Senior Clinical Research Associate
hace 3 semanas
Job Summary
As a Clinical Research Associate, you will be responsible for coordinating all aspects of clinical monitoring and site management in accordance with regulatory guidelines and standard operating procedures. This role requires strong problem-solving skills, as you will be working independently or as part of a team to ensure the successful conduct of clinical trials.
Key Responsibilities
- Monitor multiple clinical trial sites across different therapeutic areas
- Assist other CRAs with co-monitoring activities, both remote and on-site
- Utilize customer service skills to deliver value, build loyalty, and trust with investigators and study coordinators
- Collaborate with the team to develop commitment to study timelines and objectives
- Review source data to ensure patient safety and data integrity
- Escalate concerns or issues to other departments as appropriate
Requirements
- Bachelor's Degree (or equivalent) with 2-4 years of relevant healthcare experience in the pharma or clinical research industry
- Minimum 3 years of monitoring and site management experience
- Strong experience in phase 1 trials
- Scientific background
- Proficiency with medical terminology
- Working knowledge of Local Regulations
- Demonstrated working knowledge of ICH/GCP Guidelines
- Excellent record-keeping skills and attention to detail
- Experience conducting Site Selection, Initiation, Routine Monitoring, and Close Out Visits
- Fluent in English, both written and oral
- Strong technical skills with CTMS, eCRF, eTMF
About ICON
Our focus is to provide a comprehensive and competitive total reward package that comprises not only an excellent level of base pay but also a wide range of variable pay and recognition programs. In addition, our best-in-class employee benefits, supportive policies, and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now and into the future.
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