Sas programmer Jobs

Senior Lead Clinical Data Science Programmer
ICON Plc —Bengaluru, Karnataka
- Full-time
- Health insurance
6d
Senior Batch Specialist
Alight —Noida, Uttar Pradesh
- Computer Science
- Master's degree
- SQL
- Health insurance
- Flexible schedule
Principal Biostatistician (VAX)
Sanofi —Hyderabad, Telangana
- Doctoral degree
- English
- Research
DMCP-0, Senior Specialist, Clinical Data programming
Merck KGaA —Bengaluru, Karnataka
- Computer Science
- SQL
- Python
9d
Senior Statistical Programmer (Clinical Pharmacology)
サイネオス・ヘルス —Pune, Maharashtra
- English
- Travel
- Communication skills
CDM Programmer-2 ( Veeva EDC and CDB )
Thermo Fisher Scientific —Bengaluru, Karnataka
- Full-time
- SQL
- Project management
- Bachelor's degree
Senior Associate - RWE Obesity Statistical Programming
Amgen —Hyderabad, Telangana
- Computer Science
- English
- Master's degree
I&F Decision Sci Practitioner Manager
Accenture —Bengaluru, Karnataka
- Full-time
- Project management
- Machine learning
- Human resources
Principal Consultant – BI /DI
AxionConnect —Mumbai, Maharashtra
- Windows
- SQL
Senior ISV Infrastructure Software Engineer
Tech Pinacle Innovation Pvt Ltd —Noida, Uttar Pradesh
- ₹6,19,850.79 - ₹24,32,985.14 a year
- Weekend availability
- Hybrid work
- Windows
- Linux
- AI
Quick apply
Pr. Statistical Programmer (Clinical Pharmacology)
サイネオス・ヘルス —Yerawada, Pune, Maharashtra
- English
- Travel
- Mentoring
Clinical Data Svs Sr Analyst
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Analysis skills
- Bachelor's degree
Clinical Data Svs Associate Manager
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Communication skills
PRINCIPAL PROGRAMMER
Medtek.AI —Nagar, Uttar Pradesh
- Computer science
- Master's degree
- Bachelor's degree
Principal Clinical Programmer (Veeva)
Syneos - Clinical and Corporate - Prod —Hyderabad, Telangana
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
4d
Senior Biostatistician, Global Quality, Regulatory, Clinical Affairs
Cepheid —Bengaluru, Karnataka
- Full-time
- Doctoral degree
- Master's degree
- Machine learning
- Paid time off
2d
Statistical Programmer
Sun Pharmaceutical Industries, Inc. —India
- Hybrid work
- Computer Science
- Analysis skills
- Bachelor's degree
Principal Statistical Programmer FSP
Cytel Inc —India
- Full-time
- Remote
- Master's degree
- Analysis skills
- Bachelor's degree
Business Analysts
Triumphant ITCS —India
- Computer Science
- Data analysis skills
- Master's degree
Senior/ Principal Statistical Programmer | Long Term Contract | Remote
Two95 International Inc. —India
- Remote
- SQL
- Python
Quick apply

I want to receive the latest job alerts for sas programmer

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

sas programmer jobs near

Senior Clinical Data Analyst jobs in Bengaluru, Karnataka

Senior Software Engineer jobs in Noida, Uttar Pradesh

Biostatistician jobs in Hyderabad, Telangana

Principal jobs in Mumbai, Maharashtra

Clinical Data Analyst jobs in Bengaluru, Karnataka

Data Scientist jobs in Bengaluru, Karnataka

Senior Accountants jobs in Coimbatore, Tamil Nadu

Hcl, Analyst jobs in Lucknow, Uttar Pradesh

Senior Clinical Data Analyst jobs in Hyderabad, Telangana

Data Entry jobs in Indiranagar, Bengaluru, Karnataka

Senior Citizen, Part Time jobs in Navi Mumbai, Maharashtra

Senior Programmer jobs in Viman Nagar, Pune, Maharashtra

Senior Programmer jobs in Coimbatore, Tamil Nadu

Psychiatrist, Senior Resident jobs in Uttar Pradesh

Senior Management jobs in Chandigarh, Chandigarh

Senior Resident, Ent jobs in Chennai, Tamil Nadu

Senior Programmer jobs in Maharashtra

Senior Programmer jobs in Hyderabad Jubilee Ho, Hyderabad, Telangana

Regulatory Affairs Specialist jobs in Tandalja, Vadodara, Gujarat

Regulatory Affairs Specialist jobs in Hathijan, Ahmedabad, Gujarat

Senior Lead Clinical Data Science Programmer

ICON Plc -
Bengaluru, Karnataka

Apply Now

Job details

Full-time
6 days ago

Benefits

Health insurance

Qualifications

XML
SAS
Data management
Data science

Full job description

Senior Lead Clinical Data Science Programmer

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Senior Lead Clinical Data Science Programmer at ICON, you will be instrumental in leading the development and implementation of advanced data science solutions for clinical trials.

What You Will Do:

You will manage day-to-day clinical data science activities, supporting your team to deliver quality outcomes.

Key responsibilities include:

Lead the development of Data Transfer Specifications (DTS) documents to align external data providers and research partners on the required structure for new data. This includes:
Authoring the DTS, responding to external data providers and internal stakeholder queries to ensure
data will be delivered in the correct format and structure.
Track DTS status with external data providers across different data types and programs and ensure data completion dates are met for study timelines and deliverables.
Ensuring data structure based on the type(s) of data being used is consistent and compliant with appropriate data templates.
Ensuring data structure is consistent across each data provider and comply with appropriate data templates.
Support data reconciliation and data structure inquiry resolution.
Liaise cross functionally to facilitate the creation of new test codes.
Participate in the Clinical Study Team as an extended team member.
Oversee and train in the use of the DTS and other supplemental documents.
Contribute to improvement initiatives as it relates to external data process.
Ensure study teams adhere to CDISC standards as it relates to external data.
Comply with all pertinent regulatory agency requirements (Understand clinical protocols and requirement for Biomarkers/Imaging/eCOA data, blinding and analysis expectations).
Process change requests to update existing DTS.
Improve templates for existing DTS to ensure data harmonization and downstream analytics.
Provide external data management oversight to vendors, providing a pathway for functional discussions, partnership level processes & standards, portfolio status, communication, and escalation.
Review and contribute to eCRF and EDC builds as it relates to external data requirements.

Your Profile:

You will have solid clinical data science experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

Expertise in biomarker data types and/or Imaging data for oncology and non-oncology studies is preferred
Experience working with multiple data types/formats
Experience in managing clinical, biomarker data, eCOA and imaging data
Demonstrates broad knowledge of all applicable regulations including 21 CFR
Part 11, ICH-GCP Guidelines and CDISC standards for data collections.
Demonstrates advanced knowledge of Data Management processes and industry best practices.
Advanced knowledge and experience with extracting data into SAS, CSV, and
XML formats is required.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Apply Now

Refine Your Search

Senior Lead Clinical Data Science Programmer

Senior Batch Specialist

Principal Biostatistician (VAX)

DMCP-0, Senior Specialist, Clinical Data programming

Senior Statistical Programmer (Clinical Pharmacology)

CDM Programmer-2 ( Veeva EDC and CDB )

Senior Associate - RWE Obesity Statistical Programming

I&F Decision Sci Practitioner Manager

Principal Consultant – BI /DI

Senior ISV Infrastructure Software Engineer

Pr. Statistical Programmer (Clinical Pharmacology)

Clinical Data Svs Sr Analyst

Clinical Data Svs Associate Manager

PRINCIPAL PROGRAMMER

Principal Clinical Programmer (Veeva)

Senior Biostatistician, Global Quality, Regulatory, Clinical Affairs

Statistical Programmer

Principal Statistical Programmer FSP

Business Analysts

Senior/ Principal Statistical Programmer | Long Term Contract | Remote

I want to receive the latest job alerts for sas programmer

Related Searches

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected