- Lead the medical aspects of clinical studies, ensuring adherence to rigorous scientific and regulatory standards.
- Participate in regulatory project teams to ensure the highest quality of submissions to Regulatory Authorities.
- Maintain and expand the client's scientific and development network within the oncology space, fostering relationships with key stakeholders.
- Act as the safety responsible person, prioritizing patient safety throughout the drug development process.Qualifications:
- Medical Doctor degree is mandatory, combined with a PhD is a plus.
- Extensive experience in leading late-stage clinical development, including phase 3 programs.
- Experience in oncology or related therapeutic areas is preferred.
- Proven experience in interacting with Regulatory Authorities, ideally both EMA & FDA.
- Excellent analytical and communication skills in English and preferably in the native language.Why Choose Us:
- Join a dynamic and collaborative team dedicated to advancing healthcare and improving patient outcomes.
- Opportunities for professional growth and development within a leading Contract Research Organization.
- Work in a supportive environment that values innovation, integrity, and excellence.
- Competitive compensation and benefits package.
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Clinical Medical Director - Søborg, Danmark - TFS HealthScience
for 1 uge siden
Beskrivelse
Are you passionate about making a difference in the lives of patients with rare oncology diseases? Join our innovative team at TFS HealthScience as we expand our horizons and contribute to groundbreaking advancements in healthcare.
This position is sponsored-based in Sweden, but can work remote.
About Us:
TFS HealthScience is a leading mid-sized Contract Research Organization (CRO) dedicated to partnering with biotechnology and pharmaceutical companies throughout their clinical development journey. With a focus on excellence and innovation, we strive to deliver high-quality solutions that make a difference in patients' lives.
About the Opportunity:
The Clinical Medical Director will play a pivotal role in driving the development of life-changing treatments for rare oncology diseases. Reporting to the Chief Scientific Officer (CSO), this individual will provide strategic clinical development insights and lead the planning, delivery, and management of clinical development plans to advance the client's drug candidates.
Key Responsibilities: