- Competitive compensation + commission scheme
- Attractive benefits (security, flexibility, support and well-being)
- Engaging employee programs
- Technology for hybrid working and great onsite facilities
- Attend client meetings as appropriate to understand data collection requirements.
- Review standard CLARIO and non-standard data specifications and interact with the Data Manager (DM) to finalize specifications.
- Develop programs to create Clario standard and non-standard data files.
- Participate in the validation of encoding programs which generates CLARIO standard and non-standard data files.
- Performing ad-hoc programming activities utilizing raw data based on internal and external requests for:
- Get exposed to all modalities.
- Review User Requirements and create, review and approve Functional and Technical Specifications.
- Work with data management in providing programming support for DM activities including data review.
- Prepare and participate in internal and external audits.
- Represent the service line through the NPI (New Product Initiative) process.
- Identify opportunities to improve the methodology and provide practical solutions for problems.
- Contribute to the development of best practices to improve quality, efficiency and effectiveness.
- Drive client deliverables by performing the role of CDP SME when attending Project Management, Data Management or CDO meetings.
- Organize team resources to meet client needs.
- Lead and Mentor a team of Clinical Data Programmers:
- Develop the orientation and training plan for assigned Clinical Data Programing personnel.
- Oversee training of new Clinical Data Programmers.
- Assist with orientation and training of personnel as determined by management.
- Contribute to process development. Review and development of SOPs and associated documents related to Clinical Data Programming activities.
- Complete administrative tasks as needed within Clinical Data Programming.
- Mentoring other Clinical Data Programming resources.
- Participate in new hire interviews and provide feedback to management
- BS/BA Degree in Life Sciences or related field preferred or BS/BA Degree in computer sciences or related field
- SAS ADVANCED certified
- Ideally five or more years of experience in a pharmaceutical company or a CRO as a SAS Programmer – experience in SAS/BASE, SAS/MACRO and SAS/SQL products and procedures and one or more years of experience in database design and data structures
- Understanding of the pharmaceutical drug development process, as gained through a minimum of five years of experience in the pharmaceutical or healthcare industry.
- Strong organization, analytical and communication skills.
- Detail-oriented
- Extensive experience in implementing CDISC SDTM and Define standards including EG, CO, DM, RE, VS, SUPP CDISC SDTM domains.
- Experience with Windows and Microsoft Office products preferred.
- Strong written and verbal communication skills.
- Fluency in English (spoken and written).
- Experience with another programming languages is a plus.
- Proven experience working with large, complex real-world data sets (more specifically, patient data)
- Knowledge of technical and regulatory requirements related to the role.
- Excellent time management skills, contributing to multiple projects with competing timelines.
- Leadership/Mentoring skills: Proven ability to motivate people, instill accountability and achieve results.
- Prior leadership experience a plus.
-
Data Programmer
3 weeks ago
Labcorp Bengaluru, Karnataka, IndiaLead data management during start up. · - Act as a data liaison between Clinical Data Management and all other Covance departments and business units. · - Manage all client queries. · - Assist in identification and initiation of process improvement activities. · - Create standard ...
-
Clinical Data Programmer
2 weeks ago
Novo Nordisk Bengaluru, India**Department**:Data Systems & Automation, Bangalore Global Development · **About the department** · Data Systems & Automation, Bangalore Global Development GBS is one of the most competent and diverse team of professionals who are mainly responsible for providing functional and s ...
-
Clinical Data Programmer Ii
3 weeks ago
Novotech Asia Bengaluru, India**Brief Position Description** · The core responsibility for this position is as a member of the Data Management department at Novotech. The Clinical Data Programmer-II (CDP-II) will be responsible for programming activities on clinical trial projects and to ensure compliance wit ...
-
Data Facilitation Programmer
3 weeks ago
Novo Nordisk A/S Bengaluru, IndiaDepartment: Data Systems & Automation (DSA) · Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment? Are you best at what you do? If ...
-
Data Facilitation Programmer
3 weeks ago
Novo Nordisk A/S bangalore, IndiaData Facilitation Programmer · Department: Data Systems & Automation (DSA) · Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment ...
-
Data Facilitation Programmer
3 weeks ago
Novo Nordisk Bengaluru, IndiaDepartment: Data Systems & Automation (DSA) · Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment? Are you best at what you do? If ...
-
Assoc Data Programmer
3 weeks ago
IPL Labcorp Laboratories India Private Limited Bangalore, India Full timeEssential Job Duties: · Strong SQL knowledge · Informatica knowledge is a preference · Lead data management during start up. · Act as a data liaison between Clinical Data Management and all other Covance departments and business units. · Manage all client queries. · Provide ge ...
-
Clinical Data Programmer Iii Sas
3 weeks ago
Novotech Asia Bengaluru, IndiaNovotech is the Asia-Pacific CRO designed for biotech, accelerating clinical development via cutting-edge technology to improve patient lives. · Working in a fast-paced and adaptable environment, we strive to set the benchmark for both business and clinical trial performance acro ...
-
Clinical Data Programmer
2 weeks ago
ICON Strategic Solutions Bengaluru, IndiaDevelop solutions and recommendations for Medidata Rave custom forms, folder, and matrix structures, edit checks, derivations, custom function Edit Checks, and end user guides. Rave Study Build and Validation in support of in-house and outsourced trials globally, of various level ...
-
Programmer - Data Standards and Sdtm Delivery
3 weeks ago
GSK Bengaluru, Karnataka, India**Site Name**: Bengaluru Luxor North Tower · **Posted Date**: May · **Job qualification needed**: · 1. Minimum 3 years to 5 years of experience into SAS & SDTM must · 4. No WFH or other locations are provided. · - Assist in the development, validation, and review of study & stan ...
-
Clinical Data Programmer Iii Sas
3 weeks ago
Novotech Asia Bengaluru, India**About the** **role;** · **Responsibilities**: · 1.Projects/Clinical Studies · - Participate in Client and Project meetings as required in consultation with the Team Lead CDP to explain the CDP requirements, process and through-put times. · - Undertake database configuration, pr ...
-
Clinical Data Programmer
2 days ago
ICON Strategic Solutions Bengaluru, IndiaDesign and set-up of study database for data collection in clinical trials based on protocol needsSet up of models and performing transformation updates in DMWMapping of metadata and clinical data from source system(s) to DMW (Data Management Workbench)/ CDW (Clinical Data Wareho ...
-
Clinical Data Programmer
3 weeks ago
ICON Strategic Solutions Bengaluru, IndiaDevelop solutions and recommendations for Medidata Rave custom forms, folder, and matrix structures, edit checks, derivations, custom function Edit Checks, and end user guides. Rave Study Build and Validation in support of in-house and outsourced trials globally, of various level ...
-
Data Programmer
1 week ago
Labcorp Bengaluru, Karnataka, IndiaEssential Job Duties: Lead data management during start up. Act as a data liaison between Clinical Data Management and all other Covance departments and business units. Manage all client queries. Assist in identification and initiation of process improvement activities. Create st ...
-
Lead Clinical Data Programmer
2 days ago
Elanco Bengaluru, India Full timeAt Elanco (NYSE: ELAN) – it all starts with animals · As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. We're driven by our vision of 'Food and Companionship Enriching Li ...
-
Lead Clinical Data Programmer
2 weeks ago
Clario Bengaluru, IndiaAre you a seasoned Clinical Data Programming professional looking for an opportunity to join an industry leading data technology organisation in the clinical research space? Clario are looking for a Lead, Clinical Data Programmer to join our well established team in India, workin ...
-
Associate Lead Data Facilitation Programmer
3 weeks ago
Novo Nordisk Bengaluru, IndiaDepartment – Clinical Drug Development - Global Business Solutions · Are you passionate about quality and simplification? Do you want to build quality within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment and s ...
-
Programmer - Data Standards and SDTM Delivery
3 weeks ago
14260 GSK India Global Services Private Limited Bengaluru, India Full timeDescription · : · • Assist in the development, validation, and review of study & standard programs/macros (Including SAS, CQL, PL/SQL, SPOTFIRE, R-Programming, Python) that support standard and study-level conversion of clinical trial data. · • Be able to develop and validate ...
-
Data Facilitation Programmer
3 weeks ago
Novo Nordisk A/S Bengaluru, IndiaDepartment: · Data Systems & Automation (DSA)Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment? Are you best at what you do? If s ...
-
Data Facilitation Programmer
1 week ago
Novo Nordisk Bengaluru, Karnataka, IndiaData Facilitation Programmer · **Category**:Data & AI**Location**:Bangalore, Karnataka, IN- Data Facilitation Programmer**Department**:Data Systems & Automation (DSA)- · **About the department** · - Data Systems & Automation (DSA), Data Management, Bengaluru is one of the most co ...
Lead Clinical Data Programmer - Bengaluru, India - Clario
![Default job background](https://contents.bebee.com/public/img/bg-user-ex-1.jpg)
Description
Are you a seasoned Clinical Data Programming professional looking for an opportunity to join an industry leading data technology organisation in the clinical research space? Clario are looking for a Lead, Clinical Data Programmer to join our well established team in India, working alongside a global team of data specialists to provides our customers with best in class data to support the development of life changing therapies from clinical trials.
What we offer
What you will be doing
Lead and Mentor a team of Clinical Data Programmers, Create and test SAS code used for standard and non-standard data file creation; Review Clario standard and non-standard data specifications.
a. Esoteric quality control checks requested by QC.
b. Data resolution/Mining.
c. Other client requirements.
What we look for
At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives. We value the contribution each of our people brings. It's only through our people that we can continue to innovate technology that will shape the future of clinical trials.
EEO Statement
Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.