Senior Director for Clinical Study Management
2 meses atrás
Qualifications and Requirements
We are seeking a highly experienced and skilled professional to join our team at Sinovac Biotech Ltd. as a Senior Director for Clinical Study Management. The ideal candidate will have a strong background in oncology, immunology, or a related field, with a minimum of 5 years of clinical experience in cancer treatment, particularly in hematology and myeloma.
The successful candidate will also have a proven track record of managing clinical studies in oncology or cell therapy, as well as experience in senior management roles within the pharmaceutical industry.
Key Responsibilities
- Lead a team in designing and implementing clinical development strategies for cancer therapeutics.
- Collaborate with local development and project teams to run the development of local cancer therapeutics in Latin America.
- Oversee and manage medical and clinical operations, ensuring compliance with regulatory standards and ethical practices in Latin America.
- Work with the Regulatory Affairs team to obtain marketing authorization in Latin America for cancer therapeutics products.
- Develop and implement comprehensive policies and procedures related to medical care, tailored to meet the company's needs, in collaboration with partners, hospitals, and medical organizations in Latin America.
- Provide medical advice and consultation to executives and stakeholders across the organization.
- Foster a culture of continuous quality improvement, monitoring key performance indicators, and implementing initiatives to optimize healthcare delivery.
- Lead interdisciplinary teams, promoting collaboration, communication, and knowledge sharing among medical professionals and staff.
- Build and maintain strong relationships with key stakeholders, including medical associations, government bodies, and community organizations, to promote healthcare initiatives and partnerships.
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