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Statistical Programmers

Job Field:
IT & Data Management Jobs
Discipline:
Statistics Programmer Jobs
Country:
India
Region:
India All
Contract Type:
Permanent
Currency:
Unspecified
Salary Description:
Competitive
Posted:
16-Jul-19
Recruiter:
Clintec
Job Ref:
3582

Are you a SAS Programmer interested in a new challenge with an award-winning, global CRO?
Clintec is a business built around people who strive for excellence, and we currently have an exciting opportunity available for an experienced Clinical Data Manager to join our team in the India supporting various client. The role will be Office based, so we can consider candidates working in Bangalore.

Role Purpose
A SAS Programmer will be expected to lead and/or support programming activities and produce associated documentation involved in reporting of clinical trials in accordance with the protocol, standard operating procedures (SOPs), good clinical practices (GCP) and other applicable regulatory requirements. They will be leading and/or support the specification, programming and documentation of SDTM and ADaM datasets and generation and validation of Tables, Listings and Figures for individual studies and study programmes.
As a technical expert, they will be expected to support relevant internal and external users for CDISC compliance and documentation. Where appropriate, mentoring and support of junior SAS programming staff, peers and other department staff is expected

Key Accountabilities
Responsible for leading and/or supporting SAS Programming across multiple clinical trials
Produce SDTM and ADaM datasets, tables, listings and figures
Generate and maintain required specification and documentation
Review data management planning documentation, such as data management plan, edit check specifications, data transfer agreements
Proactively provide process improvement feedback to Management and provide input in SOP updates/development
Participate in audits as required
Assist in business development activities as required
Assist in developing programming related timelines
Assists in addressing external application vendor issues, integrations, and implementations
Collaborate with clients (as and when required), peers, project teams and/or requestors to clarify and finalise specifications
Maintain and continue to gain a broad overall knowledge in the field of clinical programming and clinical data management

WHY JOIN CLINTEC?
At Clintec, we understand that our people are our biggest asset and we value the hard work and dedication of all our employees.
By joining the Clintec team you can expect:
A competitive salary and benefits package including private healthcare, dental and vision cover, life assurance and flexible benefits
25 days annual leave plus public holidays
Real career development opportunities and a life-long career with an innovative, forward-thinking clinical research company

​Click Apply Now to send your CV of email us directly on careers@clintec.com for more information!

THE COMPANY
Clintec (an IQVIA company), established for 22 years, is an award-winning, full-service global clinical research organisation with our HQ office based in Scotland, UK. We support key product development and manage clinical trials in over 50 countries worldwide, across all major therapeutic areas, with expertise in Oncology and Rare Disease studies. We differ from other players in the clinical research industry as we combine the agility and flexibility typical of smaller CROs with the global coverage and management associated with large CROs.

Find out more by visiting www.clintec.com


KEY WORDS:
Clinical Data Manager / Data Manager / RAVE / Medidata Rave / Data Management / Data Programming / CDMS / Clinical Data Management System / ED

Closing Date:
13/08/2019

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