Investigator Contracts Lead - Manager (m/f/d)

JR Germany; Dresden; Remote; EUR 60.000 - 90.000; Vollzeit

Zusammenfassung

A leading company is seeking an Investigator Contracts Lead to manage site-facing contract negotiations and oversee the budget execution for clinical studies. This role requires extensive experience in clinical operations, strong negotiation skills, and the ability to work collaboratively across functions. The successful candidate will navigate complex contractual frameworks and build relationships with key stakeholders to ensure alignment and timely execution.

Qualifikationen

• 5+ years in clinical development operations or trial outsourcing.
• Experience with clinical study budgets and contracting negotiations.
• Knowledge of business, compliance, finance, legal, and drug development principles.

Aufgaben

• Responsible for direct site-facing contract and budget negotiations.
• Oversee contract execution with clinical investigator sites.
• Lead study-level site contracting activities.

Kenntnisse

Communication

Negotiation

Leadership

Risk Mitigation

Ausbildung

Bachelor's degree

Jobbeschreibung

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Investigator Contracts Lead - Manager (m/f/d), Dresden

Location: Dresden

Job Category: Other

EU work permit required: Yes

Job Views:

2

Posted:

29.06.2025

Expiry Date:

13.08.2025

Job Description:

The Investigator Contracts Lead is responsible for direct site-facing contract and budget negotiations, overseeing contract execution with clinical investigator sites, including initial agreements and amendments. This role involves managing the Per-Subject Cost (PSC) process, handling escalation and resolution of budget and non-legal issues, and collaborating to plan site contracting timelines during start-up.

• Balance risks for Pfizer in budget and contractual decisions while considering trial timelines.
• Develop, negotiate, track, and execute global clinical study agreements following GPD processes.
• Oversee the global site budget process.
• Negotiate costs and contractual terms directly with investigators and institutions, within approved templates.
• Build relationships with key investigative sites and Site Management Organizations.
• Lead study-level site contracting activities and serve as the primary contact for site issues.
• Partner with Legal and other divisions to manage escalations and improvements in site contracting.
• Coordinate with invoicing teams to ensure alignment with contracting and compensation requirements.

Basic Qualifications:

• 5+ years in clinical development operations or trial outsourcing, with a bachelor's degree.
• Experience with clinical study budgets and contracting negotiations.
• Knowledge of business, compliance, finance, legal, and drug development principles.
• Strong communication and presentation skills.
• Ability to mitigate risks to site contracting timelines.
• Leadership by influence in a matrix organization.

Preferred Qualifications:

• 2+ years in clinical operations with a US Juris Doctorate or similar legal degree.
• Experience drafting and negotiating Clinical Trial Agreements globally.

Work Location: Remote

Our Values:

Courage, Excellence, Equity & Joy

We foster a culture of innovation, responsibility, diversity, and joy, supporting our employees' growth and well-being through various initiatives and benefits.