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Senior Statistical Programmer. Job in Upper Gwynedd, Pennsylvania, United States in Merck & Co., Inc.. Nelest.com
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Senior Statistical Programmer

col-narrow-left   

Job ID:

22191

Location:

Upper Gwynedd, PA 

Job function:

Information Systems Management
col-narrow-right   

Posted:

03.05.2016

Employment Type:

Full time

Industry:

Healthcare / Pharma
col-wide   

Title:

Senior Statistical Programmer

Job Description:

Description Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Reporting to Director of Analysis and Reporting Standards, Statistical Programming, the incumbent supports the design, development, and delivery of efficient, flexible, and modular analysis and reporting and submission code standards that can be used for drug and/or vaccine projects across all therapeutic areas. Adheres to standard operating procedures and guidelines established by the department. Drives data structures (analysis and reporting data standards and submission standards) and actively contributes to the department's strategic initiatives. Travel: Yes, 5 % of the Time Description Senior Statistical Programmer-STA000739 Description Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Reporting to Director of Analysis and Reporting Standards, Statistical Programming, the incumbent supports the design, development, and delivery of efficient, flexible, and modular analysis and reporting and submission code standards that can be used for drug and/or vaccine projects across all therapeutic areas. Adheres to standard operating procedures and guidelines established by the department. Drives data structures (analysis and reporting data standards and submission standards) and actively contributes to the department's strategic initiatives.? Qualifications Education:
  • Bachelor's degree (Masters preferred) in Computer Science, Statistics, Life Sciences or related field.?

Job Requirements:

Qualifications Education:
  • Bachelor's degree (Masters preferred) in Computer Science, Statistics, Life Sciences or related field.?

Required: ?????
  • BA/BS plus a minimum of 5 years or MS plus a minimum of 3 years SAS programming experience in clinical trials setting
  • Thorough knowledge of programming techniques in SAS and familiarity with at least one other statistical computing software
  • Knowledge and experience in developing analysis and reporting statistical programming deliverables (datasets, statistical analyses, tables, listings and figures) for research and development projects
  • Knowledge and understanding of CDISC SDTM and ADaM analysis dataset standards
  • Experience with SAS macro language, various SAS procedures, and/or SAS GRAPH
  • Experience working with analytical research databases including various analysis datasets and procedures
  • Demonstrated understanding of statistics, clinical trial, and data management concepts as applied to drug/vaccine development
  • Excellent communication, interpersonal, and negotiation skills with a demonstrated history of teamwork and ability to communicate and collaborate effectively

Preferred:
  • R and/or XML experience
  • Experience with SAS in Unix
  • Experience in developing flexible and efficient complex analysis and reporting standard SAS macros







Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com. Search Firm Representatives Please Read Carefully: Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster EEOC GINA Supplement? Merck is an equal opportunity employer, Minority/Female/Disability/Veteran - proudly embracing diversity in all of its manifestations.

Zip Code:

19446

Company Info
Merck & Co., Inc.

Kenilworth, NJ, United States

Phone:
Web Site: merck.com

Company Profile

Company Info


Merck & Co., Inc.
Kenilworth, NJ, United States
Phone:
Web Site: merck.com

Senior Statistical Programmer

col-narrow-left   

Job ID:

22191

Location:

Upper Gwynedd, PA 

Job function:

Information Systems Management
col-narrow-right   

Posted:

03.05.2016

Employment Type:

Full time

Industry:

Healthcare / Pharma
col-wide   

Title:

Senior Statistical Programmer

Job Description:

Description Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Reporting to Director of Analysis and Reporting Standards, Statistical Programming, the incumbent supports the design, development, and delivery of efficient, flexible, and modular analysis and reporting and submission code standards that can be used for drug and/or vaccine projects across all therapeutic areas. Adheres to standard operating procedures and guidelines established by the department. Drives data structures (analysis and reporting data standards and submission standards) and actively contributes to the department's strategic initiatives. Travel: Yes, 5 % of the Time Description Senior Statistical Programmer-STA000739 Description Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Reporting to Director of Analysis and Reporting Standards, Statistical Programming, the incumbent supports the design, development, and delivery of efficient, flexible, and modular analysis and reporting and submission code standards that can be used for drug and/or vaccine projects across all therapeutic areas. Adheres to standard operating procedures and guidelines established by the department. Drives data structures (analysis and reporting data standards and submission standards) and actively contributes to the department's strategic initiatives.? Qualifications Education:
  • Bachelor's degree (Masters preferred) in Computer Science, Statistics, Life Sciences or related field.?

Job Requirements:

Qualifications Education:
  • Bachelor's degree (Masters preferred) in Computer Science, Statistics, Life Sciences or related field.?

Required: ?????
  • BA/BS plus a minimum of 5 years or MS plus a minimum of 3 years SAS programming experience in clinical trials setting
  • Thorough knowledge of programming techniques in SAS and familiarity with at least one other statistical computing software
  • Knowledge and experience in developing analysis and reporting statistical programming deliverables (datasets, statistical analyses, tables, listings and figures) for research and development projects
  • Knowledge and understanding of CDISC SDTM and ADaM analysis dataset standards
  • Experience with SAS macro language, various SAS procedures, and/or SAS GRAPH
  • Experience working with analytical research databases including various analysis datasets and procedures
  • Demonstrated understanding of statistics, clinical trial, and data management concepts as applied to drug/vaccine development
  • Excellent communication, interpersonal, and negotiation skills with a demonstrated history of teamwork and ability to communicate and collaborate effectively

Preferred:
  • R and/or XML experience
  • Experience with SAS in Unix
  • Experience in developing flexible and efficient complex analysis and reporting standard SAS macros







Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com. Search Firm Representatives Please Read Carefully: Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster EEOC GINA Supplement? Merck is an equal opportunity employer, Minority/Female/Disability/Veteran - proudly embracing diversity in all of its manifestations.

Zip Code:

19446
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