WuXi AppTec

  • Oncology Clinical Research Associate - Future Projects

    Job Locations US-TX-Austin
    Job ID
    2018-4642
  • Overview

    Job Summary: The Clinical Research Associate II performs and coordinates aspects of the field-based and office-based monitoring and data quality control functions in accordance with Good Clinical Practices (GCP), International Conference on Harmonisation (ICH), and ResearchPoint Global SOPs. This can be a work from home position and requires approximately 50-75% travel.  

    Responsibilities

    Essential Job Functions:

    • Provides operational support for Clinical Operations
    • Performs field-based and in-house monitoring and site management tasks to assure conformance to current regulatory, ResearchPoint Global, and sponsor requirements
    • Performs data quality control functions including, but not limited to, query management and data audit functions
    • Participates in team and sponsor meetings and training programs, as required
    • Produces and maintains documentation of activities and findings as required by ResearchPoint Global and sponsor
    • Fiscal management of trip costs, positive feedback from site staff, low data error rates, complete and timely site monitoring, expense, and time sheet reporting
    • Position requires employee be aware of budget constraints for travel time, in-house and time at site and to manage to those constraints and to alert supervisor and project manager if they cannot be effectively managed
    • May provide informal guidance to more junior employees/contractors on project-specific tasks
    • Receives direct supervision from Project Managers, Clinical Managers or above
    • Receives daily project supervision from project managers and data managers
    • Must show ability to present solutions to issues; must show ability to apply previous lessons to future project work
    • Is expected to apply decisions from previous discussions to new situations and seek confirmation only
    • Must show ability to review regulatory documents in advance of Quality Assurance review with high level of accuracy and make decisions on the quality of the documents and take appropriate action
    • Must make effective decisions on managing tasks within time constraints so that deadlines are not missed
    • Expected to require supervision on issues that can have substantial impact on clinical, data quality, or regulatory issues
    • Works on routine assignments per written procedures, where ability to recognize deviation from accepted practice is required
    • Normally receives minimal instructions on routine work and detailed instructions on new assignments
    • Works under close supervision from supervisor or senior personnel
    • Ability to work in a team environment and independently as required

    Qualifications

    Job Requirements

     

    Experience / Education:         

    • Expected to have a minimum of 3 years related clinical research experience and a minimum of three months co-monitoring or co-auditing in the field or equivalent
    • Bachelor’s degree or HS diploma with commensurate experience
    • Preference given to those with CCRC, CCRA, CCRP certifications
    • Oncology / Critical Care experience preferred

     

    Knowledge / Skills / Abilities: 

    • Proficient skills with Microsoft Office Suite applications
    • Must have strong attention to detail and demonstrate understanding of the critical nature of ResearchPoint Global documentation 
    • Must have ability to initiate steps according to established processes without intervention
    • Must have ability to interact with internal and external customers and sites professionally, using clear diction
    • Must exhibit concise technical writing skills with minimal grammatical or logical errors
    • Ability to organize workload and handle multiple priorities
    • Must be able to solve problems independently when required and must be able to anticipate risks to the project within the scope of the position and to propose solutions to supervisor
    • Must have positive, professional demeanor with all interactions on the phone or in the office
    • Must have excellent verbal and written communication in English
    • Ability to work in team environment and effectively manage multiple priorities within established time constraints 
    • Expected to have knowledge of Good Clinical Practices; good working knowledge of physician care in hospitals, clinics, or other healthcare settings
    • Ability to work in satellite environment independently, but remain engaged with home office and supervisor
    • Ability to mentor staff
    • Travel is required 50-75% , primarily domestic/infrequently international, daily/overnight
    • Must have a valid driver’s license and the ability to rent a car

     

    Physical Requirements:                  

    • Must be able to travel
    • Must be able to work in an office or medical site
    • Ability to stand or sit for most of the work day
    • Must be able to perform some activities with repetitive motion, such as keyboarding
    • Must be able to travel for long distances in various methods of transportation (ie. car, airplane, shuttle bus, etc.)
    • Must be able to navigate to and from site locations, hotel, and airports with personal luggage and laptop
    • If working remotely must have access to high speed internet service and have knowledge and ability to resolve IT and computer related challenges through remote communications channels

     

    This job description does not state or imply that the above are the only duties and responsibilities assigned to this position.  Employees holding this position will be required to perform any other job-related duties as requested by Management.

     

    An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

     

     

     

     

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