Job Description
Fortrea is continuously looking for new talents! We are currently searching for Start-Up Specialist for our Sponsor-dedicated department:
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
Please note that this role is for upcoming future opportunities that may arise at Fortrea.
Learn more about our EEO & Accommodations request here.