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**Clinical Operations Director - (RWE) Real World Evidence - Germany** - (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
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