NonStop Consulting
Our client, a leading name in clinical research operations, offers an exciting opportunity within their dynamic and supportive Germany ClinOps team. Committed to professional excellence, the company has a history of promoting motivation, teamwork, and independent work styles which support career advancement for employees. This organization is renowned for its innovative contributions to clinical operations, particularly in oncology projects, making it an ideal place for those looking to enhance their expertise in specialized research areas.
Company Description
Our client boasts a strong reputation for their comprehensive approach to clinical research. They value collaboration and knowledge sharing, empowering team members to grow their capabilities while working on high-impact clinical trials. Based in Germany, the ClinOps team prioritizes both professional development and the success of their clinical projects.
Benefits
– Be part of a collaborative team that values motivation and independent work styles, nurturing a culture of personal and professional growth.
– Engage in specialized oncology research projects, expanding your clinical research expertise in a highly valued field.
– Benefit from extensive travel opportunities, perfect for those who enjoy working in diverse environments and exploring new areas.
Role Responsibilities
– Conduct effective monitoring of clinical trials, contributing significantly to high-quality outcomes and furthering the company’s mission in advancing medical research.
– Collaborate with multiple clinical vendors, ensuring robust and efficient trial management and implementation of best practices.
– Utilize your electronic CRF and Office skills to manage project communications and document findings, driving the success of each clinical trial.
Requirements
– Hold a Bachelor’s degree in a related field, such as Life Sciences, and demonstrate 2-5 years of experience as a CRA/SCRA, particularly with a focus on oncology or epilepsia in clinical trials.
– Possess a strong understanding of ICH, GCPs, and local regulatory standards, ensuring compliance and excellence in all trial activities.
– Be fluent in both English and German, with a willingness to travel extensively across Germany for site visits (6-8 per month).
Closing Statement
If you are eager to take your clinical research career to new heights and join a team that values your growth, apply now to become an integral part of this thriving clinical operations division. Embrace the opportunity to work on groundbreaking research while expanding your professional horizons in Germany.
