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Senders Pediatrics
Clinical Research Coordinator
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What they do
A Clinical Research Coordinator directs clinical research and development projects for companies, and coordinates testing and quality control.
$110,372 / year median in Ohio
+14% projected growth
Job Description
Clinical Research Coordinator Senders Pediatrics South Euclid, OH Job Details Full-time From $21 an hour 2 hours ago Benefits Health savings account Health insurance Dental insurance Paid time off Employee assistance program Vision insurance Employee discount Life insurance Retirement plan Qualifications Teamwork Bachelor's degree Attention to detail Organizational skills Productivity software Time management Database software proficiency Full Job Description Senders Research, the clinical research arm of Senders Pediatrics, has been conducting clinical trials in collaboration with pharmaceutical companies and academic institutions since 1995. We have developed a national reputation for our expertise in conducting both safety and immunogenicity trials involving vaccines, oral and topical antibiotics and antifungals and inhaled bronchodilators and corticosteroids. The Research Assistant/Coordinator will enjoy being a member of a dynamic and enthusiastic team of research professionals who oversee research services here at Senders Pediatrics. Some responsibilities of the Research Assistant/Coordinator include: To ensure the safe and ethical conduct of clinical research as well as compliance with the International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) regulatory requirements. To recruit subjects for clinical studies by making phone calls, sending mailings and discussing studies with parents and potential participants. To become proficient in study start up, ongoing study management including data capture and adverse event processing and study close out requirements. To become proficient in phlebotomy the accurate processing of blood, sera and other biological specimens and the administration of vaccines. To develop excellent time management, organization, planning and prioritization skills critical to the successful management of multiple clinical trials. To interact with research sponsors and their representatives in a positive, ethical and productive manner. To interface with the clinical staff, including front office, medical assistants and providers in promoting the activities of the research department. To be willing to participate in other research-related duties that may be assigned Knowledge, skills and experience required: Bachelor's Degree in the sciences or related area is required Minimum 1 year in Clinical Research, or recent college grad with biology major and strong interest in clinical research Phlebotomy skills and confidence in vaccine administration are preferred although we are willing to train Competence with computers, databases and the MS office suite Possesses a growth mindset Takes a team approach to work Willingness to be challenged and to gain mastery in new areas Maintains close attention to detail in all work related areas