Clinical Coding Analyst - Remote

QPL IQVIA RDS Poland Sp. z o.o.

México

Remote

MXN 1,128,000 - 1,693,000

Full time

8 days ago

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

IQVIA is seeking a Clinical Data Management professional based in Mexico for remote, full-time work. You will manage single and multi-service projects, ensure on-time quality deliverables, and provide expert coding with MedDRA/WHODD according to dictionaries and SOPs.

The role requires 3–4 years in clinical trials, strong English, and ability to work with global clients. Strong collaboration with CDM teams and client stakeholders is essential.

Qualifications

  • High School Diploma or equivalent in Pharmacy, Dental, Medical, Nursing, life sciences or related field.
  • Advanced English both written and communication skills, works in a global team.
  • 3/4 years of relevant experience in clinical trials within a similar function.
  • Excellent knowledge of Medical Dictionaries used for coding (e.g. MedDRA, WHODD, ICD9).
  • Thesaurus management experience and knowledge of Medical Terminology, Pharmacology, Anatomy, Physiology.

Responsibilities

  • Serve as internal or external point of contact on standalone coding studies or accounts.
  • Maintain post-coding dictionary up-versioning synonym and coding reconciliation to align coding to latest dictionary versions.
  • Perform Dictionary up-versioning activities.
  • Perform external verbatim coding of data from non-EDC sources in line with required coding dictionary versions.
  • Perform comprehensive quality control procedures.
  • Perform Serious Adverse Event (SAE) coding reconciliation activities.
  • Collaborate with customers and develop solutions and action plans for issues, escalations and road blocks.
  • Proactively identify, solve quality issues and deliver projects as per agreed timeline.
  • Identify and implement processes and quality improvement initiatives in the DM and coding function.
  • Provide review and expert opinion in developing, revising, and maintaining standard core operating procedures and work instructions.
  • Develop and maintain good communications and working relationships with the CDM team and client stakeholders.

Skills

Advanced English
Project management
Quality control

Education

High School Diploma or equivalent in life sciences or related field

Tools

MedDRA
WHODD
ICD-9
Medidata Rave

Job description

Job Overview

Manage single and multi-service projects, ensuring quality deliverables on time, within budget and to the customer’s satisfaction; Provide expert skills as part of a Clinical Data Management (CDM) team to provide quality data that meet customer needs.

Essential Functions
  • Serve as internal or external point of contact on standalone coding studies or accounts.
  • Maintain post-coding dictionary up-versioning synonym and coding reconciliation to align coding to latest dictionary versions.
  • Perform Dictionary up-versioning activities.
  • Perform external verbatim coding of data from non-EDC sources in line with required coding dictionary versions.
  • Perform comprehensive quality control procedures
  • Perform Serious Adverse Event (SAE) coding reconciliation activities
  • Collaborate with customers and develop solutions and action plans for issues, escalations and road blocks.
  • Proactively identify, solve quality issues and deliver projects as per agreed timeline.
  • Identify and implement processes and quality improvement initiatives in the DM and coding function.
  • Provide review and expert opinion in developing, revising, and maintaining standard core operating procedures and work instructions.
  • Develop and maintain good communications and working relationships with the CDM team and client stakeholders.
Qualifications and experience
  • High School Diploma or equivalent Pharmacy, Dental, Medical, Nursing, life sciences or related field qualification or educational equivalent.
  • Advanced English both written and communication skills, works in a global team.
  • 3/4 years of relevant experience in clinical trials within a similar function, including proven competence in managing the delivery of coding or/and other data management processes for multiple global projects, also including experience in handling complex customer negotiations and bid defense meeting.
  • Excellent knowledge of Medical Dictionaries used for coding (e.g. MedDRA, WHODD, ICD9, etc.).
  • Thesaurus management experience.
  • Excellent knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology required for many tasks.
  • Advanced knowledge of data management processes and systems and advanced ability to apply this knowledge in practice - Medidata Rave is preferred.
  • Excellent understanding of clinical drug development process (detail oriented).
  • Good project management skills related to all phases of clinical studies.
  • Excellent knowledge of operating procedures and work instructions and the ability to apply them in practice.
  • Based in Mexico, full time remote position.

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 https://jobs.iqvia.com 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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Clinical Coding Analyst - Remote
Clinical Coding Analyst - Remote

Iqvia • Mexico

Remote
MXN 420,000 - 620,000
Remote Clinical Coding Analyst — MedDRA/SAE Focus
Remote Clinical Coding Analyst — MedDRA/SAE Focus

IQVIA • Mexico

Remote
MXN 420,000 - 620,000
Remote Clinical Coding Analyst - MedDRA/SAE QC
Remote Clinical Coding Analyst - MedDRA/SAE QC

IQVIA Inc • Mexico

Remote
MXN 1,128,000 - 1,693,000
(Senior) Data Team Lead
(Senior) Data Team Lead

IQVIA • Ciudad de México

On-site
MXN 900,000 - 1,200,000
Clinical Trial Assistant
Clinical Trial Assistant

MSC Quintiles Mexico S. de R.L. de C.V. • Ciudad de México

Hybrid
MXN 180,000 - 300,000
null
Senior Statistical Programmer in Pharmacometrics (PM) support (Clinical Trials)
Senior Statistical Programmer in Pharmacometrics (PM) support (Clinical Trials)

IQVIA • Ciudad de México

Remote
MXN 1,719,000 - 2,533,000
Sr Database Management Specialist
Sr Database Management Specialist

MSC Quintiles Mexico S. de R.L. de C.V. • Mexico

Remote
MXN 900,000 - 1,500,000
Senior Clinical Programmer (Python)
Senior Clinical Programmer (Python)

IQVIA • Ciudad de México

Remote
MXN 600,000 - 1,200,000
Clinical Trial Manager II, IQVIA Biotech
Clinical Trial Manager II, IQVIA Biotech

IQVIA Inc • Ciudad de México

On-site
MXN 900,000 - 1,200,000
Principal Statistical Programmer (Clinical Trials)
Principal Statistical Programmer (Clinical Trials)

IQVIA • Ciudad de México

Remote
MXN 900,000 - 1,500,000