Start-up Team Lead

GENERAL - Lead start-up team during study start-up phase liaising directly with Lead SUPM or Project Lead, core team members and the client, as applicable. - Serve as client’s contact for start-up and maintenance processes and oversight. Responsible for establishing a strong working relationship with client’s project teams. - Monitor and control start up...

**Main activities**- With support from a more experienced start up team member, works on low complexity studies (e.g., internal CRU or smaller external site studies in the EU and US, generally not Sponsor facing).- Primary contact and liaison with investigative sites during study maintenance and, when assigned, site start-up (SSU) activities.- Ensures all...

The Clinical Team Lead (CTL) is the leader for the clinical team in our Clinical Operations **CTL** group. The Clinical Team Lead (CTL) is responsible and accountable for the execution of the clinical operations component of the project, at the global or regional level, as assigned. The CTL is responsible for working cross functionally, within a matrix...

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Clinical Team Lead RoleThe Clinical Team Lead is responsible for leading the clinical team in executing the clinical operations component of a project. This includes managing the team with emphasis on teamwork, quality, timelines, and metrics.

Owns all aspects of the appropriate proposal process (text, quote, budget, and/or response to Requests for Information [RFIs]) for assigned/accountable opportunities (inclusive of managing opportunities autonomously, establishing clear timelines, meeting client requirement, and resolving obstacles with mínimal support) - Responsible for managing...

**Regulatory Compliance Manager Role**\Main responsibilities of this key position include overseeing the readiness for audits and inspections from both clients and regulatory authorities, as well as actively participating in these events. In addition to ensuring compliance with all relevant regulations and guidelines, this individual will be responsible for...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or from a clinical trial. This includes, but is not limited to: - entry of safety data onto adverse event database(s) and tracking systems - review of adverse events for completeness, accuracy and appropriateness for expedited reporting - write...

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