Join the HBA Team!
Join Our Team! At Healthcare Business Associates, we’re always on the lookout for talented and passionate individuals to join our dynamic team. If you’re ready to take your career to the next level and make a difference, we encourage you to explore our postings. Submit your resume below and become part of a supportive and innovative work environment where your contributions valued and recognized!
Our Staffing Opportunities
Principal Investigator (PI)
The Principal Investigator provides the essential leadership and scientific oversight required to ensure that every clinical trial is conducted with the highest level of integrity and participant safety. This individual is legally responsible for managing the research team and maintaining strict adherence to all regulatory standards and ethical protocols throughout the duration of the study.
Sub-Investigator (Sub-I)
The sub investigator provides vital clinical expertise by conducting participant assessments and performing protocol specific procedures to ensure the safety of every individual in the trial. This role supports the primary leadership in managing the daily execution of the study while maintaining complete and accurate documentation in accordance with all professional standards.
Medical Director
The medical director serves as the primary clinical authority for the organization by providing the high level strategic guidance and medical oversight necessary to ensure the integrity of all patient care activities. This individual is responsible for establishing clinical standards and maintaining a culture of safety and excellence that aligns with the professional mission and the operational goals of the practice.
Site Director / Site Manager
The research medical director provides the strategic leadership and clinical oversight necessary to ensure that all study protocols align with the scientific mission and the regulatory requirements of the organization. This individual serves as the primary clinical authority for the research portfolio and maintains the highest standards of participant safety and data integrity across every trial.
Clinical Research Coordinator (CRC)
The site director or research manager provides the high level operational leadership and administrative oversight necessary to ensure that clinical trial activities are executed efficiently and in full compliance with study protocols. This individual manages the daily clinic operations while coordinating with sponsors and stakeholders to maintain the financial health and organizational growth of the research site.
Research Nurse
The research nurse provides specialized nursing care and clinical oversight to study participants while ensuring their safety and well being throughout the trial process. This individual maintains the highest standards of protocol compliance and data collection to support the scientific goals and regulatory requirements of the organization.
Regulatory Coordinator / Quality Specialist
The regulatory coordinator and quality specialist manages the essential documentation and submissions required to maintain full compliance with institutional review boards and federal guidelines throughout the study lifecycle. This individual performs meticulous quality control audits and process reviews to ensure that every aspect of the research operation meets the highest standards of accuracy and data integrity.
Patient Recruitment Coordinator
The patient recruitment coordinator designs and implements strategic outreach initiatives to identify and engage qualified individuals for enrollment in clinical trials. This individual serves as the primary link between the community and the research site while ensuring that recruitment targets are met through effective communication and meticulous follow up.