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Junior Clinical Data Programmer, Pharmiweb

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Reading

Hybrid

GBP 30,000 - 50,000

Full time

5 days ago
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Job summary

An innovative company is seeking a Junior Clinical Data Programmer to join their dynamic team. This hybrid role allows you to leverage your technical expertise in clinical studies, focusing on data integration. You'll be responsible for programming data exports, managing clinical study activities, and creating listings in various formats. Ideal candidates will have a Master's degree in a related field and proficiency in SAS and SQL. This is a fantastic opportunity to contribute to impactful projects in the life sciences sector, working in a collaborative environment that values your skills and growth.

Qualifications

  • 2 years of experience in programming/data management in a biometric department.
  • Proficiency in safety integration with E2B format and data lakes.

Responsibilities

  • Programming data exports from various sources for clinical studies.
  • Managing activities and creating listings in multiple output formats.

Skills

SAS
SQL
Python
Snowflake
Spotfire
InForm
Medidata Rave

Education

Master's degree in science/computer science

Tools

Databases

Job description

Junior Clinical Data Programmer
Flexible location: Reading UK or Strasbourg, France
Hybrid role
Job Overview:

Join our dynamic team as a Clinical Data Programmer and utilize your technical expertise in the exciting field of clinical studies. In this pivotal role, you will have the opportunity to plan and coordinate the implementation of clinical studies, with a special emphasis on data integration.

Responsibilities:

Your day-to-day tasks will involve:

  1. Programming data exports from various sources
  2. Managing activities on clinical studies
  3. Creating listings in multiple output formats

You will have the chance to work primarily with SAS and also using databases. We are particularly interested in professionals proficient in languages such as SAS and SQL. Additional skills in Python, Snowflake, Spotfire, or knowledge of clinical systems like InForm and Medidata Rave are a plus.

Qualifications:
  1. Master's degree or equivalent in science/computer science or related field
  2. 2 years of work experience in programming/data management within a biometric department
  3. Knowledge of InForm and Rave EDC
  4. Proficiency in safety integration with E2B format
  5. Understanding of data integration and data lakes
  6. Excellent organizational, communication, and technical database skills
  7. Ability to establish and maintain effective work relationships

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.

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