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Manual Encoding Lead - United States  

Company managed [?] Still accepting applications
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Posted on : 09 June 2017

Project Description

  • Our company 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 our company  has codified its 125-year legacy.
  • Our company’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
  • Our company 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. 
  • Our company  Research Laboratories is a true scientific research facility of tomorrow, and will take our company'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.
  • Under the direction of the applicable management, the Manual Encoding Lead (ME Lead) is responsible for executing end to end data management activities pertaining to the encoding of clinical trial data, including but not limited to: data management tool and system development, validation and maintenance, data collection, data integrity review and reconciliation, query management, medical coding, and database lock preparation, in compliance with company Standard Operating Procedures (SOPs) and ICH-GCP guidelines.
  •  Works with management to maintain the consistent execution of quality global procedures and monitors workload and resource allocation.
  •  Supports the comprehensive development of junior staff and encourages effective interaction of  GDO staff with business partners to achieve common objectives. 
  • Is accountable for the quality and timely execution and delivery of Global Data Operations (GDO) deliverables  related to encoding at the trial  and program level.

Primary activities include, but are not limited to:
  • All activities of an Encoder.
  •  Accountable for all encoding related protocol level start-up, in-life and database lock tasks and activities performed by all coding staff at the trial level.
  •  Interact and communicate with customers and stakeholders both internal and external to GDMS as well as company when needed.
  •  Accountable within GDO to design, create, validate, review, approve and maintain encoding  specifications as needed.
  •  Coordinate the execution of user acceptance testing of encoding as needed.
  •  Participate in relevant operational meetings.
  •  Execute and trigger communications and escalations at the protocol level within department, within function and cross-functionally.
  •  Execute and maintain adherence to a metrics control plan and quality assessment indicators at the trial level.
  •  Coordinate the database lock activities related to encoding and triage and track issues to resolution.
  •  Accept and execute special responsibilities related to process maintenance, data quality assessment, staff training and mentoring and/ or other special activities, such as developing and delivering programs and materials to instruct staff regarding business processes, leading or participating in cross functional technical improvement projects, etc.
  •  Continually monitor for opportunities to improve efficiency, effectiveness and quality and implement changes as appropriate at the trial level, program level, TA level and GDO Level.
  •  Performs tasks with minimal guidance from manager(s).
  •  Serve as subject matter expert for encoding processes, globally and locally, at the trial level, program level and TA Level.

B.A. or B.S. degree, preferably in Medicine, Pharmacy, Nursing, Biological Sciences, or health care related discipline

  •  Five years’ experience in Pharmaceutical Encoding and/or Vocabulary Management.
  •  Excellent Oral and written English language skills.
  •  Knowledge of regulations and policies applicable to the pharmaceutical industry encoding.
  •  Proficient overall working knowledge of the clinical development process and the value of encoding.
  •  Excellent working knowledge of clinical practice and medical terminology.

  •  Ability to work cross functionally and as part of a team.
  •  Be able to work under pressure in a changing environment with flexibility.
  •  Ability to work independently and accept and act with appropriate accountability with minimal guidance by a manager.
  •  Ability to coordinate the work of others and influence decision making.
  •  Exceptional communication skills (oral and written) with the ability to communicate with both the technical and business areas.
  •  Exceptional organizational, problem-solving and negotiating skills.
  •  Demonstrated excellent project management and leadership skills.

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. 

Travel: Yes, 5 % of the Time
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