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| Company: | Massachusetts General Hospital |
| Industry: | Healthcare / Medical |
| Job Type: | Full Time |
| Country: | United States |
| State/Province: | Massachusetts |
| City: | Boston |
| Post Date: | 04/27/2024 11:11 AM |
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GENERAL SUMMARY/ OVERVIEW STATEMENT: The Massachusetts General Hospital Division of Cardiology is seeking a highly motivated and experienced individual for a Clinical Research Coordinator (CRC) I position to assist with ongoing and future clinical research studies. The CRC I must be able to multi-task in a dynamic clinical research setting. The ability to work well in a team is a must. This is the ideal position for someone looking to work with a dedicated group of people to make new and enhanced medical device technology available to patients with an array of cardiac conditions. The CRC I will gain invaluable experience in the field of Cardiology in an academic clinical research setting. This is a full-time (40 hours/week) position; evening and weekend hours may occasionally be required to facilitate the conduct of the study. This position is ideal for someone interested in pursuing graduate studies or a career in the fields of medicine, public health, or clinical research. It involves extensive patient interaction as a member of a clinical research team. PRINCIPAL DUTIES AND RESPONSIBILITIES : The Clinical Research Coordinator I has the following duties and responsibilities: 1. Manages investigational device trials under the supervision of the PI, including data entry and accuracy, Institutional Review Board maintenance, and extensive patient interaction with study participants. 2. Verifies accuracy of study forms 3. Updates study forms per protocol 4. Documents patient visits and procedures 5. Maintains research data, patient files, and study database 6. Acts as liaison between Sponsor and PI 7. Collects, organizes and manages study and patient data 8. Develops and implements recruitment strategies 9. Screens patients for enrollment into clinical trials and following research subjects per study protocol. 10. Verifies subject inclusion/exclusion criteria 11. Acts as study resource for patient and family 12. Submits all Institutional Review Board (IRB) documentation 13. Prepares documents and study binders for FDA audits (if needed) 14. Orients and trains junior team members on the study protocols as appropriate 15. Prepares invoices and directs, verifies, corrects patient care charges as appropriate 16. Uses software programs to generate graphs and reports 17. Obtains patient study data from medical records, physicians, etc. 18. Conducts library searches 19. Assists with regulatory binders and QA/QC procedures 20. Assists with interviewing study subjects 21. Administers and scores questionnaires 22. Provides basic explanation of study and in some cases obtains informed consent from subjects 23. Performs study procedures, which may include phlebotomy. 24. Assists with study regulatory submissions 25. Writes consent forms and obtains consent for applicable trials 26. Performs administrative support duties as required 27. Requests medical records from external institutions 28. Maintains a good understanding of the study protocols and study start-up process FISCAL RESPONSIBITY: May monitor and manage study funds. Responsible for preparing invoices and for directing, verifying, and correcting patient care charges as appropriate. SKILLS/ABILITIES/COMPETENCIES REQUIRED : • Careful attention to details • Good organizational skills • Ability to follow directions • Good communication skills • Computer literacy • Working knowledge of clinical research protocols • Ability to demonstrate respect and professionalism for subjects' rights and individual needs LICENSES, CERTIFICATIONS: Training in CITI and GCP preferred. EDUCATION:
EXPERIENCE:
Massachusetts General Hospital is an Equal Opportunity Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. Applications from protected veterans and individuals with disabilities are strongly encouraged. | |
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