Sign In
 [New User? Sign Up]
Mobile Version

Senior Biostatistician, Late Development Statistics

Merck


Location:
Upper Gwynedd, PA
Date:
08/16/2017
2017-08-162017-09-15
Job Code:
BIO004869
Merck
  •  
  • Save Ad
  • Email Friend
  • Print

Job Details

Job Title: Senior Biostatistician, Late Development Statistics  - BIO004869

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. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Merck is on a quest for cures and is committed to being the world’s premier, most research-intensive biopharmaceutical company. Today, we’re doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck’s leading discovery capabilities and world-class small molecule and biologics R&D expertise to create breakthrough science that radically changes the way we approach serious diseases. 

 
Responsibilities:

  • Develops, coordinates, and provides biostatistical support for related drug/vaccine projects under supervision in Late Development Statistics.
  • Interacts with Clinical, Regulatory, Statistical Programming, Data Management and other Merck Research Laboratories Scientists in designing and analyzing clinical trials, and in coordinating the statistical activities for clinical drug/vaccine projects.
  • The incumbent may initially work in a specific disease therapeutic area.

    Primary activities:
  • Serves as statistical representative in the cross-functional teams for the clinical trial planning, execution, and reporting.
  • Develops individual protocols and data analysis plans and determines appropriate statistical methodology for data analysis.
  • Participates in database design meetings to ensure that the data evaluated are in high quality and satisfy analysis requirements.
  • Collaborates with the statistical programming staff to ensure that all programs meet analysis requirements, internal standard operating procedures, and external regulatory requirements.
  • Evaluates appropriateness of available software for planned analyses and ascertains needs for potential program development of novel statistical methodology.
  • Analyzes data and interprets results from clinical trials to meet objectives of the study protocol. Independently applies and implements basic and complex techniques to these analyses.
  • Prepares oral and written reports to effectively communicate results of clinical trials to the project team, management, regulatory agencies, or individual investigators.
  • Provides responses to queries relating to study design, analysis, and interpretation posed by the clinical monitors, regulatory agencies, and/or investigators.
  • Is responsible for planning and ensuring the accuracy of Statistical Review Aids submitted to regulatory agencies.
  • Participates with management in discussions with corresponding scientific personnel at regulatory agencies and with investigators concerning proposed or ongoing studies.
  • Involved in research activities for innovative statistical methods and applications in clinical trial development


Qualifications

Education:

  • PhD or equivalent degree in statistics/biostatistics or related discipline, or a Master’s degree with a minimum of 3 years relevant experience.

Required:

  • Knowledge of statistical analysis methodologies and experimental design.
  • Working knowledge of statistical and data processing software e.g. SAS and/or R.
  • Good oral and written communication skills. Able to work effectively with personnel with different functional background.
  • Demonstrate strong interest in statistical research activities and in application of novel methods to clinical trial development.
  • Must also demonstrate the ability to learn, be proactive and motivated, and consistently focus on details and execution.

Preferred:

  • An understanding of biology of disease and drug discovery and development.

 

Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. 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.

 

For more information about personal rights under Equal Employment Opportunity, visit:

 

            

            



Job Biostatistics

Primary Location NA-US-PA-Upper Gwynedd

Other Locations NA-US-NJ-Rahway

Employee Status Regular

Number Of Openings 2

Powered By

Featured Jobs[ View All ]