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Feasibility Specialist - Spain en Madrid

Descripción del empleo

PPD Spain are looking for Feasibility Specialist's to join our growing team.

In this role you will review RFP material (protocol and related documents), appraises new andcurrent business opportunities to include proposal planning and performs recruitment strategydevelopment and operational implementation.

Main Responsibilities

  • Performs feasibility assessment of clinical protocols to identify the best site selection strategy within the country and assess challenges of patient recruitment including the following responsibilities:
    • Develops recruitment funnel
    • Researches indication
    • Interviews Key Opinion Leaders, Patient Advocacy organizations, healthcare providers and site personnel
    • Generates questions to the sponsor regarding the opportunity
  • Lead engagement programs and meetings with PPD Select sites and Site Networking
  • Develop and maintain peer-to-peer collaborations and relationships with key medical experts in the community
  • Serve as scientific peer-to-peer resource to external disease experts and internal stakeholders
  • Assists in the development of patient recruitment programs across multiple therapeutic areas
  • Write supportive documentation to serve as basis for proposal assertions
  • Pulls Ad hoc requests from Sales including analysis and updates to prospective projects
  • Prepares and attends (in person or phone/web-based) client meetings in areas including bid defenses, screeners and recruitment materials development, investigator meeting, and other client meetings (as required)
  • Analyzes and works to continuously improve predictive performance metrics in support of activities focused on both business development and operations
  • Documents and tracks findings for future use
  • Assists in project start-up activities including:
    • Conducts internal handoff meeting
    • Generates internal database queries
    • Trains Acurian and site personnel on relevant aspects of protocol
    • Assists with creation or marketing material
  • Develops Screeners including the following functions:
    • Writes screener questions
    • Resolves Project Management or sponsor questions about screener
    • Works with IT to ensure correct programming of screener
    • Conducts call centre training session
    • Monitors screener performance after study launch
    • Utilizes existing Acurian template language and assist in development of new screener templates or processes
  • Pulls Ad hoc requests from Analytics, Project Management and IT other operational departments including analysis and updates to prospective or active projects

Documents, reports findings and makes recommendations to internal groups

Job Qualification:

Minimum Required Education and Experience:
  • Bachelor's degree in a life science related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
  • Previous experience that provides the knowledge, skills, and abilities to perform the job, comparable to 4+ years of experience as a clinical research monitor, experience in Thought Leader engagement programs and/or Patient Advocacy as Medical Science Liaison/Medical Affairs roles, and/or experience in peer-to-peer interaction and engagement with KOLs and proactive patient recruitment programs
  • Experience interacting directly with patients in a research setting is a plus
  • Valid driver's license where applicable.

Required Knowledge, Skills and Abilities:
  • Ability to analyze with strong attention to details and critical thinking
  • Persuasive communication and writing skills and the ability to simplify complex medical concepts
  • Strong organizational skills and ability to perform multiple tasks
  • Ability to work independently, function effectively as a member of a team and adhere to strict deadlines
  • Ability and willingness to work collaboratively across multiple teams (Sales, Analytics, Proposals, Project management, IT, Media, etc.). Strong working knowledge of (Word, Excel, PowerPoint) in a PC environment
  • Demonstrated comprehensive understanding of clinical research patient recruitment across multiple therapeutic areas. Working Conditions and Environment: Long, varied hours required occasionally

Pharmaceutical Product Development, LLC, the parent company of PPD Development, L.P. and Acurian,Inc. is firmly committed to Equal Employment Opportunity (EEO) and prohibits employmentdiscrimination for employees and applicants based on age, race, color, pregnancy, gender, genderidentity, sexual orientation, national origin, religion, marital status, citizenship, disability orprotected veteran or other status protected by federal, state, and/or local law.

Diversity Statement

PPD is proud to be an affirmative action employer that values diversity as a strength and fostersan environment of mutual respect. PPD is committed to providing equal employment opportunitieswithout regard to age, race, color, pregnancy, national origin, religion, sex, gender identity,sexual orientation, disability, veteran status or status within any other protected group.

This employer is a corporate member of myGwork, the business community for LGBTQ+ professionals, students, inclusive employers & anyone who believes in workplace equality.

Información extra

Estudios requeridos
Horas a la semana
8 - 40
Tipo de contrato
Tiempo completo
Tipo de trabajo
Marketing / Publicidad
Carnet de conducir
Carta de motivación

Madrid | Trabajo de marketing | Tiempo completo | Otros

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