Senior Director for Clinical Study

Qualification and Requirements

1. MD or PhD on oncology/immunology/another relevant field.
2. 5+ years clinical experience in cancer treatment, especially hemooncology and myeloma.
3. 5+ years experience in clinical studies management for oncology or cell therapy.
4. 5+ years experience in big pharma senior management working on clinical development and medical affairs.

Roles and Responsibilities

1. Lead a team in designing the clinical development strategy or plan for cancer therapeutics.
2. Work with local development and project teams at headquarters to run the development of local cancer therapeutics in Latam.
3. Oversee and manage medical and clinical operations, ensuring compliance with regulatory standards and ethical practices in Latam. Work together with the RA team to get marketing authorization in Latam for cancer therapeutics products.
4. Develop and implement comprehensive policies and procedures related to medical care tailored to meet the company’s needs, working with partners, hospitals, and medical organization in Latam;
5. Collaborate with other departments in the company, providing medical advice and consultation to executives and stakeholders.
6. Foster a culture of continuous quality improvement, monitoring key performance indicators and implementing initiatives to optimize healthcare delivery.
7. Lead interdisciplinary teams, encouraging collaboration, communication and knowledge sharing among medical professionals and staff.
8. Build and maintain strong relationships with key stakeholders, including medical associations, government bodies and community organizations, to promote healthcare initiatives and partnerships.