
Knowledgeable Clinical Research Coordinator and office manager adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues. Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities. Certified in Medical and Clinical trial Research. Detail-oriented team player with strong organizational skills. Ability to handle multiple projects simultaneously with a high degree of accuracy. Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals. Hardworking and passionate job seeker with strong organizational skills eager to secure entry-level Project Management or Lead Coordinator position. Ready to help team achieve company goals. To seek and maintain full-time position that offers professional challenges utilizing interpersonal skills, excellent time management and problem-solving skills. Well-qualified Medical Administrative professional successful at helping patients navigate medical office procedures while maintaining smooth and efficient business operations. Offering 10 years of related experience, diligent nature and expertise in electronic records management. Astute professional highly skilled in scheduling, training and managing busy Medical practices. Talented individual with 6 years of experience in payroll administration and new employee mentoring. History of positive management resulting in improved operations and employee retention. Proactive Clinical Coordinator excited to transition into a new position where superb leadership and clinical coordination abilities can be utilized. Skilled in task delegation, staff recruitment and scheduling. Committed to ensuring staff is compliant with all safety and health standards and protocols.
Senior lead Clinical Research Coordinator. Jobs include study start up, all regulatory, making sure all documents are signed and sent back to the sponsor, investigator meetings, training staff on protocol any all of their trainings required by sponsor, making source documents, making sure all IP has been received and accounted for, all labs are accounted for, keeping up with temperature of all devises used for lab storage and IP, communication between the site and sponsor, recruting,screening patients, completing study visit, lab draws and all other logistics of successful study execution of trials.