Senior Records Management AssociateRecords Management Analyst 1
Pasig - Philippines
Job Summary
Job Overview
Provide Trial Master File (TMF) - Quality checks related assistance to study teams.Apply Clinical Research Records Management expertise to provide project related assistance across multiple project(s) sites and project teams.
Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs) policies practices good clinical practices applicable regulatory requirements and meets quality and timeline metrics.
May lead teams functionally where assigned including awareness of scope of work budget and resources.
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
Monitor filing accuracy and compliance to IQVIA or customer file plans and Standard Operating Procedures (SOPs);
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
Assist management with the implementation of strategic goals plans cost proposals and resource projections for records management projects.
May function as team leader for records management projects.
Qualifications
Bachelors Degree Records management or related field.
3-4 years experience working in a Records Management technically-related area. Equivalent combination of education training and experience.
Strong knowledge of applicable research and regulatory requirements Conference on Harmonization (ICH) Good Clinical Practice (GCP) and relevant local laws regulations and guidelines.
Knowledge of technology applications relevant to records management environments.
General knowledge of computer technology and software programs and accurate data entry skills.
Ability to perceive and analyze problems develop solutions and make sound decisions.
Ability to handle multiple tasks and projects within defined timelines and balance competing priorities.
Attention to detail and accuracy in work.
Ability to remain focused with regards to details under pressure.
Strong organizational planning and decision making skills.
Excellent oral and written communication skills including good command of English language.
Ability to establish and maintain effective working relationships with internal and external clients.
Ability to lead others.
Position requires a significant amount of writing and keyboarding involving repetitive motions with fingers and sitting for prolonged periods of time.
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.
Required Experience:
Senior IC
About Company
IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more