Medical Director - Baden-Württemberg, Deutschland - Full-Life Technologies

Beschreibung

Full-Life Technologies Limited ("Full-Life") is a fully integrated global radiotherapeutics company with operations in Belgium, Germany, and China. We seek to own the entire value chain for radiopharmaceutical research & development, production & commercialization in order to deliver clinical impact for patients. The Company plans to attack core issues affecting radiopharmaceuticals today through innovative research that targets the treatments of tomorrow. We are comprised of a team of fast-moving entrepreneurs and scientists with a demonstrated track record in the life sciences, as well as radioisotope research and clinical development. The team is expanding fast globally with more than 60 full-time employees now.

Full-Life had completed 3 rounds of equity financing with more than $110 million raise and an acquisition with a total transaction value of $245 million in the past year. Learn more at:

POSITION OVERVIEW:

The Medical Director role plays a critical role in overseeing the development and execution of oncology and radioisotope therapy programs within our biotech company. We are actively seeking a highly qualified candidate with expertise in nuclear medicine and/or radio-oncology, particularly in radiotherapy, and a proven track record in therapy methods. Experience working in hospital settings and proficiency in writing for regulatory submissions/institutional review boards are highly desirable qualifications for this role.

While experience in the pharmaceutical industry is beneficial, it is not mandatory. Candidates with a background in hospital-based radiotherapy or nuclear medicine are encouraged to apply.

ROLE & RESPONSIBILITIES:

• Provide medical leadership and medical monitoring of clinical trials.
• Provide strategic direction in the development and execution of oncology and radioisotope therapy programs.
• Oversee clinical trial design, implementation, and data analysis to ensure the safety and efficacy of therapies.
• Collaborate with cross-functional teams to develop and execute clinical development plans, including regulatory submissions.
• Serve as the primary medical liaison with key opinion leaders, regulatory agencies, and clinical trial investigators.
• Contribute to the development of medical education and training programs for internal teams and external stakeholders.
• Stay abreast of latest developments in oncology and nuclear medicine research and provide medical expertise to support business development activities.

SOFT SKILLS:

• Strong leadership and decision-making abilities.
• Ability to thrive in a fast-paced, dynamic environment.
• Excellent problem-solving and analytical skills.
• Adaptability and flexibility to changing priorities and deadlines.
• Commitment to maintaining the highest standards of medical ethics and patient care.
• Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external partners.

EXPERIENCE:

• Minimum of 3 years of relevant experience in oncology and nuclear medicine. Either in a hospital setting or in the pharmaceutical business.
• Demonstrated experience as physician in the radiotherapy field or in leading global clinical development programs.
• Understanding of regulatory requirements and experience with regulatory submissions (FDA).
• An experience in the conduct of Dosimetry trials would be a great plus.

EDUCATION:

• Medical degree (MD or equivalent) with specialization in oncology or nuclear medicine or a related field.
• Board certification in nuclear medicine or radiation oncology preferred.
• Fluent in written and spoken English; proficiency in additional languages is a plus.

PREFERRED INDUSTRY BACKGROUND:

Practitioner in hospital setting or pharmaceutical business.