Offre d'emploi n° 9660661

Start-Up Specialist France

Type de contrat : CDI
Localisation : Hauts-de-Seine - Rueil-Malmaison
Entreprise : Labcorp
Fonction : Commercial - Vente

Publiée le 22/04/2023
Expérience souhaitée : 1 à 2 ans
Niveau d'études souhaité : Bac / Bac Pro

Description du poste

As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.

Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical and regulatory expertise.

Did you know?

In July 2022, Labcorp announced its intention to spin off its clinical development business as a separate public company, subject to the satisfaction of certain customary conditions. Fortrea will become the new brand identity for our Clinical Development business in connection with the spin-off, which is expected in mid-2023.

We believe that the exceptional is possible when you have the right partner, so we are looking for the right people to help build a transformative force in Clinical Development. www. fortrea. com

What we have to offer: a strong international support network, flexible working solutions that facilitate a genuine work-life balance, a highly competitive compensation package and the opportunity to significantly raise your profile in the industry.

Your tasks

  • Prepare and performs Regulatory Submissions for France (EC, CA, CNOM, EU CTR Part II etc...) until authorization
  • Prepare and negotiate Site Agreements (Site contract and budget) until execution and track progress of milestones / developments, intervening and escalating as appropriate
  • Customize all country documents including Participant Information Sheet/ Informed Consent Form to ensure compliance with local requirements and protocol
  • Serve as the primary contact for investigative sites, proactively managing site activation and providing guidance for your sites during the start-up phase of your assigned studies
  • Ensure that all assigned maintenance and start-up activities are on track and in accordance with client expectations, ICH / GCP, SOPs, budget, quality and all applicable local laws and guidelines
  • Collect, track and perform a quality review of all essential and investigator documents required for effective and compliant study site activation and maintenance
  • Liaise with our regulatory department regarding document submission requirements and ensure documents required are collected and submitted on time. Ensure high quality documents are filed and systems are updated on an ongoing and timely basis, taking ownership for compliance and audit readiness
  • Escalate any issues with submissions and / or approvals for your assigned studies appropriately and in a timely fashion, both to internal departments and to external stakeholders such as Ethics Committees (ECs) and local regulatory authorities
  • Possible involvement in Site outreach/feasibility


  • Degree in a relevant field such as pharmacology, life sciences, clinical trial management, (veterinarian) medicine, health care (management), nursing, chemistry, biology, etc.,
  • In lieu of the above, an equivalent completed vocational education or equivalent professional experience


  • Solid expertise in clinical trials within a CRO or a pharmaceutical company with a specialization in clinical study start up / regulatory submissions
  • Demonstrated understanding of research protocol requirements as well as the ability to communicate them / educate others about them
  • Proven track record collaborating successfully with operational project teams as well as external investigative sites and local regulatory authorities (including ECs)
  • Familiarity with investigator start-up documents and contract / budget negotiation processes with study sites
  • Autonomous work style with excellent time and project management skills
  • Experience of feasibility or site identification activities would be beneficial but is not essential
  • Business fluency in French and English – both spoken and written

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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