Job Description

Job Description

Company Description

Curtana Pharmaceuticals is a pioneering early clinical-stage biopharmaceutical company dedicated to developing transformative, first-in-class therapies for the most aggressive forms of brain cancer. Headquartered in Austin, Texas, our mission is to address the urgent unmet medical needs of patients with glioblastoma, medulloblastoma, DMG/DIPG and other brain cancers. Our lead candidate, CT-179, an OLIG2 inhibitor, has shown significant promise in preclinical studies and has received FDA Orphan Drug Designation, Rare Pediatric Disease Designation, and Fast Track Designation. We are a passionate and collaborative team, driven by a commitment to scientific excellence and a desire to make a meaningful impact on the lives of patients.

Position Summary

We are seeking a highly experienced and strategic Chief Medical Officer (CMO) to join our team on a part-time basis. The CMO will be a key member of the executive leadership team and will be responsible for providing medical and clinical leadership for the company's development programs. The successful candidate will have a proven track record of designing and executing early-stage oncology clinical trials in both the US and Australia. This is an exceptional opportunity to play a pivotal role in the growth and success of a dynamic and innovative biopharmaceutical company.

Key Responsibilities

• Provide strategic leadership and oversight for all clinical development activities, including clinical trial design, implementation, and execution.
• Lead the development of clinical trial protocols, investigator brochures, and other regulatory documents.
• Serve as the primary medical monitor for all clinical trials, ensuring patient safety and data integrity.
• Establish and maintain strong relationships with key opinion leaders, investigators, and clinical trial sites.
• Provide medical and scientific input to support regulatory submissions and interactions with health authorities in the US and Australia.
• Contribute to the development and execution of the company's overall corporate strategy.
• Represent the company at scientific conferences, investor meetings, and other external events.

Qualifications and Experience

• MD with a board certification in oncology or a related specialty.
• Experience in neuro-oncology and pediatric oncology is highly desirable.
• Extensive experience in designing and conducting early-stage (Phase 1 and 2) oncology clinical trials is required.
• Demonstrated experience with clinical trial operations in both the United States and Australia is mandatory.
• Strong understanding of GCP, ICH guidelines, and other regulatory requirements for clinical trials.
• Excellent leadership, communication, and interpersonal skills.
• Ability to work effectively in a fast-paced, entrepreneurial environment.

Preferred Qualifications

• MD with board certification in neuro-oncology or pediatric neuro-oncology.
• Experience with regulatory submissions (INDs, NDAs) to the FDA and other health authorities.
• A strong network of contacts within the oncology clinical research community.
• Experience in a small biotech or pharmaceutical company environment.

Job Tags

Similar Jobs