Global Clinical Research Associate Professional
4 days ago
About the Role
We are seeking a skilled Global Clinical Research Associate to join our team. In this role, you will drive study performance at sites, perform site monitoring and onsite visit activities in compliance with procedural documents.
Key Responsibilities
- Contribute to the selection of potential sites and investigators, train and support them in study-related matters.
- Obtain and maintain essential documentation in compliance with ICH-GCP, Procedural Documents and local regulations.
- Perform source data verification according to SDV plan, ensure data query resolution and work with data management to ensure quality of the study data.
- Ensure accurate and timely reporting of Serious Adverse Events.
- Share relevant information on patient recruitment and study site progress within the local Study Team.
- Prepare for activities associated with audits and regulatory inspections in liaison with the local Study Team Lead and QA.
Additional Tasks
- Study-level tasks associated with Country Study Manager (CSM), act as a mentor for junior team members, co-monitor less-experienced CRAs within the study team.
- Contribute to process improvements, knowledge transfer and best practice sharing.
Requirements
- A strong working knowledge of Parexel processes, ICH-GCPs and other applicable requirements.
- Excellent communication and problem-solving skills.
- The ability to work independently and as part of a team.
- A high level of attention to detail and organizational skills.
Compensation and Benefits
We offer a competitive salary range of $80,000 - $110,000 per annum, depending on experience, as well as a comprehensive benefits package including health insurance, retirement savings plan and paid time off.
About Us
Parexel is a leading global biopharmaceutical services company that provides clinical research, medical communications, contract sales and market access expertise to pharmaceutical, biotechnology and medical device companies.
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