Start-Up Specialist - Sponsor dedicated

Posted 12 Days Ago
Be an Early Applicant
Paris, Île-de-France, FRA
In-Office
Junior
Biotech
The Role
The Start-Up Specialist I will manage submission processes, liaise with teams, track documents, and ensure smooth site activation for clinical studies.
Summary Generated by Built In

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.

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    The Company
    HQ: Research Triangle Park, NC
    10,811 Employees

    What We Do

    Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.

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