Clinical DM SAS Programmer (Kochi)

Iqvia; Ernakulam; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

IQVIA in India is seeking a Database Management Specialist responsible for leading programming efforts, planning and coordinating database design, development, and maintenance for clinical systems. You will mentor team members and work with clients to deliver validated data solutions.

The role requires a Bachelor's degree in Computer Science or Life Sciences, 5+ years of experience, and advanced knowledge of Oracle, SAS, Python and R.

Qualifications

• Bachelor's degree in Computer or Life Science, or related field.
• Minimum 5 years of relevant work experience.
• Advanced knowledge of Oracle, SAS, Python and R; leading technologies a plus.
• Laboratory Data Programming: VGL and/or BizTalk and/or C# and/or .NET.

Responsibilities

• Lead programming efforts and mentor team members.
• Plan and coordinate database design, development, implementation, maintenance and user support of clinical systems.
• Provide advanced technical expertise with internal and external clients.
• Program, test, and document databases per standards and validation procedures.
• Collaborate with IT to evaluate and implement new technologies.
• Develop and maintain core operating procedures and work instructions.

Skills

Lead Programmer

Database design

SAS

Python

R

Oracle

Communication

Education

Bachelor's Degree in Computer Science/Life Science

Tools

Oracle

SAS

Python

R

BizTalk

C#

.NET

VGL

Job description

Job Overview

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

• - Bachelor's Degree Computer/life science or related field Req - Minimum 5 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

Company Overview

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 creative 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.

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