Clinical Research Associate II (Respiratory)
New
R
Rho IncClinical Research
United StatesFull-TimeMiddle
Salary90,000 - 115,000 USD per year
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Job Details
- Experience
- Approximately 2 years+
- Required Skills
- MS Office
Requirements
- BA/BS, preferably in a life science, nursing, pharmacy or related field
- Approximately 2 years+ of on-site monitoring experience within the CRO, pharmaceutical, or biotechnology industry
- Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
- Computer literacy, including proficiency in MS Office
- Experience with EDC systems
- Strong written, verbal and presentation skills
- Attention to detail and strong organization skills
Responsibilities
- Perform all site monitoring visit activities, inclusive of all study visit types (PSV, SIV, IMV and COV)
- Participate in the site selection process with oversight from the Clinical Team Lead role
- Provide feedback to assist sites with resolution of detected deficiencies and corrective action needed, follow-up with sites until deficiencies are resolved
- Contribute to the development and review of protocols, study tools, and materials as well as documentation for clinical trials
- Provide mentoring, training, and co-monitoring of junior clinical team members
- Develop and maintain effective working relationships with clinical sites and within Rho as well as ensure communication of project goals and critical requirements
- Attend and present at meetings and conferences, including Investigator Meetings
- Participate in the RFP process, including business development meetings
- Participate in the Clinical Operations community at Rho by contributing to internal initiatives and standard operating procedures for the administration and monitoring of clinical trials
- Perform both onsite & remote monitoring and study closure activities across multiple protocols
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