Study Start-Up Associate
Il y a 7 jours
Mechelen, remote, Belgique
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Temps plein
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JOB DESCRIPTION
You Will Fill Your Day With The Following Tasks
Benefits Of Working In ICON
Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with 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.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
Apply here: https://bit.ly/3x3mXZp
You Will Fill Your Day With The Following Tasks
- Assist in identifying study sites by performing site feasibility and recruitment tasks
- Complete essential document collection and review
- Organizes and maintain site clinical trial master file (TMF) documents
- Set up and maintain site-related data in applicable clinical systems
- Acts as primary site contact/liaison for study and site management issues
- Essential document collection, review, negotiation, to ensure successful site activation
- Recruitment of study sites
- Complete submissions and notifications to regulatory authorities, ethics committee and other bodies.
- Set up and maintain study documentation in applicable systems, e.g., clinical trial management system (CTMS), TMF system, applicable site/sponsor system
- Develop and grow with the advantages a big CRO can offer you
- Teams are organised in smaller organisations, so that you can still feel the team-spirit
- Interesting and competitive salary packages
- Training and Development programs
Benefits Of Working In ICON
Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with 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.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
Apply here: https://bit.ly/3x3mXZp