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IQVIA

Runs drug trials and sells health data to pharma

TMF Specialist

Office Clerical & RecordsConfirmed live in the last 24 hours
Full-timeDalian, Liaoning, ChinaNo salary listedIn-person

About the Job

Requirements

  • A high school diploma or equivalent is required.
  • Three to four years of experience working in a relevant clinical research environment, or an equivalent combination of education, training, and experience, is required.
  • Knowledge of applicable clinical research regulatory requirements, including International Conference on Harmonization, Good Clinical Practice, and relevant local laws, regulations, and guidelines, is required.
  • Knowledge of technology applications relevant to records center environments is required.
  • General knowledge of computer technology and software programs, along with accurate data entry skills, is required.
  • Extensive knowledge of records management laws and regulations is required.
  • Oral and written communication skills, including a good command of English, are required.
  • The ability to manage and lead others and establish and maintain effective working relationships with internal and external clients is required.
  • The position requires writing and keyboarding involving repetitive finger motions and prolonged sitting.
  • The position requires standing, walking, sitting, using hands to manipulate, handle, or feel, reaching with hands and arms, stooping, kneeling, and potentially using a ladder for paper files on high-density file systems.
  • The position requires unaided lifting of objects up to 40 pounds (18 kilograms).
  • The position may require shift work.

Responsibilities

  • 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 according to project plans.
  • Coordinate retrieval of records requested by users and prepare closed studies for their 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 the primary contact for internal and external clients.
  • Monitor and review filing accuracy and compliance with IQVIA or customer file plans and applicable Standard Operating Procedures.
  • Maintain records center security to protect record integrity by ensuring compliance with Standard Operating Procedures.
  • Coordinate the transfer, recall, and disposition of records to commercial records storage centers, as needed.
  • 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 daily project outputs.
  • Function as team leader for records management projects, as needed.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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