Investigator Contracts Lead - Spain - Fsp

buscojobs España; Madrid; A distancia; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

A leading company in the pharmaceutical industry is seeking an Investigator Contracts Lead in Spain for a fully remote role. The position involves managing contract negotiations and overseeing budget processes for clinical trials. Ideal candidates will have strong negotiation skills, experience in clinical operations, and a commitment to patient wellbeing. Join a team that values flexibility and professional growth while making a meaningful impact in healthcare.

Formación

• At least 5 years in clinical study budgets and contracting negotiations.
• Experience drafting and negotiating Clinical Trial Agreements in a global setting preferred.

Responsabilidades

• Managing site-facing contract and budget negotiations.
• Overseeing contract execution with clinical investigator sites.
• Building relationships with investigational sites and organizations.

Conocimientos

Communication

Leadership

Negotiation

Educación

Bachelor’s Degree

Juris Doctorate

Descripción del empleo

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Investigator Contracts Lead - Spain - FSP, Alcobendas

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Client : Parexel

Location : Spain

Job Category : Other

EU work permit required :

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Job Views : Posted :

07.05.2025

Expiry Date : 21.06.2025

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Job Description :

When our values align, there's no limit to what we can achieve.

At Parexel FSP , people make a difference. We aim to prevent and treat disease by bringing new medicines and therapies to patients. Our employees leverage their expertise, experience, innovation, and commitment worldwide.

We offer meaningful work globally, supported locally in environments of challenge, collaboration, flexibility, and growth potential.

Parexel FSP seeks an Investigator Contracts Lead in Spain , 100% remote.

This role involves managing site-facing contract and budget negotiations, overseeing contract execution with clinical investigator sites, managing the Per-Subject Cost (PSC) process, and collaborating across departments to ensure timely site contracting.

Expect professional challenges balanced with a healthy work-life balance, emphasizing wellbeing and patient care.

We value professionals who prioritize patient wellbeing, viewing this role as a job with heart.

Role responsibilities include :

• Balancing risks and trial timelines in budget and contractual decisions.
• Developing, negotiating, and executing global study agreements.
• Overseeing the global site budget process.
• Negotiating terms with investigators / institutions, within approved templates.
• Leading study-level site contracting activities and acting as primary contact.
• Partnering with Legal and other divisions for escalation and process improvements.
• Building relationships with investigational sites and organizations.
• Collaborating on invoicing and payment processes.
• Interacting with various legal, clinical, and finance teams.
• Contributing to major initiatives and projects.

Required experience :

• At least 5 years in clinical study budgets and contracting negotiations.
• Experience drafting and negotiating Clinical Trial Agreements in a global setting preferred.
• Knowledge in business, compliance, finance, legal, and drug development.
• Strong communication and presentation skills.
• Leadership by influence in a matrix organization.
• Fluency in English.

Education :

• Bachelor’s Degree with 5+ years in clinical operations or outsourcing, OR Juris Doctorate with 2+ years in similar fields.

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