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Clinical Research Coordinator | Clinical Coordinator, Clinical Research Coordinator, Research Asso1

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Clinical Research Coordinator

Location:
Dulles, VA
Description:

Job Description | Clinical Research Coordinator Title | Clinical Research CoordinatorLocation | OpenDepartment | Clinical OperationsReports To | Director of Clinical Operations Overview The Clinical Research Coordinator (CRC) is responsible for activities associated with planning, initiating, coordinating, and implementing clinical trials within the SOFIE FAPI program under the direction of the Director of Clinical Operations. The CRC will maintain the Electronic Data Capture (EDC) system and serve as a liaison between SOFIE, clinical trial sites, and vendors. The CRC will also manage and support sites to reconcile study queries, address site issues, and generate reports as needed.Essential Duties and Responsibilities Provides study management, support, and coordination for FDA-regulated clinical research trials under the supervision of the Director of Clinical Operations. Perform data management activities on the EDC system and generate reports as necessary. Serve as a liaison with vendors, including tissue analysis support, image analysis, data management and laboratory services, and clinical personnel as necessary. Responds to correspondence, queries, and informational requests in a timely manner. Demonstrates compliance with Good Clinical Practice (GCP), Study Protocol, and any applicable healthcare and research regulations. Support sites with patient recruitment, enrollment, scheduling, and consent efforts. Ensure timely response to adverse events and any deviations per SOFIE guidelines. Responsible for completion of necessary documents for IRB or FDA in a timely manner. Work closely with the Regulatory lead to ensure appropriate data and documents are in place in support of regulatory filings. Perform additional duties and responsibilities as requested by Director of Clinical Operations or Chief Scientific Officer. The candidate is expected to travel 10% of time. Qualifications and Requirements Bachelor's degree or Master's degree in Sciences or related field. Minimum 2 years' experience as Clinical Research Coordinator or relevant research experience. Certified Clinical Research Coordinator (SOCRA or ACRP) preferred Attention to detail and strong organization capabilities. Strong interpersonal communication skills. Ability to take feedback constructively and function in a team-oriented work environment. Knowledge of Good Clinical Practices and FDA regulatory guidelines regarding clinical research. Project management and coordination skills. Proficient in MS Office applications required. Ability to work independently with minimal supervision in a remote setting.PDN-9b72623f-101b-4b85-acb3-a1bcab13e9f2
Company:
Monster
Industry:
Other
Posted:
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More About this Listing: Clinical Research Coordinator
Clinical Research Coordinator is a Nurse & Healthcare Clinical Coordinator, Clinical Research Coordinator, Research Associate Job at Monster located in Dulles VA. Find other listings like Clinical Research Coordinator by searching Oodle for Nurse & Healthcare Clinical Coordinator, Clinical Research Coordinator, Research Associate Jobs.