183 Solar is a leading EPC (Engineering, Procurement, and Construction) firm specializing in solar energy solutions. With a focus on quality, innovation, and customer satisfaction, we aim to empower our clients to embrace renewable energy and reduce their environmental impact. Our team of experts is dedicated to delivering reliable, efficient, and sustainable solar construction services that meet the unique needs of each customer.

Thatch is an all-in-one platform that makes it easy to offer your employees the most personalized healthcare experience. You decide what to spend, and your team gets great health benefits. I started with the company in its early days as a Medical Advisor. I provided significant insight into scientific development, subject matter expertise, product development, mentoring, networking, forming strategic alliances, sales, and fundraising.

1. Clinical experience treating a variety of cancers including breast cancer, prostate cancer, CNS malignancies, lung cancer, head and neck cancers, gastrointestinal malignancies, lymphoma, leukemia, gynecological malignancies, and skin cancers2. Experience in the design, execution, and interpretation of Early Stage, Phase I, Phase II, and Phase III Clinical trials in Oncology therapeutic area 3. Experiencing leading clinical trials as Principal Investigator (PI) and Sub-Investigator (Sub-I) in multiple industry sponsored and institutional trials4. Leading the development of clinical protocols, protocol amendments, study reports, investigator’s brochure, safety sections, informed consents, statistical plans, and other clinical study-related documents5. Experience reviewing informed consent with patients and treating patients on oncology clinical trials and studies sponsored by pharmaceutical companies and national collaborative groups such as RTOG, NRG, SWOG, and NSABP6. Designing and executing clinical trial with responsibility of routine safety monitoring and pharmacovigilance including reporting any Adverse Events (AE’s) or Serious Adverse Events (SAE’s) to appropriate personnel, IRB, and FDA7. Experience working with institutional review board, and collaborating with study development teams, safety management teams, safety review board, contract research organizations (CROs)8. Knowledge of pharmaceutical dictionaries and understanding of MedDRA and WHO coding. Experience working with drug safety databases including ARGUS Safety database9. Knowledge and experience using statistical programs including SPSS and R10. Key contributor in writing and editing manuscripts for scientific publications, abstracts, posters, slide decks and presentations for scientific meetings including ASTRO, ASCO, and ESTRO11. Managing team members including clinical trials staff, nurses, therapy staff, medical assistants, medical writers, and physician residents

Acquired - OriginQS (https://www.originqs.com/)Navigate Oncology's proprietary software helps clinics manage cancer patients with smart oncology workflow solutions so patients receive treatment faster and smarter. Our software fully integrates with clinic's EMR/EHR to provide an end-to-end workflow solution for radiation oncology clinics in order to improve efficiency, reduce medical errors, minimize costs, and improve the prior-authorization experience.• Presented the business plan and pitch decks to venture capital, private equity, debt financing, private investors, and federal and state governments.• Raised $1.5M in funding.• Led successful global commercial product and service launch resulting in product’s early adoption at major medical centers• Developed relationships with KOLs to familiarize them with the product and drive early adoption

1. Medical Advisor to this startup company.2. Provided insight into scientific development, subject matter expertise, product development, mentoring, networking, forming strategic alliances, sales, and fundraising.

1. Clinical experience treating a variety of cancers including breast cancer, prostate cancer, CNS malignancies, lung cancer, head and neck cancers, gastrointestinal malignancies, lymphoma, leukemia, gynecological malignancies, and skin cancers2. Experience in the design, execution, and interpretation of Early Stage, Phase I, Phase II, and Phase III Clinical trials in Oncology therapeutic area 3. Experiencing leading clinical trials as Principal Investigator (PI) and Sub-Investigator (Sub-I) in multiple industry sponsored and institutional trials4. Leading the development of clinical protocols, protocol amendments, study reports, investigator’s brochure, safety sections, informed consents, statistical plans, and other clinical study-related documents5. Experience reviewing informed consent with patients and treating patients on oncology clinical trials and studies sponsored by pharmaceutical companies and national collaborative groups such as RTOG, NRG, SWOG, and NSABP6. Designing and executing clinical trial with responsibility of routine safety monitoring and pharmacovigilance including reporting any Adverse Events (AE’s) or Serious Adverse Events (SAE’s) to appropriate personnel, IRB, and FDA7. Experience working with institutional review board, and collaborating with study development teams, safety management teams, safety review board, contract research organizations (CROs)8. Knowledge of pharmaceutical dictionaries and understanding of MedDRA and WHO coding. Experience working with drug safety databases including ARGUS Safety database9. Knowledge and experience using statistical programs including SPSS and R10. Key contributor in writing and editing manuscripts for scientific publications, abstracts, posters, slide decks and presentations for scientific meetings including ASTRO, ASCO, and ESTRO11. Managing team members including clinical trials staff, nurses, therapy staff, medical assistants, medical writers, and physician residents

Startup experienceFundraisingVenture Capital

Internal Medicine