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Are you an experienced Clinical Research professional with a passion for leading and developing teams? Are you ready for the next step in your career? We are looking for a Clinical Research Associate Line Manager to join our team in the Clinical-Medical-Regulatory & Quality department at Novo Nordisk. If you are ready to make a difference in the field of clinical research, read on and apply today for a life-changing career.
The position As a Clinical Research Associate Line Manager at Novo Nordisk, you will have the opportunity to: Manage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meet the project objectives. Provide line management and oversight to Novo Nordisk CRAs and CTAs staff under your reporting line. Continuously evaluate performance and individual learning & development needs against role expectations. Hire, onboard, and integrate new employees. Identify quality risks and issues and create appropriate corrective action plans. Conduct co-monitoring visits for coaching and sign-off for new monitors. Organize and attend meetings with CRO vendors. Identify and engage with new sites and investigators in new therapeutic areas. Conduct the evaluation of study feasibility. Qualifications
To be successful in this role, you should have the following qualifications:
Bachelor or other degree in Life Sciences or equivalent, e.g., medicine, pharmacy-biochemistry, biology, among others. Experience from a similar position in the pharmaceutical industry or Clinical Research Organization (CRO). Minimum 5 years of experience in clinical research. 2 years' experience as a Team Manager in clinical trials. Advanced English and Spanish (written and spoken). About the department
The Clinical-Medical-Regulatory & Quality department at Novo Nordisk is responsible for running all clinical development activities from initial planning of clinical trials towards authority submission. We investigate patients' reactions to new drugs, compare them to existing products, and run a set of trials in human beings. Our team provides resources, processes, and competencies in Biostatistics and Programming, Clinical Reporting, Data Management, Epidemiology/Real World Evidence, and Clinical Pharmacology to all development projects. We strive to align processes, develop competencies, and share knowledge to ensure the successful planning and execution of clinical trials.
Working at Novo Nordisk
Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we're working toward something bigger than ourselves, and it's a collective effort. Join us! Together, we go further. Together, we're life changing.
Contact
To complete your application, click on "Apply now", attach your CV in English and follow the instructions.
Deadline
Please apply before July 4th, 2024. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds, and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in.
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