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Clinical Job at IQVIA India – Clinical Data Coder Opportunity in Multiple Locations

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Explore this clinical job at IQVIA India for Clinical Data Coder roles. Apply now for iqvia careers, bds jobs, and medical jobs in Kochi, Kolkata, Bangalore, and Thane.
Clinical Job at IQVIA India | Clinical Data Coder

Clinical Job at IQVIA India | Apply now for a Clinical Data Coder Role

Looking for a rewarding clinical job in India’s leading healthcare analytics organization? IQVIA is hiring experienced professionals for the role of Clinical Data Coder (MedDRA, WHODD). This opportunity is ideal for candidates with 3+ years of experience in clinical data coding who want to grow their careers in clinical research, data management, and medical jobs across Kochi, Kolkata, Bangalore, and Thane.

Job Details:

  • Job Position: Clinical Data Coder
  • Experience: 3+ years of relevant experience in clinical data coding
  • Location: Kochi / Kolkata / Bangalore / Thane

About the Company:

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services for the life sciences industry. The company helps healthcare organizations accelerate innovation and improve patient outcomes through data-driven insights. IQVIA careers offer excellent growth, exposure to global trials, and opportunities in diverse medical jobs.

Job Description:

Provide comprehensive data management expertise (defined as efficient and quality data management products) to the Data Management (DM) team to meet sponsor and company needs. Perform Clinical Data Management and/or Coding activities, and may provide leadership either in the role of the Lead Coder or in a specific CDM task (e.g. Data Operations Coordinator (DOC) or lead a coding related task on a mega trial). This clinical job requires independent handling of coding responsibilities and contributing to overall data quality throughout the study lifecycle.

Qualifications:

  • Dental, medical, or related field qualification or educational equivalent.
  • 3 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 the 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 Req.

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 standalone coding projects through the full study life-cycle (with minimal guidance).
  • Validates/tests the coding application and programming of coding reports.
  • 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 and 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.
  • May serve as a backup 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.
  • Perform other duties as directed by the study team or Manager, or meet objectives as assigned.
  • Develop and maintain good communication and working relationships with the team.

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