Excellent Career Opportunity With TCS Noida For Statistical Programmer JobsCafe.com Job Description - In-depth knowledge in Statistical Concepts(e.g. Design of Experiment, Linear model, Inferential Statistics etc.), Knowledge in Statistical software like SPSS/SAS (Base SAS, SAS/STAT), Good in communication skill.( Clinical Trials Space)
Post your Resume in Shine for more Matching Jobs - Click here to Register Today!Desired Profile Position Title - Statistical Programmer
Immediate Supervisor - Project Leader
Minimum Qualifications- M. Sc. (Stats/Mathematics/Operation Research-OR)
Required for the Role- In-depth knowledge in Statistical Concepts(e.g. Design of Experiment, Linear model, Inferential Statistics etc.), Knowledge in Statistical software like SPSS/SAS (Base SAS, SAS/STAT), Good in communication skill.
Responsibilities:
-Understand study documents (Protocol, CRF, SAP)
-Develop data analysis plans in collaboration with Statistical colleagues, physicians and other clinical staff. Establish a reporting database and analyze clinical trial data using SAS.
-Create Safety and Efficacy Table Figure Listing (TFL).
-Generate macros, listings and tables as part of Statistical analysis in the clinical Trials Space.
-Attend Project teleconferences with the customer.
-Adherence to industry standards and regulatory requirements, including but not exclusive to Good clinical Practices (GCP) and ICH guideline on Statistical Principles for clinical Trials.
-Participate in task forces/initiatives.
-Enhance technical skills relevant to statistics and programming.
EXP - 2 to 6 Years
Position Title – Sr. Statistical Programmer
Immediate Supervisor - Project Leader
Minimum Qualifications - Ph. D or M. Sc. (Stats/Mathematics/Operation Research-OR)
Required for the Role - In-depth knowledge in Statistical Concepts (e.g. Design of Experiment, Linear/Non-Linear model, Inferential Statistics, Survival Analysis etc.), Knowledge in Statistical software like SPSS/SAS (Base SAS, SAS/STAT, SAS Macro), Good in communication skill, Good understanding of Clinical Trial and its Phases (preferred).
Responsibilities:
-Understand study documents (Protocol, CRF, SAP)
-Develop/Review data analysis plans in collaboration with Statistical colleagues, physicians and other clinical staff. Establish a reporting database and analyze clinical trial data using SAS.
-Create/Review Safety and Efficacy TFL.
-Perform QC checks for TFL.
-Generate macros, listings and tables as part of Statistical analysis in the clinical Trials Space.
-Attend Project teleconferences with the customer.
-Adherence to industry standards and regulatory requirements, including but not exclusive to Good clinical Practices (GCP) and ICH guideline on Statistical Principles for clinical Trials.
-Participate in task forces/initiatives.
-Enhance technical skills relevant to statistics and programming.
-Need to manage/supervise small team/task.
-Need to focus on new business opportunities.
-Query resolution and other project support activities.
-Mentoring/Knowledge sharing in the project.
Eligibility Criteria:
Minimum 2+ years of experience in clinical trials space as a Statistical Programmer
Very good communication skills.
Postgraduation in Statistics**
Willingness to work in shifts.
Job Location : Noida( Delhi)
Interested candidates can email their resume to
Short-listed candidates will be called for an interview.
All the Best!
Tata Consultancy Services
Talent Acquisition Team
Shweta Shah
Experience 2 - 6 Years
Industry Type BPO/ITES
Role Bio-Statistician
Functional Area Healthcare, Medical, R&D
Location Mumbai, Mumbai Suburbs
Keywords Statistical programmer, Efficacy Table Figure Listing,Good clinical Practices,ICH guideline Protocol, CRF, SAP,clinical Trials Space
If you meet the above mentioned criteria, apply online
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