Senior Clinical Data Management SAS Programmer

IQVIA; Bengaluru; On-site; INR 3,000,000 - 5,500,000; Full time

Job summary

IQVIA in Bengaluru seeks a Senior Clinical Data Management SAS Programmer Lead to oversee CDM activities and lead programming efforts for clinical databases. You will plan, design, implement, and maintain systems while providing advanced technical expertise to internal and external clients.

Responsibilities include programming, testing, documenting, mentoring, meeting milestones, and collaborating with IT. Strong clinical domain knowledge and communication are essential for success in this role.

Qualifications

• Bachelor's degree in computer science, life sciences or related field.
• 8+ years of relevant work experience required.
• Advanced knowledge of Oracle, SAS, Python and R; leading technologies a plus.
• Laboratory Data Programming: VGL, BizTalk, C#, .NET.

Responsibilities

• Lead Programmer for CDM projects and coordinate database design and maintenance.
• Program, test, and document databases per standards and validation procedures.
• Mentor team members and lead programmers in technical skills.
• Collaborate with IT to evaluate new technologies and implement improvements.
• Develop, revise, and maintain SOPs and working instructions.

Skills

SAS

Python

R

Oracle

Clinical Data Programming

Education

Bachelor's Degree in Computer Science or Life Sciences

Tools

BizTalk

C#

.NET

VGL

Job description

Clinical Data Management SAS Programmer Job Overview

• 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.

Qualification

• Bachelor's Degree Computer/life science or related field Req.
• Minimum 8 years of relevant work experience Required.
• Equivalent combination of education, training and experience Req.
• Clinical Data Programming: Advanced knowledge of Oracle, SAS, Python and R. Knowledge/ experience on leading technologies would be an added advantage.
• Laboratory Data Programming: Advanced knowledge of VGL and/or BizTalk and/or C# and/or .NET.
• Solid understanding of clinical drug development process (strong clinical domain knowledge).
• Excellent organizational, communication, and technical database skills.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.

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.

Experience Level Senior Level