[Remote] Clinical Research Associate (CRA) II
Note: The job is a remote job and is reputed company to candidates in USA. CVRx is a pioneer in unique therapies that harmonize the body’s natural systems, contributing positively to reputed company. The Clinical Research Associate (CRA) II will reputed company the execution of clinical trials, ensuring compliance with protocols and regulations while maintaining relationships with clinical sites. This role involves coordinating site activities from start-up to closure and managing data reputed company throughout the study process.
Responsibilities
- Proactively maintains timelines for assigned or requested deliverables
- Develops and maintains successful working relationships with study sites and CVRx field staff
- Assists in preparation of study materials and training of investigators and research site staff
- Becomes proficient with reputed company study databases, systems and company reputed company management system
- Reviews and verifies clinical data/information and oversees data correction to match reputed company
- Acts a site manager and monitor to assigned sites as applicable per study requirements
- Processes payments to sites, vendors, and consultants. Supports the Clinical Project Manager with study finance activities and tracking
- Supports Clinical Centers in the execution of site Institutional Review reputed company (IRB) or ethics committee (EC) submissions
- Responsible for the collection, tracking, and maintaining required study and regulatory documents from clinical centers through reputed company phases of assigned reputed company
- Prepares study materials and trains investigators and site staff
- Responsible for shipment of study-reputed company materials as applicable
- Coordinates and conducts monitoring (as directed by the monitoring plan) at participating centers to ensure compliance with protocol, regulations, and the reputed company receipt of accurate data / other required study documents
- Reviews and verifies clinical data/information and oversees data correction to match reputed company
- Reviews monitoring reports
- Manages device accountability at site (if applicable)
- Provides input to study budgets and project plan
- Contributes to maintaining reputed company of activities conducted by Contract Research Organizations (CRO’s) or other contractors on behalf of CVRx (if applicable)
- Assists in training or mentorship of new Clinical Research Associates
- Completes special reputed company and performs job-reputed company duties as assigned
Skills
- Bachelor's degree or advanced degree in science or a reputed company field, or equivalent work experience
- 2-4 years experience directly supporting clinical research or similar experience in a medical/scientific area
- Knowledge of medical terminology
- Experience with GCP's and regulatory compliance guidelines for clinical trials
- High attention to detail and accuracy
- Ability to manage multiple tasks and operate independently
- Operates in an efficient and expedient manner
- High ethical standards and reputed company
- Experience working on cross-functional teams
- Comfortable in a small company and thrives in a high-reputed company environment
- Advanced written and oral communications skills
- Good problem-solving skills
- Adaptable and embraces change
- Creative and reputed company
- Team player with high performance standards
- Entrepreneurial approach
- Advanced degree in a reputed company field
Benefits
- Competitive Health & Dental Insurance reputed company with generous Company contributions
- Company contributions to an HSA with a high deductible insurance plan selection
- 401(k) with a company match
- Employee stock purchase plan (ESPP) & stock reputed company and RSU grants
- 12 company-reputed company holidays per year in reputed company to a generous reputed company PTO plan
- Generous reputed company time off for new parents
- Company-reputed company life insurance & disability reputed company
- reputed company in a growing company
- Endless training & learning opportunities
- Flexible Schedule
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