Ref #: 28757

Employment type: Permanent - Full-Time

Location: Chennai, Bangalore and Homebased

Posted: 22-May-2021

Description

If you are seeking a career where you can truly make a difference in the lives of others, working closely together with the top minds in the pharmaceutical Industry, then here is your chance. We are hiring a Clinical Research Associate II to work closely with our client, a leading pharmaceutical company.

Overview:

Responsible for mapping, programming, and validation of standardized clinical trial data and submission-ready tabulation packages.

Required experience and qualifications:
Job Title : Statistical Programmer - Senior/Principal (SDTM)
Job location : Chennai /Bangalore
Home based /Office based
No of years of experience: 5+ years of relevant exp in SDTM domain and SAS Skills
Education Qualification: Any graduation
Salary : As per Industry standards with attractive benefits
Skill set : Strong knowledge of SAS programming language, Define.xml, SDTM aCRF, cSDRGs

Key responsibilities :

• In-depth knowledge of protocol, current clinical drug development processes.
• Working knowledge of eDC systems - Rave is desirable.
• Expert knowledge of SAS programming language, Define.xml, SDTM aCRF, cSDRGs.
• Expert knowledge of data structures (e.g., CDISC SDTM, ADaM) and their implementation.
• Ability to work with cross-functional team interpreting data requirements.
• Strong project management skills are required.
• Prior experience of leading a programming team to manage timelines, resources and overall quality in a client-facing capacity is desirable.
• Demonstrated ability to perform assigned tasks independently and as part of a team.
• Demonstrated ability to successfully manage complex assignments, including competing tasks and timelines.
• Ability to liaise successfully with team members, management and externally with vendors and sponsors, as required.
• Advanced problem solving and organizational skills, attention to detail, etc.
• Good understanding of global clinical trial practices, procedures, methodologies and regulatory requirements (e.g., GCP, ICH).


Why join the DOCS team at ICON?

Working at ICON is more than a job, it’s a calling for people who care and are passionate about improving patients’ lives. At ICON, we care about our people and your passion, you are key to our success. We aim to provide an open and friendly work environment where we empower our people and provide them with opportunities to develop their long-term career.

At ICON you will have the opportunity to work with one of the global top 20 pharmaceutical companies, working on novel therapies that deliver real impact. If you want a career with a difference, ICON is the place for you.

#SAS #SDTM #Clinicalsasprogrammer #StatisticalProgrammer