Job Title

Clinical Research CoordinatorClinical Research site seeking Full time Clinical Research coordinators .MINIMUM REQUIRED EDUCATION AND EXPERIENCEHigh school diploma (A BS would be a plus) or educational equivalent and relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training and experience Applicable certifications and licenses as required by the company, country, state, and/or other regular Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP).RESPONSIBILITIES* Be able to manage team and coordinate accordingly* Provide clinical research support to investigators to prepare for and execute assigned research studies, including:* Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data.* Attend all relevant study meetings;* Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research.* Recruit and screen patients for clinical trials and maintain subject screening logs* Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits.* Design and maintain source documentation based on protocol requirements* Schedule and execute study visits and perform study procedures* Collect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness* Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics* Monitor subject safety and report adverse reactions to appropriate medical personnel; Correspond with research subjects and troubleshoot study-related questions or issuesMINIMUM REQUIR ED EDUCATION AND EXPERIENCEHigh school diploma (A BS would be a plus) or educational equivalent and relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training and experience Applicable certifications and licenses as required by the company, country, state, and/or other regulatory bodiesJob Information* Responsibilities prior to study initiation. Attend IM, SIV and any other training session required by the sponsor.* Develop its own source documents and give them to QC Dept. for revision. Review that the Trust System is accurate when it comes to pt. compensation.* Perform a meeting with laboratory personnel and assistant coordinator(s) (if applicable) prior to initiation of the study to train them on the new protocol.* Make sure that all study supplies i.e. lab kits, study medication, diaries, questionnaires, scales, IRB approvals including but not limited to ICF are on site prior to initiation. Make sure that all personnel listed on the Delegation Log have completed all the training required by sponsor.Requirements* FMG, MA certificate or RN license, medical terminology* Strong computer skills, including Word, Excel* Work well in a team environment and excellent communication skills.* Certified Clinical Research Coordinator (Plus)* /*Excellent management experience* Excellent organization skills and initiative with the ability to drive processes under minimal supervision* Strong proficiency with Microsoft Office applications and statistical analyses software* Excellent written, oral communication skills and time management skills* Ability to travelMust be Bilingual (English and Spanish)#medicaldevice #hiring #robotics #medicalrobotics #engineering #clinicalresearch #engineeringcareers #maximumeffort #clinicalcoordinatorjob #clinicalcoordinatorresearchEmployment TypeFull-timeJob FunctionsCompensation based on experienceJob Type: Full-timePay: $15.00 - $35.00 per hourWork Location: In person