Clinical Oncology Research Physician

About Krystal Bio: At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs.

Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient’s end-to-end experience.

Krystal received U.S. FDA approval for the first and only redosable gene therapy treatment, VYJUVEK, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology.

Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan. We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members that embody these values.

Position Overview:

Krystal Biotech, Inc is seeking a board-certified Physician to support clinical development of innovative gene therapy applications, in the field of oncology. The Research Physician will work closely with cross-functional teams to design and execute clinical trials, ensuring scientific rigor and patient safety throughout the process. This position requires a deep understanding of oncology and clinical research, as well as a commitment to advancing treatment options for cancer patients through cutting-edge gene therapy approaches. This role will be based full-time at our Headquarters in Pittsburgh, PA.

Key Responsibilities:

• Serve as the principal medical expert for oncology clinical trials, monitoring patient safety, treatment efficacy, and compliance with regulatory guidelines
• Support the clinical development strategy for oncology-focused gene therapies, ensuring alignment with Krystal Biotech’s overall research and development goals
• Oversee clinical trials, including protocol development, patient selection, and endpoint determination
• Collaborate with internal teams and external stakeholders (clinical sites, CROs, key opinion leaders) to ensure seamless execution of clinical trials
• Analyze and interpret clinical trial data, preparing comprehensive reports for regulatory submissions, publications, and presentations
• Provide medical oversight during trials, addressing any clinical questions or concerns related to patient care or trial protocols
• Stay informed on the latest advancements in oncology, gene therapy, and clinical research, applying this knowledge to optimize trial design and outcomes
• Contribute to scientific publications, conference presentations, and other communications to share trial results and scientific insights
• Support regulatory submissions and communications with the FDA, EMA, and other regulatory bodies as needed
  
  

Qualifications:

• MD or equivalent with board certification in Oncology or Hematology-Oncology
• Clinical research experience in oncology
• Demonstrated knowledge of clinical trial design, management, and data interpretation.
• Familiarity with gene therapy or other advanced therapeutic platforms in oncology is highly desirable
• Knowledge of oncology biomarkers, immuno-oncology, or precision medicine is a plus
• Experience collaborating with global regulatory agencies and contributing to IND/NDA submissions, highly preferred
• Strong understanding of GCP, FDA, and EMA regulations related to oncology clinical trials
• Ability to work effectively within cross-functional teams and manage multiple priorities
• Excellent communication, leadership, and organizational skills
  
  

Krystal Biotech, Inc. is an Equal Employment Opportunity and Affirmative Action Employers. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. Headhunters and recruitment agencies may not submit resumes/CVs through this Web site or directly to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes. Krystal Biotech, Inc. will not pay fees to any third-party agency or company that does not have a signed agreement with Krystal Biotech, Inc.

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About Krystal Bio: At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs.

Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient’s end-to-end experience.

Krystal received U.S. FDA approval for the first and only redosable gene therapy treatment, VYJUVEK®, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology.

Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan. We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members that embody these values.

Position Overview:

Krystal Biotech, Inc is seeking a board-certified Physician to support clinical development of innovative gene therapy applications, in the field of oncology. The Research Physician will work closely with cross-functional teams to design and execute clinical trials, ensuring scientific rigor and patient safety throughout the process. This position requires a deep understanding of oncology and clinical research, as well as a commitment to advancing treatment options for cancer patients through cutting-edge gene therapy approaches. This role will be based full-time at our Headquarters in Pittsburgh, PA.

Key Responsibilities:

• Serve as the principal medical expert for oncology clinical trials, monitoring patient safety, treatment efficacy, and compliance with regulatory guidelines
• Support the clinical development strategy for oncology-focused gene therapies, ensuring alignment with Krystal Biotech’s overall research and development goals
• Oversee clinical trials, including protocol development, patient selection, and endpoint determination
• Collaborate with internal teams and external stakeholders (clinical sites, CROs, key opinion leaders) to ensure seamless execution of clinical trials
• Analyze and interpret clinical trial data, preparing comprehensive reports for regulatory submissions, publications, and presentations
• Provide medical oversight during trials, addressing any clinical questions or concerns related to patient care or trial protocols
• Stay informed on the latest advancements in oncology, gene therapy, and clinical research, applying this knowledge to optimize trial design and outcomes
• Contribute to scientific publications, conference presentations, and other communications to share trial results and scientific insights
• Support regulatory submissions and communications with the FDA, EMA, and other regulatory bodies as needed
  
  

Qualifications:

• MD or equivalent with board certification in Oncology or Hematology-Oncology
• Clinical research experience in oncology
• Demonstrated knowledge of clinical trial design, management, and data interpretation.
• Familiarity with gene therapy or other advanced therapeutic platforms in oncology is highly desirable
• Knowledge of oncology biomarkers, immuno-oncology, or precision medicine is a plus
• Experience collaborating with global regulatory agencies and contributing to IND/NDA submissions, highly preferred
• Strong understanding of GCP, FDA, and EMA regulations related to oncology clinical trials
• Ability to work effectively within cross-functional teams and manage multiple priorities
• Excellent communication, leadership, and organizational skills
  
  

Krystal Biotech, Inc. is an Equal Employment Opportunity and Affirmative Action Employers. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. Headhunters and recruitment agencies may not submit resumes/CVs through this Web site or directly to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes. Krystal Biotech, Inc. will not pay fees to any third-party agency or company that does not have a signed agreement with Krystal Biotech, Inc.

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