Clinical Research Associate II / Sr. CRA
R
RhoClinical Research
United StatesFull-TimeSenior
Salary90,000 - 140,000 USD per year
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Job Details
- Experience
- Approximately 2 years (CRA II) or 4-5 years+ (Senior CRA) of on-site monitoring experience
- Required Skills
- MS Office
Requirements
- BA/BS, preferably in a life science, nursing, pharmacy or related field.
- Approximately 2 years (CRA II) or 4-5 years+ (Senior CRA) 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.
- Proficiency in the use of EDC systems.
- Strong written, verbal and presentation communication skills.
- Strong organization skills for effective management of multiple sites and protocols.
- Ability to conduct 8-10 site visit days per month (up to 80% travel).
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.
- Contribute to the development and review of protocols, study tools, and materials for clinical trials.
- Provide mentoring, training, and co-monitoring of junior clinical team members.
- Develop and maintain effective working relationships with clinical sites.
- Attend and present at meetings and conferences, including Investigator Meetings.
- Participate in the RFP process, including business development meetings.
- Perform both onsite & remote monitoring and study closure activities across multiple protocols.
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