Senior Clinical Research Associate, CNS/Oncology
Worldwide Clinical Trials
contract
Posted on:
Location Type: Remote
Location: United Kingdom
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Job Level
About the role
- Conduct all types of visits – site qualifications, initiation, interim monitoring, site management and study close-out visits
- Review study subject safety information and informed consent and conduct source document verification for compliance, patient safety, and veracity of data
- Actively participate in study team and investigator meetings
- Compile and ensure completeness of regulatory documents and ethical submission documentation and review study subject safety information and informed consent and study material (e.g. CRFs, manuals)
Requirements
- At least two years of independent clinical monitoring experience
- Demonstrable experience in handling multiple protocols across a range of therapeutic indications
- Four-year college curriculum in life sciences, OR Two-year college curriculum or equivalent education/training (nursing degree or equivalent life science degree)
- Ability to meet the travel requirements of the job
Benefits
- Extensive support through regulatory submissions
- TMF management with in-house CRAs
- Career path leading to Clinical Trial Manager roles
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical monitoringsource document verificationregulatory document compilationethical submission documentationstudy protocol managementpatient safety assessmentdata veracity verification
Soft Skills
team collaborationcommunicationorganizational skillsattention to detail
Certifications
nursing degreelife science degree