Executive Director, Clinical Development
- Regular/Permanent
- USA / Texas
- Remote Options
Welcome to Orano
Every day we work to produce efficient low-carbon energy, to fight global warming, to find solutions that save natural resources, and to contribute to progress in health.
Our strengths? Across the entire fuel cycle, we have extensive expertise in cutting-edge technologies, safe, high value-added products and services, and a strong capacity for innovation. All of these factors reflect the strong skills of our 17,000 employees, whom we are constantly striving to develop. With their different backgrounds and experience, they are proof of our openness to all talents. They share the same ambition: to give nuclear energy its full value.
Job description
The Executive Director, Clinical Development will be responsible for providing clinical and scientific input into the development strategy for the clinical portfolio. In addition, the Dir., Clinical Development will provide medical oversight for ongoing clinical trials, including study document development (protocols, IBs etc.), overseeing outsourced medical monitoring, participating in internal clinical data reviews and assessments for safety reports.
Job Duties:
1. Develop and support implementation of the clinical development strategy for the entire portfolio. In conjunction with program management, author clinical development plans.
2. Support interactions with health authorities by providing clinical and scientific expertise and input into drafting of various submissions (INDs, annual reports, NDAs, inquiry responses etc). Attend meetings with health authorities as needed.
3. Provide medical oversight of ongoing clinical trials:
a. Review, analyze and interpret safety information for clinical trials and provide recommendations based on emerging safety data where appropriate.
b. Compile, analyze and present safety data analysis at (internal and/or external) safety review committee meetings.
c. Maintain oversight of outsourced medical monitoring activities for quality and study plan and SOP compliance.
d. Serve as medical resource for internal and external study teams to address medical / protocol related questions.
e. Regularly attend study team meetings.
f. Work with clinical team to ensure data collected are of high quality, including contributing to development of CRFs, edit checks and data review plans and regularly performs medical data review (including coding reviews).
4. May complete medical review including causality assessments for individual case safety reports and other safety/medical related regulatory documents.
5. Lead development of scientific publications, clinical trial design and protocols, investigator brochures and other study and/or asset level documents.
Represent the company at scientific meetings, conferences and interactions with Key Opinion Leaders, Investigators, health authorities.
6. Represent the company at scientific meetings, conferences and interactions with Key Opinion Leaders, Investigators, health authorities.
Our Full-Time Benefits
- Competitive compensation
- Health, Dental, and Vision insurance – with generous employer contributions
- 401(k) with employer matching and contribution amounts
- Life insurance and Short- and Long-Term Disability insurance provided by the company
- Generous Paid Time Off and holiday schedules
- Numerous Training and Development opportunities
- and more…
Ideal qualifications
All candidates must meet the following minimum requirements in order to be considered for this opportunity.
1. In-depth knowledge and prior experience in designing and implementing clinical development plans for pharmaceutical/biotechnology products. Prior experience with radioligand therapy development considered a plus.
2. Strong understanding of regulatory requirements for clinical development and ability to navigate interactions with health authorities.
3. Working knowledge of biostatistics and GCP / regulatory requirements and medical monitoring / medical data review practices.
4. Excellent verbal and written communication skills, including the ability to articulate complex scientific concepts to both technical and non-technical stakeholders. Fluency in written and spoken English
5. Licensed MD required.
Orano Med
Find out more about Orano Med