Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment. From the Clinical Operations department we are looking for a Clinical Operations Specialist who will be responsible for supporting the successful execution of clinical studies for all Bioscience products, following ICH-GCP guidelines and all applicable regulatory requirements.
What your responsibilities will be You will report to the Clinical Operations Manager to align business needs and priorities and meet company goals and objectives. You will develop and improve Clinical Operations processes to increase the department efficiency and quality standards. You will communicate and work with other functional groups to identify, review, maintain, align and improve cross-functional processes throughout the clinical programs. You will interact with the Clinical Operations department staff and project teams to provide guidance to resolve compliance issues. You will be involved in tasks and decisions related to the development of new technologies for the Clinical Operations department. You will ensure compliance with GCP/ICH and regulatory guidelines. Who you are To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions).
You have a Life Sciences Degree and/or Master. You have at least 3 years of experience in clinical trials (site monitor or CRA preferred). You speak and write English fluently. You have a knowledge of ICH GCPs, FDA, EMA and CFRs regulatory requirements and understanding of continuous change in the regulatory environment. You are familiar with Clinical Operations processes, systems and SOPs, needed for the conduct of a clinical study. You like to communicate with your colleagues and the other departments and you feel comfortable in environments where flexibility and dynamism is required. You are highly detail-oriented and you are a person with good organization and time-management skills. What we offer It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.
Information about Grifols is available at www.grifols.com. If you are interested in joining our company and you have what it takes for such an exciting position, then don't hesitate to apply!
We look forward to receiving your application!
Grifols is an equal opportunity employer.
Flexibility for U Program: Hybrid Model
Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h.
Benefits package Contract of Employment: Temporary position
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