Job Title

We are hiring for a TEMPORARY/CONTRACT Sub Investigator, Clinical Research. This individual can be either an NP, PA, MD or DO. Must be licensed in the state of Ohio. This position is 100% onsite, full-time hours and 3 months in duration. Clinical Research experience is preferred, but not required. Summary The Sub Investigator (Sub-I) is responsible for patient safety, accurate data collection, and ensuring the well-being of clinical trial participants. This role provides clinical oversight and support to research coordinators, principal investigators, and study staff. Responsibilities Lead study teams in the execution of clinical trials Train and mentor staff on protocols, GCP/ICH guidelines, communication, and trial management Develop training plans, mitigation strategies, and quality control processes Conduct and manage trials in compliance with protocols, GCP, ICH guidelines, and company SOPs Oversee all trial activities, including startup, recruitment, scheduling, visits, vendor management, and closeout Ensure timely and accurate data entry, query resolution, and proper documentation practices Monitor, manage, and report adverse events, serious adverse events, and protocol deviations Implement protocol amendments and ensure team adherence Manage regulatory documentation and submissions to sponsors and IRBs Evaluate and pre-screen potential study participants Develop and execute recruitment strategies with recruitment teams Apply project management principles to mitigate risk and improve study quality Communicate effectively with internal teams, sponsors, CROs, vendors, and participants Ensure confidentiality of patient, sponsor, and company information Oversee staff delegation, training, and documentation Develop escalation pathways to maintain patient safety and protocol compliance Plan studies considering timelines, endpoints, vendors, and target populations Incorporate understanding of financial impact, product development lifecycle, and protocol design Perform clinical procedures within scope (e.g., drug administration, phlebotomy, ECGs, lab processing) Maintain knowledge of the disease or condition under study Promote cultural awareness and professionalism Perform additional duties as assigned Qualifications Required Skills/Abilities: Must be licensed as a MD, DO, NP, or PA in the state you work in. Must undertake all training and certification required by sponsors and CRO's to carry out clinical trials within specified timelines. Safe handling of data and records regarding privacy and confidentiality, per HIPAA requirements. Practices professionalism and integrity in all actions - Demonstrated ability to foster concepts of teamwork, cooperation, self- control, and flexibility to get the work done Ability to communicate effectively in English (both verbal and written). Up to 10% travel, as needed, for project team meetings, client presentations and other professional meetings/conferences as needed. * We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO), and the California Fair Chance Act (CFCA). * This position is subject to a background check based on its job duties, which may include patient care, working with vulnerable populations, access to financial and confidential information, driving, working with heavy machinery, or working in a warehouse or laboratory environment. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.