File Clerk Salary at Nighthawk Enterprises Inc BETA

Position Overview: We are seeking a motivated and detail-oriented individual to join our team as a Clinical Research Coordinator. This is an excellent opportunity for someone looking to build a career in clinical research. No prior experience is required, but we are looking for candidates with a proven track record of longevity in their previous roles, demonstrating commitment and reliability. Key Responsibilities: Assist with the coordination and management of clinical trials in compliance with regulatory requirements and study protocols. Communicate effectively with study participants, physicians, and research team members. Schedule and conduct study visits, including data collection, sample handling, and documentation. Maintain accurate and organized study records, including electronic data entry. Support study start-up activities, such as preparing regulatory submissions and creating study binders. Ensure adherence to Good Clinical Practice (GCP) guidelines and institutional polici

Job Description Job Description Process and file documents and paperwork Scan files, emails, attachments and upload digital copies to the database Maintain and organize both the digital and hardcopy filing systems Retrieve documents, files, and paperwork when requested Deliver requested files to staff members Make necessary updates to records with new information; remove or archive any records that are outdated or obsolete Support functions as necessary Company Description Marko & Magolnick, P.A. is a multi-disciplinary legal practice concentrating on complex business transactions and litigation in South Florida and around the world. The firm’s attorneys have more than 60 years of combined experience in the law, business and non-profit sectors and are uniquely able to serve the needs of all clients, ranging from multinational corporations, to new business ventures to individuals. Company Description Marko & Magolnick, P.A. is a multi-disciplinary legal practice concentrating on complex

Role: Clinical Research Coordinator Location: Onsite - Miami, FL 33176 Relocation candidates will NOT be considered for this position Therapeutic Area: Asthma Employment Type: Position is a contract, project based support role - current contract duration is estimated to be 2-4 months, possibility for extension Schedule/ Shift: 30 hours a week, M-F Site is open as early as 7:30 AM for scheduling, but ideal work schedule would be 9-3pm M-F with some flexibility that if there is a need for them to come in earlier to help with patient screening etc or to handle calls. Responsibilities/ Job Duties: This candidate will work closely with all research staff to collect, store and maintain data in accordance with FDA Regulations, International Council of Harmonization and Good Clinical Practices. Responsibilities - May be the sole coordinator or work in collaboration with a research nurse on studies, responsible for source documents, data collection, data entry, query resolution, triggering fina

Job Description Job Description 25 HOURS FOR FILING CLERK, SPEAK CREOLE HAITIAN Company Description This Office is a small boutique law firm specializes in immigration law. Very fast paced. Company Description This Office is a small boutique law firm specializes in immigration law. Very fast paced.

Job Description Job Description Clinical Research Site seeking full time clinical research coordinator with experience. Must be Bilingual. Responsibilities: Must be able to manage an coordinate accordingly Must provide clinical research support to investigators to prepare for and execute assigned research studies including, reviewing protocols, case report forms, study specific documents and electronic data capture systems use to record research data Recruit and screen subjects for clinical trials and maintain all logs Orient research subjects to the study Design and maintain source documentation based on protocol requirements Schedule and Execute study visits and perform all study procedures Collect, Record and maintain research subject study data according to protocol and SOPS Handle lab testing and analysis including preparation of specimen collection tubes and lab logistic Monitor subject safety and report adverse reaction to appropriate medical personnel Trouble shoot study relate

Job Description Job Description Columbus Clinical Services is looking for experienced Clinical Research Coordinators (CRC) for their fast-paced, high-energy, clinical research site. Availability morning, evenings and weekends. CRCs may work up to 40 hours a week Proficient with phlebotomy and infusions. Create source documents for protocols using eCRF guidelines. Tracks medical or lab reports and report to physician for review and signature. Knowledge of medical terminology. GCP and IATA certification. Ability to function independently without close supervision Ability to multi-task and perform multiple critical tasks simultaneously Salary Range: Commensurate with Experience

Job Description Job Description Clerical Trial Assistant File Clerk / Office Services to assist at Trial Temporary - Jan 28 - Feb 24 We are working with a firm that needs a runner / assistant in a temporary capacity from January 28 - February 24 in Miami, FL. to assist attorneys and paralegals at a Trial. This is a unique opportunity for the right person. Qualified candidates MUST: - clean driving record and driver's license (over the age of 23) - be willing to sign a nondisclosure agreement - be able to commit for the duration - be organized, responsible, and punctual - be able to lift heavy boxes (multiple 50 lb boxes and/or equipment) - be available for overtime/weekends/evenings and to stay on-site at a hotel in Miami (room/board is paid). Job Duties: - prepare trial room with files - run file boxes to and from courthouse - stock and organize supplies - coffee, pens, lunch and dinner - run various errands for trial team (dry cleaner, grocery store, etc.) - be available for on-call

Senior Clinical Research Coordinator Job Post Are you a detail-oriented Clinical Research professional looking for a rewarding opportunity? Do you have at least 3 years of experience working in Clinical Trials involving human subjects? Are you willing to work a hybrid schedule out of our Fort Lauderdale, FL office? Are you looking for a company with an excellent benefits package, competitive salary, and company culture that is service-oriented? If so, we have the perfect position for you! Life Extension is a vitamin and supplement company that is looking for a Senior Clinical Research Coordinator. Please see full job description below, and information to apply! General Description: Coordinates, and supports the daily clinical trial activities and plays a critical role in the conduct of studies including the recruitment of study subjects. Collaborates with the Clinical Investigators and Clinical Research team to assist in the implementation of the research protocols as well as provide a