Clinical Data Coder 1

Job Description

As a Clinical Data Coder at IQVIA, you will be responsible for providing quality data management products to the Data Management (DM) team to meet sponsor and company needs. Your role will involve performing Clinical Data Management and/or Coding activities, and you may also provide leadership in the role of the Lead Coder or in specific CDM tasks such as Data Operations Coordinator (DOC) or leading a coding related task on a mega trial.Key Responsibilities:- Serve independently as a Clinical Data Coder and/or Lead Coder or DOC for one or more protocols.- Manage delivery of coding activities and/or stand-alone coding projects through the full study life-cycle with minimal guidance.- Validate/test the coding application and programming of coding reports, and may also test coding related datasets, coding related edits, or any coding related programming activities.- Perform comprehensive data management and coding related tasks including conducting data review, writing and resolving data clarifications.- Manage coding related project timelines with guidance from the DOC or Data Team Lead (DTL) or Manager.- Perform Serious Adverse Event (SAE) reconciliation activities and may serve as a back-up for a Lead Coder, DOC, or DTL.- Perform comprehensive quality control procedures and assist in implementing new technology.- Independently bring coding and project related solutions to the DM team.- Handle audit requirements for respective studies including stand-alone coding projects as applicable.- Understand and comply with core operating procedures and work instructions.- Develop and maintain good communication and working relationships with the team.Qualifications:- Pharmacy, dental, medical, nursing, life sciences, or related field qualification or educational equivalent.- 2 years of relevant experience or equivalent combination of education, training, and experience.- Excellent knowledge of medical terminologies, pharmacology, anatomy and physiology.- In-depth knowledge of medical dictionaries used for coding (e.g., MedDRA, WHODD etc.).- Understanding of the Data Management process from study start-up through to database lock.- Ability to exercise excellent attention to detail and act independently with the initiative required to resolve problems.- Good understanding of database technologies related to data management and coding.- Knowledge of operating procedures and work instructions and the ability to apply them in practice.- Excellent written and oral communication skills in English language, organizational and leadership skills.- Ability to establish and maintain effective working relationships with co-workers, managers, and clients.- LPN - Licensed Practical Nurse - State Licensure RequiredIQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. They 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 Careers](https://jobs.iqvia.com). As a Clinical Data Coder at IQVIA, you will be responsible for providing quality data management products to the Data Management (DM) team to meet sponsor and company needs. Your role will involve performing Clinical Data Management and/or Coding activities, and you may also provide leadership in the role of the Lead Coder or in specific CDM tasks such as Data Operations Coordinator (DOC) or leading a coding related task on a mega trial.Key Responsibilities:- Serve independently as a Clinical Data Coder and/or Lead Coder or DOC for one or more protocols.- Manage delivery of coding activities and/or stand-alone coding projects through the full study life-cycle with minimal guidance.- Validate/test the coding application and programming of coding reports, and may also test coding related datasets, coding related edits, or any coding related programming activities.- Perform comprehensive data management and coding related tasks including conducting data review, writing and resolving data clarifications.- Manage coding related project timelines with guidance from the DOC or Data Team Lead (DTL) or Manager.- Perform Serious Adverse Event (SAE) reconciliation activities and may serve as a back-up for a Lead Coder, DOC, or DTL.- Perform comprehensive quality control procedures and assist in implementing new technology.- Independently bring coding and project related solutions to the DM team.- Handle audit requirements for respective studies including stand-alone coding projects as applicable.- Understand and comply with core operating procedures and work instructions.- Develop and maintain good communication and working relationships with the team.Qualifications:- Pharmacy, dental, medical, nursing, life sciences, or related field qualification or educational equivalent.- 2 years of relev

Keyskills :
Clinical Data ManagementCodingQuality ControlPharmacologyAnatomyPhysiologyCommunication SkillsLeadership SkillsData OperationsData ReviewMedical TerminologiesMedical DictionariesDatabase Technologies