What are the responsibilities and job description for the Principal Investigator (Physician) position at Pinnacle Clinical Research?
Come join our team and make a difference as we blaze the way into the future of medical discovery through world-class clinical research. At Pinnacle Clinical Research, we are committed to driving innovation and advancing medical knowledge. Through our rigorous research studies, we strive to unlock breakthroughs that have the potential to transform patient care and improve lives. We pride ourselves on conducting high-quality research as a complement to the medical care that our volunteers receive from their routine care center. Together, we will raise awareness about the importance of clinical research and its role in shaping the future of healthcare. Be a part of the discovery!
Summary : Responsible for administering activities to facilitate clinical research and providing clinical support for the conduct and oversight of all phases of clinical trials.
Duties and Responsibilities :
- Works with affiliate or collaborating research sites.
- 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.
- Maintains subject and document confidentiality at all times and understands and complies 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.
- Performs 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. Reviews and adjudicates all lab, imaging, and biopsy findings.
- Reviews and holds expert knowledge of study-related activities and protocols.
- Adheres to study protocols, Food and Drug Administration regulations, and good clinical practices at all times.
- Assists in the preparation for study monitor visits.
- Performs subject screening and recruitment.
- Provides some weekend coverage to facilitate study visits per protocol.
- Provides after-hours phone call coverage as needed.
- Oversee Sub-Investigators and recruitment team.
Education / Experience :
One to two years of research experience as a Principal Investigator for Phase I-IV clinical trials. Experience in GI and / or liver disease is preferred.
Certificates and Licenses :
Current physician license. Board Certified preferred.
Knowledge, Skills, and Other Abilities :
Work Environment and Physical Demands :
The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
Perks of working at Pinnacle Clinical Research :
Pinnacle Clinical Research is an equal-opportunity employer. All applicants will be considered for employment without regard to race, color, religion, disability, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status, or any other protected Federal, State / Province or Local status unrelated to the performance of the work involved.
About Pinnacle Clinical Research :
Pinnacle Clinical Research Network provides world-class clinical trial solutions to its member sites, sponsors, CROs, researchers and patients to accelerate the results of their trials. By advocating for quality, integrity and diversity in clinical research data, Pinnacle is dedicated to advancing unmet areas of medical research and leading pivotal scientific discoveries.
