Principal Investigator
Location: Houston, TX
This role is Full time Onsite
Are you a physician with experience as a PI on a clinical trial? Tired of the grind of seeing so many patients each day? Want to jump into Clinical research full time and never have to be on call again? Want your weekends off? This is for you!!
Some things you will do in this role include:
- The Principal Investigator is the primary individual responsible for the preparation, conduct, and administration of all designated projects in compliance with applicable laws and regulations and institutional policies
- Work with affiliate or collaborating research sites
- Assist in the preparation for study monitor visits
- Perform subject screening and recruitment
- Maintain subject and document confidentiality and understand and comply with the appropriate sponsor requirements, regulations including the Food and Drug Administration, Good Clinical Practice, International Conference on Harmonization, Health Insurance Portability and Accountability Act, Institutional Review Boards, and institutional policies and procedures
- Perform study related procedures such as physical examinations, informed consent, subject history, adverse events, test article handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessments. Review and adjudicate all lab, imaging, and biopsy findings
- Review and hold expert knowledge of study related activities and protocols
Some things you will bring to the role include:
- MD with current US medical license. Board Certification in internal medicine (or equivalent)
- 1 to 2 years of research experience as a principal investigator, GI and liver experience preferred
- Bilingual (Spanish) or the ability/desire to learn conversational Spanish needed
For immediate consideration, email emily@scientificsearch.com and mention Job#