EMEA Clinical Contracts Specialist

Advanced Clinical

Italia

In loco

EUR 42.000 - 66.000

Tempo pieno

2 giorni fa
Candidati tra i primi
Generatore di candidature

Una candidatura mirata per questo annuncio — un curriculum e una lettera di presentazione pensati per rispondere alle esigenze dell'annuncio.

Supera i filtri ATS

Descrizione del lavoro

Advanced Clinical in Italy is seeking a Clinical Contracts Associate to manage the preparation, negotiation and execution of clinical trial contracts and budgets across EMEA. You will work with research sites and collaborate with legal, compliance and clinical teams to resolve issues and keep studies moving forward.

The role requires at least four years in clinical research, hands-on contract experience, and strong written and spoken English.

Competenze

  • Minimum of four years in clinical research, pharmaceuticals, medical devices or a clinical environment.
  • Strong hands-on experience with clinical trial contracts and site budget negotiation.
  • Ability to work independently, manage deadlines and handle confidential information.
  • Excellent written and spoken English; able to negotiate directly with research sites.

Mansioni

  • Prepare, review and negotiate clinical site agreements, work orders, amendments and change orders.
  • Adapt study budget templates to country and site requirements, reflecting protocol activities and policies.
  • Assess contractual risk and propose practical solutions.
  • Negotiate terms covering indemnification, IP, confidentiality and compensation.
  • Review country and site changes to informed consent wording related to injury, data privacy and compensation.
  • Manage workload independently and mentor colleagues as needed.

Conoscenze

Contract negotiation
Clinical budgeting
Independent work
Communication

Formazione

Degree or equivalent experience

Strumenti

Microsoft Word
Microsoft Excel

Descrizione del lavoro

Advanced Clinical in Italy is seeking a Clinical Contracts Associate to manage the preparation, negotiation and execution of clinical trial contracts and budgets across EMEA. You will work with research sites and collaborate with legal, compliance and clinical teams to resolve issues and keep studies moving forward.

The role requires at least four years in clinical research, hands-on contract experience, and strong written and spoken English.

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