Iqvia Clinical SAS Programmer Recruitment
- IQVIA Clinical SAS Programmer Job Vacancies
- IQVIA Hiring Clinical SAS Programmer
- Job Overview
- Key Responsibilities
- Qualifications and Skills
- How to Apply
IQVIA Clinical SAS Programmer Job Vacancies
Are you ready to take your career to the next level with IQVIA, a global leader in healthcare and clinical research solutions? IQVIA is hiring Clinical SAS Programmers in Kochi, India, for exciting full-time positions. If you have expertise in clinical data programming and a passion for driving innovation in healthcare, this role is tailored for you.
IQVIA Hiring Clinical SAS Programmer
IQVIA combines advanced analytics, cutting-edge technology, and deep domain expertise to transform healthcare delivery worldwide. As a Clinical SAS Programmer, you’ll play a pivotal role in designing, managing, and maintaining clinical databases that are critical to the success of global clinical trials.
Job Overview
Position: Clinical SAS Programmer
Location: Kochi, India (with opportunities available in additional locations)
Job Type: Full-Time
Job Reference: R1452040
As a Clinical SAS Programmer, you will take charge of developing and managing clinical databases, ensuring data integrity, and providing technical expertise to internal and external stakeholders.
Key Responsibilities
As Database Management Specialist your primary responsibilities are:-
- Serve as Lead Programmer.
- Plan and coordinate database design, development, implementation, maintenance, and user support of clinical systems.
- Provide advanced technical expertise in conjunction with internal and external clients.
- Program, test, and document databases in accordance with programming standards and validation procedures.
- Program database manipulations and transfers of data for internal and external clients.
- Mentor other team members and Lead Programmers in training and developing technical and/or database expertise.
- Independently bring project solutions to the CDP teams and the Clinical Data Programming department.
- Collaborate with IT in evaluating and/or developing and implementing new technologies.
- Develop, revise, and maintain core operating procedures and working instructions with CDP management.
- Meet milestones as assigned, and interact with the project team to organize timelines, responsibilities and deliverables.
- Develop and maintain good communications and working relationships with teams and external clients.
- May interact with corporate team and CDM team members to negotiate timelines, responsibilities, and deliverables
- Ability/ potential on process innovations and/or improvements
Qualifications and Skills
To succeed in this role, candidates must meet the following requirements:
- Educational Background:
- Bachelor’s degree in Computer Science, Life Sciences, or a related field.
- Equivalent combinations of education, training, and experience are also considered.
- Experience:
- Minimum 3 years of relevant work experience in clinical data programming.
- Technical Skills:
- Advanced knowledge of SAS, Oracle, Python, and R.
- Familiarity with technologies like VGL, BizTalk, C#, and .NET is advantageous.
- Domain Knowledge:
- Solid understanding of the clinical drug development process.
- Soft Skills:
- Excellent organizational and communication abilities.
- Strong problem-solving and relationship-building skills.
How to Apply
Take the first step toward an impactful career by applying for the Clinical SAS Programmer position at IQVIA.
Click here to apply: IQVIA Job Application.
To apply for this job please visit jobs.iqvia.com.