Clinical sas programmer Jobs

Clinical Data Management Programmer II
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- Microsoft Powerpoint
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- Health insurance
- Paid time off
Quick apply
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- Email
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Senior Programmer Submission
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- Full-time
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サイネオス・ヘルス —Pune, Maharashtra
- Microsoft Powerpoint
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Navitas Life Sciences —Chennai, Tamil Nadu
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Medtek.AI —Nagar, Uttar Pradesh
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ICON Plc —Chennai, Tamil Nadu
- Full-time
- Microsoft Word
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- Microsoft Outlook
- Health insurance
Principal Statistical Programmer
Kenvue —Bengaluru, Karnataka
- Hybrid work
- Computer Science
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Clinical Data Management Programmer II

Quanticate -
Bengaluru, Karnataka

Quick apply

Job details

Contractual / Temporary

Benefits

Health insurance
Paid time off
Flexible schedule
Paid sick time

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Visual Basic
SAS
C#
Microsoft Office
.NET
Master's degree
SQL
Bachelor's degree
Data management
Clinical trials
PL/SQL
Communication skills

Full job description

Join a dynamic and growing clinical research organisation at the forefront of data-driven innovation in clinical trials. We are committed to delivering high-quality, reliable data solutions that accelerate drug development and improve patient outcomes worldwide. Our collaborative, fast-paced environment empowers talented professionals to make a meaningful impact while continuously developing their skills.

This is an exciting opportunity for a detail-oriented and technically strong CDM professional to expand their expertise, contribute to process improvements, and work with industry-leading tools in a highly collaborative environment.

What You’ll Do

Work as a Clinical Data Management (CDM) Programmer supporting clinical studies.
Perform technical and programming tasks for assigned projects, ensuring high data quality and compliance.
Design and implement complex edit checks, data validations, and derivations.
Set up, manage, and validate electronic data imports and exports.
Prepare datasets and documentation for study completion and regulatory submissions.
Conduct quality control (QC) checks on programming outputs.
Support reporting programming and ensure timely delivery against project schedules.
Monitor systems for workflow alerts, performance issues, and resolve programming defects.
Contribute to process improvements, standardisation, and best practices.
Manage User Access Management (UAM) for EDC studies and maintain related documentation.
Collaborate with cross-functional teams and support system integrations, updates, and UAT activities.
Ensure compliance with study standards, SOPs, and regulatory requirements.

What You’ll Gain

Hands-on experience with leading EDC platforms and advanced clinical programming tools.
Exposure to global clinical trials and collaboration with sponsors and cross-functional teams.
Opportunities to contribute to process improvements and innovation initiatives.
Continuous learning through training, literature, and professional development programs.
Experience in a dynamic, matrix-structured work environment.

Quanticate is the world leading data-focused CRO, and we often work with our customers on their complicated clinical trials which require a high level of statistical programming, statistics and data management input. We need talented individuals to help us fulfil our customers’ needs.

Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical program, to small biotechs that are taking their first steps in clinical development

We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want – developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.

Requirements

Knowledge

Bachelor’s degree required; Master’s degree preferred.
Equivalent combination of education and relevant experience will be considered.
Understanding of clinical data management processes and standards.

Work Experience

Minimum 3+ years of experience in Clinical Data Management.
Experience supporting clinical trials and working with EDC systems.

Skills

Proficiency in EDC platforms such as Medidata Rave, Veeva, Medrio, Viedoc, etc.
Strong knowledge of SAS and clinical programming concepts.
Experience with programming languages such as PL/SQL, SAS, C#, or VB (preferred).
Familiarity with edit checks, derivations, database setup, and data validation processes.
Experience with application programming and system integrations.
Strong understanding of quality standards and SOP-driven environments.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
Excellent written and verbal communication skills.
Ability to collaborate with internal teams and external stakeholders effectively.
Experience in a matrix organisational structure is an advantage.

Quanticate will never ask for payments as part of the recruitment or hiring process, and all legitimate correspondence from Quanticate will come exclusively from our @quanticate.com domain name. Hiring at Quanticate is based purely on merit and we do not ask or require candidates to deposit any money or complete any paid for courses as part of the process. Further guidance on our recruitment process and tips on how to stay safe during your job search can be found on our website at https://www.quanticate.com/careers-guidance.

Benefits

Competitive salary
Flexible working hours
Holidays (Annual Leave, Sick Leave, Casual Leave and Bank holidays)
Medical Insurance for self and immediate family
Gratuity
Accidental Coverage
Quanticate offers a variety of different learning development opportunities to help you progress (mentoring, coaching, e- learning, job shadowing)

Quick apply

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