Clinical Research Sub-Investigator

We are seeking a Physician who is interested in learning the Clinical Research industry. This position will start as a Sub-Investigator but will blossom eventually into a Clinical Research Principal Investigator. This role will be in the Andersonville area with a fast-growing clinical research organization

Must be a certified MD or DO in the state of IL. Must be Billingual Spanish.

HIGHLIGHTSGreat opportunity to get into clinical research for the first time or continue a career with an organization 100% focused on bettering the clinical trial processMore consistent and stable work schedule and environmentLaid back environment compared to the hustle and bustle of a typical hospital setting

DAY TO DAYThis role will provide you oversight responsibilities over many different trials covering a variety of disease states, including cutting-edge research trials. These responsibilities include the execution of the clinical study protocol, the delegation of responsibilities to other site operations staff, ensuring compliance standards are met, and general oversight of the progress of studies.

Responsibilities:Carries out clinical evaluation and assessment of participants to ensure eligible participants are recruited and monitored for safety and adherence.Attends Site Initiation Visits (SIV), Pre-Selections Visits (PSV), and Investigators meetings as required.Participates in recruitment initiatives and strategy development to ensure targets are achieved; ensuring recruiting studies enroll according to plan within timelines and targets.Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants.Interprets protocols and IB.Manages and reviews IVRS, CRF/EDC, if applicable.Oversees management of investigational medical products (IMP).Identifies and reports trends within studies to manage them in light of conduct and outcome.Oversees multiple studies and/or studies with higher numbers.Cares for and protects the safety of participants through ethical conduct, this should receive the highest priority at all times during all aspects of the studyFulfills and complies with all medical duties, ensuring that clinical trials are performed to acceptable medical, scientific, and ethical standards and meet the requirements as per protocol, SOP/COP ICH, and local GCP guidelines and regulations.