Clinical Project Engineer- Medical Device

Benefits: 401(k) 401(k) matching Relocation bonus Title: Clinical Project EngineerLocation: Lake Forest, CAJob Description & Skill Requirement:Key Responsibilities:Supporting to team to design, plan and develop clinical evaluation research bench studies.Supporting to conduct registered and non-registered non-clinical bench studies of products that havebeen determined to satisfy a medical need andor offer a commercial potential.Supporting to assist in interpretation of results of non-clinical investigations in preparation for new drug,device or consumer application.Supporting to team to resolve operational aspects of clinical trials in conjunction with project teams andin accordance with standard operating procedures (SOP), good clinical practice (GCP) and specificcountry regulations and prepare clinical trial budgets and responsible for clinical supply operations, siteand vendor selection1. Site Selection and Initiation:Assist in the selection of investigative sites for clinical trials.•Conduct site initiation visits to train and educate site staff on the study protocol, regulatoryrequirements, and proper handling and storage of ophthalmic drugs and medical devices.•Ensure recruitment strategies are in place to meet enrollment targets.2. Monitoring and Site Management:•Conduct on-site and remote monitoring visits according to the protocol monitoring plan to ensure dataquality and regulatory compliance.•Review source documents, case report forms, and patient records.•Verify the informed consent process and adherence to the study protocol.•Ensure that instrumentsequipment used in the clinical trials are correctly calibrated, maintained, andutilized according to the study protocol and regulatory standards.•Collaborate with Clinical Operations Lead and Clinical Trial Team to identify and resolve site quality orstudy execution issues.3. Regulatory Compliance:•Ensure that the clinical trial sites are compliant with applicable regulatory requirements (e.g., FDA,ICH, GCP) regarding ophthalmic drugs and medical devices.•Ensure that the Investigator Site File is maintained and audit ready.4. Investigational Product and Clinical Supplies Oversight:•Verify subject qualification and correct IP was dispensedimplanted.•Confirm full reconciliation of IP at the site level•Monitor device-related safety and performance concerns and report them to the study sponsor.•Ensure proper handling, storage, and accountability of investigational drugs andor medical devices.Ensures appropriate clinical supplies are available and adequate for clinical trial.5. Data Management:•Verify data accuracy and completeness, including instrumentdevice-generated data.•Collaborate with data management team to resolve data-related issues.6. Safety Reporting:•Ensures all safety issues are communicated and managed by Principal Investigator according toregulatory and protocol requirements.7. Close-Out Visits:•Conduct close-out visits to finalize data collection and ensure all study-related activities are completedin accordance with the study protocol and regulatory requirements.8. Documentation and Reporting:•Complete comprehensive and accurate monitoring reports, including site follow-up letters.•Ensure CTMS and eTMF are up to date and audit pensation: $90,000.00 - $100,000.00 per year MAKING THE INDUSTRY'S BEST MATCHESDBSI Services is widely recognized as one of the industry's fastest growing staffing agencies. Thanks to our longstanding experience in various industries, we have the capacity to build meaningful, long-lasting relationships with all our clients. Our success is a result of our commitment to the best people, the best solutions and the best results. Our Story:Founded in 1995Privately Owned CorporationManaging Partner Business ModelHeadquartered in New JerseyUS Based Engineers OnlyCollaborative Team ApproachMethodology and Process DrivenGET HIREDTop performing engineers are the foundation of our business. Our priority is building strongrelationships with each employment candidate we work with. You can trust our professionalrecruiters to invest the time required to fully understand your skills, explore your professionalgoals and help you find the right career opportunities.

Created: 2025-03-01