**Clinical Operations Director - (RWE) Real World Evidence - Germany** - (1807797) in Berlin at IQVIA™

Date Posted: 6/25/2018

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    Berlin
  • Job Type:
    Statistics
  • Experience:
    3 to 5 years
  • Date Posted:
    6/25/2018
  • Job ID:
    1807797

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.

IQVIA™ (NYSE:IQV) 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.

We are seeking a line manager for Clinical Operations heading up two delivery teams consisting of scientists and programmers in Frankfurt am Main and Berlin, respectively. You will provide support to the teams and have operational accountability for retrospective/prospective non-interventional studies (NIS), interventional studies as well as disease registry management, while optimizing speed, quality and cost of delivery and in accordance with SOPs, policies and practices. In addition, you will contribute to the IQVIA organization in achieving the business objectives incl. budget responsibility.

Accepting this challenge, you will be joining a company that has industry-leading approaches to planning and conducting real-world studies and clinical trials, combining knowledge and experience with data-driven insights to make valuable contributions throughout the trial lifecycle.

Responsibilities

•  Conception and oversight of retrospective/prospective, non-interventional studies (NIS), interventional studies as well as registry set-up and management incl. budget responsibility

•  Providing support and expertise to your teams which are focused on medical writing, eCRF design, biostatistics, analytics and clinical study reports (CSR)

•  Manage both teams and foster collaboration across your teams as well as across the organization

•  Providing guidance on regulatory requirements incl. GCP, GPP and GVP

•  Working closely with key opinion leader, sponsors and clinical networks

•  Providing expert advises to the development of operationally sounded delivery strategies for small (1-2 country-) studies in partnership with sales and other functions responsible for business development activities



Job Requirements

Skills and Experience required

  • Robust and current knowledge of scientific, clinical, regulatory and commercial landscape in Germany, optimally combined with expertise in oncology
  • Excellent communication, presentation and interpersonal skills, including good command of German and English language (both written and spoken)
  • Strong business acumen
  • Ability to establish and maintain effective working relationships with excellent leadership skills
  • Master's degree in life sciences or equivalent combination of education, training and experience
  • Minimum of 3-5 years of experience of study management including team responsibility  

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: 1807797