Senior Director - Nuclear Medicine Physician/Radiologist

Southern Arizona Legal Aid Inc.; United States; Remote; USD 150,000 - 250,000; Full time

Job summary

A leading medical organization is seeking a Development CRP to engage in clinical trials and imaging analysis. The ideal candidate will hold an MD or DO with significant experience in radiology or related fields, aiming to drive clinical strategies forward. Responsibilities include collaboration with research staff, analysis of clinical data, and ensuring compliance during studies. A strong foundation in drug development and excellent communication skills are essential.

Qualifications

• Advanced degree required (MD/DO) with 3+ years’ experience.
• Demonstrated knowledge of drug development process.
• Fluency in English with strong written and verbal communications.

Responsibilities

• Collaborate with clinical research staff on clinical trials.
• Analyze clinical findings to support safety and efficacy decisions.
• Provide expert interpretation of scans from clinical trials.

Skills

Interpersonal skills

Organizational skills

Negotiation skills

Teamwork

Communication

Education

MD/DO

Job description

The primary responsibilities of the Development CRP are generally related to compounds that are in development and include the following:

Collaborate with clinical research staff in the design, conduct and reporting of clinical trials
Analyze and summarize the clinical findings from studies to support decisions regarding safety and efficacy as well as regulatory strategy, results summarization and publications
Provide expert interpretation of scans obtained in clinical trials
Collaborate with Imaging Research and Development by providing imaging analysis expertise and making appropriate recommendations
Contribute to business unit and global alignment of clinical strategy and clinical plans
Understand and keep updated with relevant pre-clinical and clinical data
Anticipate the evolution of imaging and imaging applications and seek ways to position Lilly to best evaluate the potential value of these directions
Assist in developing, reviewing, and approving Phase 1-3 and post-market clinical imaging studies
Interface with scientific and educational organizations involved in clinical imaging
Support review of data analysis and the development of slide decks and publications (abstracts, posters, manuscripts)
Seek out opportunities to stay abreast of new developments in diagnostic imaging technology
Serve as resource to clinical operations personnel/ clinical research monitors, investigators and ethical review boards to address any questions or clarify issues arising during the conduct of study
Understand and actively address the scientific information needs of all investigators and personnel
Monitor patient safety during the conduct of studies and conduct the appropriate tracking and follow-up of adverse events, in alignment with corporate patient safety policies and procedures
Other duties as assigned

Minimum Qualification Requirements:

Advanced degree required (MD/DO) with 3+ years’ experience post training in appropriate specialty/subspecialty or have completed the comparable level of post-medical school clinical training relevant to the country of hiring. US trained physicians must have achieved board eligibility or certification
Non-US trained physicians must have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education (LCME).

Additional Preferences:

Medical residency/fellowship in Radiology, nuclear medicine or oncology preferred
Demonstrated knowledge of drug development process
Fluent in English; strong written and verbal communications
Demonstrated strong communication, interpersonal, organizational, teamwork and negotiation skills
Demonstrated ability to influence others (both cross-functionally and within the function) to create a positive working environment
Domestic and international travel estimated at 30%
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.