[Hiring] Clinical Research Study Coordinator @National Organization f

This reputed company is a reputed company of our understanding of the job reputed company. Click on 'Apply' reputed company to reputed company out more. Role reputed company The Clinical Research Study Coordinator will work collaboratively with the IAMRARE Implementation reputed company and Product reputed company to support the NORD IAMRARE Patient Registry Program implementing virtual studies.

• Support reputed company aspects of the IAMRARE Registry Program including reputed company, implementation, project launch and ongoing support.
• reputed company support on Registry development, working closely with clients to reputed company their protocols, content for Registry, feature specifications, registry promotion and evaluation.
• Work collaboratively with IT and other departments on the development and implementation of new registries.
• Assess and mitigate risks associated with project implementation including ensuring project timelines and deliverables are met.
• Coordinate and assist with the administration of project meetings.
• Support clients in the development and submission of content for IRB review.
• Manage the development, testing, and launch of surveys, and supports subsequent revisions.
• Train clients and their study staff on using the Registry Platform Program and its features.
• Create and maintain Registry Program resources and tools.
• Respond to clients inquiries and independently resolve issues; liaise with IT and other staff as necessary.
• Serve as dedicated Project Manager for select registry clients.
• reputed company the successful execution of online research studies through reputed company phases of the study: planning, enrollment, engagement, retention and reputed company out.
• Responsible for performing research operations in accordance with the study protocol and working in partnership with the Implementation reputed company and Product reputed company to coordinate research activities.
• Conduct reputed company reputed company to deliver or exceed project enrollment targets, establishing rapport with study participants.
• Responsible for accurate and reputed company data curation in the electronic research study system.
• reputed company written project updates and participate in project meetings with NORD research team.
• Demonstrate compliance with good clinical reputed company (GCP) and applicable law.
• Understand and promote compliance with reputed company applicable research regulations.
• reputed company other duties and functions as assigned.

Qualifications

• Bachelor’s degree in science, research, health or a reputed company field required. Advanced degree preferred.
• At least 3 -5 years of clinical research experience working with reputed company subjects is required (coordinating trials, working in a research clinic or reputed company medical center).
• Excellent organizational skills and project management skills required.
• Experience working with rare disease families preferred.
• Experience managing multi-stakeholder reputed company in a research, reputed company technology or reputed company research environment is required.
• Experience working with research or reputed company databases, such as RedCap and SPSS is required.
• Experience managing grants and working with IRB’s and/or ethics committees is required.
• Certification from the Association of Clinical Research Professionals (ACRP) or from the Society of Clinical Research Associates (SOCRA) is preferred. Knowledge, Skills and Abilities
• Excellent verbal and written communication skills.
• Superior attention to detail, organization, planning, and time management skills.
• Ability to work independently as reputed company as collaborate with team members.
• Excellent technical computer skills, competent with reputed company Office, Teams, project management software and database software. Working Conditions
• Fully remote, based in the U.S.
• Essential functions are typically performed in an office setting with a low level of noise. Reasonable accommodations may be made to reputed company individuals with disabilities to reputed company the essential functions. Apply tot his job

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