The Clinical Contracts Specialist (CC Specialist) is responsible for the timely development of country budgets and Clinical Trial Agreement templates during the start-up stage of a Clinical Trial. The CC Specialist will work closely with Project Management, Regulatory & Start-Up, Clinical Operations, Finance, Legal teams, and the client to ensure finalization of approved site budgets and execution of approved site Clinical Trial Agreements.
The adecuado candidate will be professional, analytical and possess excellent written and verbal communication skills.
Minimum Qualifications & Experience:
- Bachelor's Degree in a relevant field (science, law or other).
- Minimum 3 years' experience in the clinical trials industry including experience in contract and budget negotiation in multiple countries.
- Good knowledge of legal and medical terminology.
- Understanding of business/financial concepts used in clinical trials.
- Excellent communication and interpersonal skills. Good organizational skills; positive team player; attention to detail.
- Proven ability to collaborate effectively with internal stakeholders (Clinical operations, legal, finance, procurement) and external stakeholders (Clients and Sites).
- High level of attention to detail with the ability to manage multiple contracts and competing deadlines in a fast-paced environment.
- Experience in managing Business acumen
- Proficiency in Microsoft Office (especially in Excel)
- Ability to work collaboratively or individually in a fast-paced and deadline-driven environment.
Responsibilities:
Contracts
- Understand which Clinical Trial Agreement template is used by countries in Novotech geographies; and where site specific templates are applicable.
- Independent review and amendment of Clinical Trial Agreements within agreed negotiation parameters and policies.
- Escalate Clinical Trial Agreements outside of agreed negotiation parameters and policies as required; and obtain guidanc
📌 Clinical Contract Specialist – Europe Novotech (Madrid)
🏢 Iax
📍 Madrid
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