Clinical Research Associate
New
W
WEP ClinicalClinical Research
Remote, USFull-TimeMiddle
Salary not disclosed
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Job Details
- Experience
- 1+ years
- Required Skills
- MS Office
Requirements
- Approximately 1+ years of on-site and remote clinical monitoring experience.
- BA/BS degree, preferably in life science, nursing, pharmacy, or a related field.
- Clinical background is preferred.
- Broad range of therapeutic experience.
- Proficiency with MS Office and EDC systems.
- High organizational and logistics skills to manage multiple sites and protocols.
- Superior written and verbal communication skills.
- Ability and willingness to travel up to 80%.
Responsibilities
- Schedule and perform on-site or remote monitoring visits including SIV, IMV/RMV, and COV.
- Review and verify patient records, informed consent, case report forms, and source documents for accuracy and compliance.
- Manage query resolution and assist sites with the resolution of detected deficiencies.
- Develop protocols, study tools, monitoring plans, and document templates.
- Document and report site protocol deviations and violations.
- Review investigational drug accountability and safety event documentation.
- Provide mentoring, training, and co-monitoring to junior team members.
- Assist in the development of standard operating procedures.
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