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*Site ID Services Specialist 1 or 2 (f/m) - office-based or home-based in Germany, 12 month fixed term contract* (R1059392) in Frankfurt, DE at IQVIA™

Date Posted: 2/9/2019

Job Snapshot

  • Employee Type:
  • Location:
    Frankfurt, DE
  • Experience:
    Not Specified
  • Date Posted:
  • Job ID:

Job Description

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

Currently we are hiring a Site ID Services Specialist 1 or 2 (f/m) on a 12 month fixed-term contract, in part-time preferrable 32h/week, to work office-based in one of our offices in Frankfurt, Freiburg/Br. or München-Sauerlach or to work home-based throughout Germany. In this role you will manage and lead activities associated with Site Identification for regional and/or country projects and/or programs.

While projects vary, your typical responsibilities might include:

  • Manage assigned opportunities, projects, programs for country or region and adhere to timelines and budget.
  • Generate site list of appropriate investigators in accordance with the needs of the sponsor and specifications of the protocol
  • Coordinate collection and analysis of country / regional Site Identification information to meet timelines of proposal process
  • Reconcile and interpret Site Identification data to provide country level assessments and recommendations for country site numbers, recruitment rates, timelines and screen failure rates
  • Distribute, track, negotiate and review the Confidential Disclosure Agreements (CDAs) for Site Identification with assistance from Management / Legal department as appropriate
  • Distribute, track and review Site Questionnaire Forms for Site Identification for completeness, site capability and suitability of investigators
  • Manage the investigator database entry and quality, ensuring complete investigator and site information is captured, and monitor for duplicate entries
  • Maintain and update company information repositories and databases

You should have:

  • A degree in life sciences or related field
  • About 2-4 years’ relevant experience including demonstrable experience in acting as the main local lead in studies or equivalent combination of education, training and experience.
  • Fluent language skills in German and very good English language skills.
  • Sound knowledge of medical terminology, GCP, FDA regulations, and Drug Development process and procedures.
  • Strong communication, organizational and interpersonal skills.
  • Proficient in the use of Microsoft Office, Presentation skills and team training.
  • Ability to work independently, prioritize actively, seek input, problem solve and work in a team environment.
  • Strong negotiation skills.
  • Ability to handle multiple tasks with varying deadlines.
  • Ability to maintain confidentiality. 
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™

Job ID: R1059392