Clinical Research Associate II
Precision For Medicine
full-time
Posted on:
Location Type: Remote
Location: United Kingdom
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About the role
- You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
- You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
Requirements
- 4-year college degree or equivalent experience
- Candidates should ideally have more than 1 years CRA experience within the CRO or pharmaceutical industry.
- Oncology experience, early phase experience desirable although not essential.
- Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions)
- Fluency in English
Benefits
- CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life.
- You will have a lower than average number of protocols, setting you up to be a protocol expert.
- Travel is reasonable and your work/life balance will benefit as a result.
- Most meaningfully - your voice will be heard.
- Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical study monitoringregulatory submissionsprotocol adherenceSOPsICH-GCPdata recordingdata reportinginvestigator identificationpre-study visitsinitiation visits
Soft skills
organizational skillscommunication skillsinterpersonal skillsleadership skillsproblem-solving skills