications relevant to records center environments
•General knowledge of computer technology and software programs, and accurate data entry skills
•Attention to detail and accuracy in work
•Ability to achieve productivity despite time pressure constraints
•Good problem solving skills
•Strong organizational, planning, and decision making skills
•Good time management and prioritization skills
•Extensive knowledge of records management laws and regulations
•Excellent oral and written communication skills including good command of English language
•Ability to manage and lead others
•Ability to establish and maintain effective working relationships with internal and external clients
•Position requires a significant amount of writing and keyboarding involving repetitive motions with fingers and sitting for prolonged periods of time
•Position is required to stand, walk, sit, use hands to manipulate, handle or feel, and reach with hands and arms
•Position is required to stoop, kneel and may need to utilize a ladder for paper files on high-density file systems
•Unaided lifting of objects up to 40 pounds/18kgs
•May require to work in shifts
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

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