Senior Regulatory Operations Associate- Document Processing

Location
Cambridge
Salary
See job description.
Posted
November 18 2020
Ref
R0015760
Position Type
Full Time
Organization Type
Pharma
Job Type
Staff Scientist


Senior Regulatory Operations Associate- Document Processing
United Kingdom - Cambridge

Gilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Gileads therapeutic areas of focus include HIV/AIDS, liver diseases, cancer and inflammation, and serious respiratory and cardiovascular conditions.

Making an impact on a global scale
Inclusion is one of the companys five core values. Thats because we know that we are stronger and more innovative at Gilead when we are informed by a diverse set of backgrounds, experiences and points of view. Gilead Sciences is a biopharmaceutical company that discovers, develops and commercializes innovative therapeutics in areas of unmet medical need. The company's mission is to advance the care of patients suffering from life-threatening diseases worldwide.

When you join Gilead, you join our mission to change the world by enabling people to live healthier and more fulfilling lives. Come join a mission-driven bio-pharmaceutical organization that values inclusion and diversity, has a strong portfolio of products, and is constantly #CreatingPossible


Role Overview / Summary
  • Routine and complex document formatting and report processing of all types with little supervision and involvement by manager.
  • Adopts responsibility for document processing activities occurring under their guidance.


Job Responsibilities
  • Prepares a variety of routine and non-routine Word and PDF formatting including utilization of Document Processing supporting tools for submission-ready documentation.
  • Performs filing and data retrieval functions as directed, or in conjunction with departmental SOPs.
  • Participates in supporting and promoting current routine electronic initiatives in moving the company forward with electronic submissions and electronic archives.
  • Confident interface with projects managers, regulatory product managers, and or content authors to discuss routine and non-routine documentation preparation and content.
  • May take significant responsibilities in submission planning meetings to become familiar with the submission priorities.
  • Performs workflows and procedures regarding document tracking, indexing, retrieving and disseminating of regulatory agency submissions as defined by Regulatory Operation management.
  • Carries out project tasks under the direction of manager. Provides the status of their ongoing projects and Document Processing activities to the manager when required.
  • Provide training to others on software tools used and educating authors on Document Processing procedures and submission-ready requirements.
  • Leads projects of high complexity. Makes independent and appropriate decisions. May lead cross-functional projects and represent Reg Ops at project meetings. Proactively communicates the status of ongoing projects and submissions to the manager, and suggests solutions to problems.


Knowledge & Skills Required
  • Demonstrates continued success leading, involving regular Word and PDF formatting, with high-quality work output that requires minimal supervision.
  • Expert technical knowledge of current systems (Word, Acrobat, document management system, Document Processing supporting tools)
  • Demonstrates knowledge of how system implementations work.
  • Demonstrates strong project management skills, with the ability to manage the tasks of more junior associates.
  • Demonstrates a deep understanding of requirements for documentation sent to agencies by Gilead
  • A consistent demonstration of attention to detail, timeliness, and accuracy is critical.
  • Must be able to balance multiple tasks simultaneously to achieve goals and satisfy customers.
  • Works under limited direction and may independently determine and develop approaches to non-routine problems.


Education & Experience
  • BA, BS or MS and / or substantial relevant experience
  • Relevant experience includes electronic document management systems, global regulatory submissions, or other experience directly related to Regulatory Operations.


Equal Employment Opportunity (EEO)
It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual's gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.


For Current Gilead Employees and Contractors:

Please log onto your Internal Career Site to apply for this job.


To apply, visit https://gilead.wd1.myworkdayjobs.com/en-US/gileadcareers/job/United-Kingdom---Cambridge/Senior-Regulatory-Operations-Associate--Document-Processing_R0015760-2





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