Clinical DM SAS Programmer

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

Qualification

Bachelors 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/

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

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.