Investigator Contracts Lead - Spain - FSP

Parexel; Madrid; A distancia; EUR 50.000 - 90.000; Jornada completa

Descripción de la vacante

An innovative firm is seeking an Investigator Contracts Lead to join their remote team in Spain. This role is pivotal in negotiating clinical trial agreements, managing budgets, and ensuring timely site contracting. With a focus on patient wellbeing, you will collaborate with various teams to balance risks and timelines while leading site-facing activities. The position offers a unique opportunity to contribute to meaningful work in the healthcare sector, emphasizing professional growth and work-life balance. If you are passionate about making a difference and have a strong background in clinical operations, this could be the perfect fit for you.

Formación

• 5+ years of experience in clinical study budgets and contracting negotiations.
• Strong knowledge of business, compliance, finance, and drug development.

Responsabilidades

• Negotiate and execute global clinical study agreements with investigators.
• Oversee global site budget process and manage site contracting timelines.

Conocimientos

Clinical Trial Agreements

Budget Negotiations

Communication Skills

Risk Mitigation

Leadership by Influence

Educación

Bachelor’s Degree in Clinical Development

Juris Doctorate

Descripción del empleo

Investigator Contracts Lead - Spain - FSP

Parexel Madrid, Community of Madrid, Spain

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Investigator Contracts Lead - Spain - FSP

Parexel Madrid, Community of Madrid, Spain

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At Parexel FSP, people make a difference. We have a key mission: to prevent and treat disease by bringing important new medicines and therapies to patients in need. We achieve this through the expertise, experience, innovation, and commitment of our employees worldwide.

Our employees have the opportunity to do meaningful work globally while being supported locally in environments of challenge, collaboration, flexibility, and industry-leading growth potential.

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

This role involves direct site-facing contract and budget negotiations, managing the Per-Subject Cost (PSC) process, and collaborating with other teams to plan site contracting timelines.

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

We look for professionals committed to putting patient wellbeing first — for us, this is a job with heart.

Some Details Of The Role

• Balance risks to the sponsor with clinical trial timelines when making budget and contractual decisions.
• Develop, negotiate, track, and execute global clinical study agreements with investigators and institutions.
• Oversee the global site budget process.
• Negotiate cost, business, and contractual terms directly with clinical trial sites, within approved templates.
• Lead site contracting activities and serve as the primary contact for site contracting issues and timelines.
• Partner with Legal and other divisions to manage escalations and improve processes.
• Develop relationships with investigational sites and Site Management Organizations.
• Coordinate with invoicing teams to ensure alignment with site contracting and compensation.
• Interact with legal, study management, finance, and CRO teams.
• Contribute to major business initiatives or projects as needed.

Experience Required For This Role

• At least 5 years of experience with clinical study budgets and contracting negotiations.
• Experience in drafting and negotiating Clinical Trial Agreements in a global setting is preferred.
• Strong business, compliance, finance, legal, and drug development knowledge.
• Excellent communication and presentation skills.
• Ability to mitigate risks to site contracting timelines.
• Leadership by influence in a matrix organization.
• Fluency in written and spoken English.

Education

• Bachelor’s Degree or equivalent plus 5+ years in clinical development operations or outsourcing, OR Juris Doctorate plus 2+ years in the same fields.