IHCRA
About the role
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In House Clinical Research Associate (IHCRA) | Taiwan
At ICON, it's our people that set us apart.
As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them?
To be a successful IHCRA, we will provide you adequate training and support enabling you to confidently perform the essential duties satisfactorily and your job responsibilities are not limited to the following:
Become familiar with ICON's SOPs/WPs, ICH GCP guidelines, regulations and systems.
Maintain timelines and ensure accuracy and completeness of data entered into ICON systems
Become familiar with the principles of and assist with investigator recruitment
Serve as the primary in-house contact for sites and investigators participating in studies
Conduct and complete remote site management activities, with support as needed, according to applicable SOPS and the Study Monitoring Plan.
To contact Clinical sites for specific requests (e.g. enrolment updates, missing documentation, data entry timeliness, data query follow-up, CDA finding follow-up, and action Item resolution or other sponsor specific CRA tasks.
Takes responsibility for project tasks and sees these tasks through to successful completion, with support.
Maintains a professional interpersonal relationship with study team, sites, and Sponsor.
Participates in QA Audits as needed.
Regularly attends and contributes to project specific and departmental meetings
Ability and willingness to travel as needed (drive and fly)
Maintains Sponsor and patient confidentiality
General ad hoc duties and administration as requested
What you need
Ability to liaise successfully and interact positively with clinical project teams, customers, site staff and all levels of staff across relevant departments.
Effective prioritization skills, ability to multi-task and meticulous attention to detail.
Comprehensive knowledge and understanding of ICH-GCP and other relevant regulations for the conduct of clinical trials related to pharmaceuticals, biologics, medical devices and combination products.
Competent computer skills
Good oral and written communication skills
Due to the nature of this position, it may be required for the employee to travel. Therefore dependent on the employee's location, a valid driver's license will be required
Foreign language skills desirable
Other duties as assigned
Global or local CRO work experience advantageous
Application process
Once you find a job opening that fits your skills and interests, you can create an account, apply and check back on the progress of your application or apply for other roles. Once your application has been received, a confirmation email will be sent to your email.
Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.
One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.
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