Are you ready to take your career in clinical data programming to the next level? IQVIA, a global leader in clinical research services and healthcare intelligence, is offering an exciting opportunity for a Rave Programmer in Kochi and Bangalore, India. With a focus on innovation and improving patient outcomes, IQVIA is the perfect place to grow your expertise and contribute to cutting-edge clinical research.
About IQVIA
IQVIA is a premier provider of advanced analytics, technology solutions, and contract research services to the life sciences industry. We are committed to accelerating the development and commercialization of innovative medical treatments, helping healthcare organizations worldwide improve patient outcomes and overall health. At IQVIA, you’ll find an environment of collaboration, innovation, and growth.
Responsibilities in the Role
As a Rave Programmer, you will play a pivotal role in clinical data management, ensuring the seamless execution of clinical trials through efficient database design and development. Your responsibilities will include:
- Database Management
- Planning and coordinating database design, development, implementation, and maintenance.
- Supporting user requirements for clinical systems.
- Module Development
- Building and maintaining new modules and global libraries for clinical trials.
- Collaborating with Data Management to modify existing modules.
- Data Standards Implementation
- Applying clinical data standards and data models in database and global library development.
- Resolving delivery issues and escalating concerns to leadership when necessary.
- Library Maintenance
- Documenting and maintaining global library objects for study-level databases.
- Coordinating with study teams to ensure efficient database creation and modifications.
- Technical Expertise
- Developing metadata specifications for clinical data collection, transformation, and submission.
- Testing and maintaining CDMS validations and derivation procedures using SQL, PL/SQL, C#, VB script, or SAS.
Required Qualifications
To succeed in this role, candidates should meet the following requirements:
- Educational Background
- Bachelor’s degree in Computer Science, Life Sciences, or a related field, or equivalent education and experience.
- Experience
- Minimum 2 years of experience in clinical database programming, clinical database setup, and CRF design.
- Technical Skills
- Proficiency in RAVE programming, including global library maintenance and custom function programming.
- Basic understanding of CDISC standards and clinical data management systems.
- Experience with scripting languages and relational databases.
- Soft Skills
- Strong attention to detail, time management, and customer focus.
- Ability to effectively communicate technical concepts to non-technical users.
Desired Skills
- Development of validation and derivation procedures.
- Knowledge of clinical trial processes and metadata implementation.
- Familiarity with Global Library Conventions for data modeling and CDMS implementation.
