• Contracts and Proposals Associate

    Job Locations US-PA-Plymouth Meeting, PA. USA
    Job ID
    Position Type
    Permanent Employee - Full-Time
  • Position Summary


    Primarily responsible for creating pricing and contracts for changes in scopes as well as for creating cost estimates for CRF Health's products and services. 


    • Completes basic pricing and Change in Scope requests, in coordination with other members of the Contracts and Proposals team
    • Works closely with project teams to determine appropriate terms and conditions of Changes in Scope
    • Coordinates with the company’s legal staff for review of all Change in Scope documents
    • Updates internal systems with pertinent budget and contract information on an ongoing basis
    • Coordinates the procurement of study specific hardware
    • Conducts QC of pipeline and forecast data in company spreadsheets and systems
    • Assists with administrative support duties as needed (i.e. overseeing of the contract signature and filing process, tracking of contracts and proposals activity) in Contracts Coordinator's absence
    • Other responsibilities assigned as required


    • Bachelor’s Degree is preferred, but not required
    • Minimum of intermediate Excel skills required
    • Basic understanding of contracting processes a plus
    • Pharmaceutical industry experience a plus
    • Must have excellent attention to detail, time management, communication, decision making, human relations, analytical skills, and organizational skills
    • Must be able to communicate effectively with all levels of the organization
    • Able to produce high quality work and to manage multiple competing tasks in a fast-paced environment
    • Must be a team oriented person with a “can do” attitude
    • Must be able to work effectively in a dynamic, fast-paced environment.


    About CRF Health

    Global Leader in eCOA Solutions for Clinical Trials 


    CRF Health is a global leader in eCOA (electronic Clinical Outcome Assessments) solutions for the life sciences industry. eCOA encompasses PROs (Patient Reported Outcomes), ObsROs (Observer Reported Outcomes) and ClinROs (Clinician or Rater Reported Outcomes) with outstanding project management focused on delivering value for our customers.  Committed to driving the change to higher quality outcomes and more efficient paper-free clinical trials through improved patient engagement, our intuitive and patient-focused eCOA technology helps companies bring new medicines to market quickly, safely and more cost-effectively. Our complete eCOA solutions are ideal for home and site-based phase I-IV clinical trials across the world for many therapeutic areas and patient populations.  More information to be found on our website.  


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