Fortrea is growing! For one of our client we are currently looking for a Start-Up Specialist.
Responsibilities (but not only):
Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner.
May support the negotiation of site contracts and budgets with sites if applicable and track progress of contract and budget milestones/developments intervening and escalating as appropriate.
Collect and track all the necessary documents required and perform a quality review formatting and compilation of the final documents for effective and compliant site activation and maintenance without supervision.
Participate in team and project meetings as applicable.
Review and customize country and site-specific patient informed consent forms for compliance with local requirements and protocol. Proactively resolve informed consent issues and other potential difficulties with study sites.
Experience:
Minimum of 2 years of experience in clinical development o
Working knowledge of ICH RA IRB/IEC and other applicable regulations/guidelines; familiarity with investigator start-up documents and contract/budgets negotiation process
Learn more about our EEO & Accommodations request here.
Required Experience:
IC
Fortrea is growing! For one of our client we are currently looking for a Start-Up Specialist.Responsibilities (but not only):Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner.May support the negotiation of site contracts and budgets with ...
Fortrea is growing! For one of our client we are currently looking for a Start-Up Specialist.
Responsibilities (but not only):
Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner.
May support the negotiation of site contracts and budgets with sites if applicable and track progress of contract and budget milestones/developments intervening and escalating as appropriate.
Collect and track all the necessary documents required and perform a quality review formatting and compilation of the final documents for effective and compliant site activation and maintenance without supervision.
Participate in team and project meetings as applicable.
Review and customize country and site-specific patient informed consent forms for compliance with local requirements and protocol. Proactively resolve informed consent issues and other potential difficulties with study sites.
Experience:
Minimum of 2 years of experience in clinical development o
Working knowledge of ICH RA IRB/IEC and other applicable regulations/guidelines; familiarity with investigator start-up documents and contract/budgets negotiation process
Learn more about our EEO & Accommodations request here.
Required Experience:
IC
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