Clinical Trial Scientist – Cardiovascular – Phase III

Our client, a dynamic pharmaceutical company based in Basel, Switzerland, is currently seeking a highly skilled and experienced Clinical Trial Scientist to join their Clinical Science and Operations team. With a global impact on healthcare, this role offers the chance to engage in innovative clinical science and operations within a collaborative and challenging environment.

Benefits

• Engage in cutting-edge research, contributing to cross-functional initiatives that impact healthcare on a global scale.
• Access opportunities for professional development, enhancing your skills and knowledge in a collaborative and challenging environment.
• Join a dynamic pharmaceutical company that values innovation and offers a global platform to make a difference in patients’ lives.

Responsibilities

• Collaborate closely with the Clinical Trial Physician (CTP) on relevant trial-related activities, serving as a core member of the clinical trial team.
• Develop a sound understanding of the science and medicine related to the trial, performing literature searches to keep knowledge up to date.
• Contribute to trial-level activities, including the development of clinical trial protocols, study committee charters, and subject narratives.
• Provide scientific input into responses for regulatory bodies and participate in discussions with external experts.
• Coordinate/manage study committees, perform data review and medical monitoring during the trial, and provide scientific training to relevant functions and roles.
• Contribute to cross-functional and clinical development initiatives and processes as needed.

Requirements

• PhD, Pharm D, MSc, or equivalent university degree in life or health sciences.
• Minimum 5 years of experience in a similar position, with at least 2 years in clinical development.
• Proficiency in working in a cross-functional environment, able to coordinate cross-functional activities.
• Previous experience in planning, conducting, and reporting phase II and III clinical studies from a scientific perspective is preferred.
• Fluency in English, both written and oral.

Do you have any disability or condition that could affect you in the application and interview process? Please feel free to share this information as part of your application, including any necessary adjustments you might need, so we can help make the process easier for you. We assure you this information will not have any negative effect on the interview process outcome.

About NonStop

We are NonStop, a leading provider of staffing solutions throughout Europe and now also in the US. We’re passionate about connecting talent with opportunity and work non-stop to support our clients in hiring the best talent for their teams. Feel free to pop over to our website, NonStop Consulting (https://www.nonstopconsulting.com), for more information, to browse all our roles, or to let us know how we can help you.