Perspective Therapeutics

Game-changing therapies that make an impactful difference for cancer patients and the clinicians who treat them.

Senior Director, Clinical Development

Program ManagerProgram ManagerFull TimeRemoteTeam 51-200Since 2023H1B No SponsorCompany SiteLinkedIn

Location

United States + 180 moreAll locations: United States, Canada, Brazil, Colombia, Argentina, Chile, Venezuela, Bolivarian Republic Of, Bolivia, Plurinational State Of, Ecuador, French Guiana, Guyana, Paraguay, Peru, Suriname, Uruguay, Mexico, Costa Rica, El Salvador, Guatemala, Honduras, Nicaragua, Panama, Dominican Republic, Puerto Rico, Bahamas, Guadeloupe, Haiti, Jamaica, Martinique, Montserrat, United Kingdom, Germany, France, Estonia, Portugal, Hungary, Poland, Ukraine, Romania, Bulgaria, Czech Republic, Slovakia, Belarus, Moldova, Republic Of, Sweden, Greece, Belgium, Italy, Ireland, Switzerland, Netherlands, Finland, Malta, Denmark, Lithuania, Croatia, Spain, Austria, Bosnia And Herzegovina, Iceland, Luxembourg, Macedonia, The Former Yugoslav Republic Of, Montenegro, Norway, Serbia, Slovenia, Albania, Cyprus, Latvia, Monaco, South Africa, Egypt, Algeria, Angola, Benin, Botswana, Burkina Faso, Burundi, Cameroon, Cape Verde, Central African Republic, Chad, Congo, Côte D'ivoire, Congo, The Democratic Republic Of The, Equatorial Guinea, Eritrea, Ethiopia, Gabon, Gambia, Ghana, Guinea, Guinea-bissau, Kenya, Lesotho, Liberia, Libyan Arab Jamahiriya, Madagascar, Malawi, Mali, Mauritania, Mauritius, Mayotte, Morocco, Mozambique, Namibia, Niger, Nigeria, Réunion, Rwanda, Senegal, Seychelles, Sierra Leone, Somalia, Sudan, Swaziland, Tanzania, United Republic Of, Togo, Tunisia, Uganda, Zambia, Zimbabwe, Georgia, Turkey, Israel, United Arab Emirates, Armenia, Azerbaijan, Bahrain, Iraq, Jordan, Kuwait, Lebanon, Oman, Qatar, Saudi Arabia, Palestinian Territory, Occupied, Yemen, India, Japan, Philippines, Pakistan, Thailand, Singapore, Viet Nam, Taiwan, Province Of China, Indonesia, Cambodia, Lao People's Democratic Republic, Malaysia, Myanmar, Korea, Republic Of, China, Afghanistan, Bangladesh, Bhutan, Kazakhstan, Kyrgyzstan, Maldives, Mongolia, Nepal, Sri Lanka, Tajikistan, Turkmenistan, Uzbekistan, Australia, Papua New Guinea, Kiribati, Palau, French Polynesia, Tuvalu, New Zealand

Posted

12 days ago

Salary

Not specified

No structured requirement data.

Job Description

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more.

Role Description

The Senior Director, Clinical Development, will provide medical and scientific leadership for oncology clinical trials across pre-clinical through phase 1-4 development. This role requires strong expertise in oncology, radiopharmaceuticals, and clinical drug development to ensure patient safety, scientific rigor, and regulatory compliance across assigned programs.

  • Serve as a medical leader within cross-functional development teams
  • Contribute to clinical strategy, protocol development, and regulatory interactions
  • Play a critical role in advancing clinical programs toward regulatory approval
  • Support future commercialization while partnering closely with Clinical Operations, Regulatory Affairs, Safety, Translational and other teams as needed

Qualifications

  • Medical Doctor (MD) degree from an accredited medical school required; Board certification in oncology strongly preferred
  • 5+ years of relevant industry experience, or an equivalent combination of industry experience, clinical practice, academic research, and demonstrated leadership in drug development
  • Demonstrated experience contributing to clinical development programs across one or more phases (Phase I–IV), preferably in oncology and/or radiopharmaceuticals
  • Proven ability to operate with increasing independence and accountability within cross-functional drug development teams
  • Experience participating in global regulatory interactions and contributing to clinical regulatory submissions

Requirements

  • Strong working knowledge of Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and global regulatory standards
  • Ability to apply clinical judgment and scientific rigor to complex development challenges
  • Excellent collaboration and communication skills, with the ability to engage effectively with both internal and external stakeholders
  • Strong analytical and problem-solving capabilities with a data-driven mindset
  • Proven ability to manage multiple complex programs and drive execution in a fast-paced, dynamic environment
  • Willingness to travel up to 30% of the time, including domestic and international travel as needed

Company Description

Job Requirements

  • Medical Doctor (MD) degree from an accredited medical school required; Board certification in oncology strongly preferred
  • 5+ years of relevant industry experience, or an equivalent combination of industry experience, clinical practice, academic research, and demonstrated leadership in drug development
  • Demonstrated experience contributing to clinical development programs across one or more phases (Phase I–IV), preferably in oncology and/or radiopharmaceuticals
  • Proven ability to operate with increasing independence and accountability within cross-functional drug development teams
  • Experience participating in global regulatory interactions and contributing to clinical regulatory submissions
  • Strong working knowledge of Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and global regulatory standards
  • Ability to apply clinical judgment and scientific rigor to complex development challenges
  • Excellent collaboration and communication skills, with the ability to engage effectively with both internal and external stakeholders
  • Strong analytical and problem-solving capabilities with a data-driven mindset
  • Proven ability to manage multiple complex programs and drive execution in a fast-paced, dynamic environment
  • Willingness to travel up to 30% of the time, including domestic and international travel as needed

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