Hi Associate,
|
Currently, I am recruiting candidates for one of my requirement as mentioned below. If you have a matching profile, please send me the updated resume along with contact details at the earliest.
|
| Job Title |
SAS Clinical Programmer |
| Project Location |
Woodcliff NJ |
| Duration |
12 months /Contract
|
Skills Required and Job Description:
Interview Mode:: F2F required after telephonic
Main purpose of the job:
- To support the Biostatistics team by carrying out and overseeing programming activities of statistical programmers and external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies.
- Must contribute to the overall efficiency and best practice running of the Biostatistics group, demonstrating the ability to work efficiently and to a high standard within a clinical team environment.
Main duties/responsibilities:
- Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following areas: analysis datasets, statistical tables, figures, listings, Integrated Summaries of Safety (ISS), Integrated Summaries of Efficacy (ISE), electronic submissions and other internal and external requests (e.g., publications). Accessing and converting data to SAS from Database management system and PC file formats (e.g., MS Excel, text files). Working with external vendors in order to develop or monitor the content and structure of SAS data sets.
- Developing and maintaining SOPs, SWPs and other related technical documents, providing input to the Database and CRF Development, creating edit check programs and providing feedback to the Data Management. Providing input in developing statistical analysis plans, specifications of analysis datasets, validation plans, and other related documents. Determining and researching SAS software upgrades and related systems and addressing maintenance issues.
- Managing and developing team, maintaining standards for programming activities, and guiding/coaching Statistical programmers.
- Working independently to accomplish tasks and goals defined by supervisor. Attending required training and meetings and bringing in new ideas to improve the programming process. Responsibilities weighting may change significantly based on the incumbent and their assigned areas of responsibility.
- Qualifications and education required: Minimum of Bachelor¿s degree in Statistics, Computer Science, Mathematics, or a related science discipline. Masters preferred.
Experience required:
- Minimum 5 years¿ experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. 7+ years¿ experience preferred.
- Some project experience in a pharmaceutical/CRO programming environment or demonstrated significant leadership of SAS programming activities in a clinical pharmaceutical/CRO environment.
- Skills and aptitude required:
- Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office.
- Proven experience with Unix and Windows operating systems.
- Must understand the software development life cycle, SDLC.
- Understanding of FDA guidelines.
- Good organization, time management and attention to detail skills needed to work in a stressful environment under tight deadlines while maintaining focus on details and quality.
- Applies good judgment and demonstrates initiative to resolve issues.
- Strong verbal, written and interpersonal communication skills needed to work effectively in a team environment, managing that team as required.
|
Regards,
Anchal Rastogi
(Deputy Resource Manager)
| RAMY Infotech Inc. |
| .........consulting redfined |
| Renaissance Business Center
1851, McCarthy Blvd, Suite#107
Milpitas, CA 95035 |
| Phone : 408-317-9256 x 335 |
| Fax : 408-273-6834 |
| Email : [email protected] |
| URL : www.ramyinfotech.com |
| Disclaimer: The information in this email is confidential and may be legally privileged. Access to this email by anyone other than the intended addressee is unauthorized. If you are not the intended recipient of this message, any review, disclosure, copying, distribution, retention, or any action taken or omitted to be taken in reliance on it is prohibited and may be unlawful. If you are not interested in receiving mails from us then please forward this mail with remove in the subject to [email protected] .Sorry for any inconvenience. E-mails sent from or to RAMY Infotech Inc. may be subject to our monitoring and recording procedures. |
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