Sponsor Dedicated Study Start Up Lead with Finance expertise based in Munich

Reposted 18 Days Ago
Be an Early Applicant
Munich, Bayern
In-Office
Mid level
Biotech
The Role
Oversee clinical trial site activation, regulatory processes, and manage financial aspects including budget negotiations and contract oversight. Collaborate with stakeholders to ensure compliance and effective execution of protocols.
Summary Generated by Built In

We are looking for a sponsor-dedicated Country Start-Up Lead to oversee clinical trial site activation, regulatory processes, and financial management. This is a well suited role for someone with experience in clinical start-up operations, budget negotiations, and regulatory compliance and who enjoys working collaboratively to drive progress.

Key responsibilities:

  • Responsible for execution and oversight of clinical trial country submissions and approvals for assigned protocols.

  • Responsible for managing country deliverables, timelines, and results for assigned protocols to meet country commitments.

  • Work closely with internal and external stakeholders, including sponsors, CROs, and site teams, to streamline processes.

  • Negotiate investigator budgets, oversee financial forecasting, and manage trial-related expenses

  • Through continual interaction with local clinical team/s successfully delivers clinical and financial contracts within fair market value.

  • Oversight and tracking of clinical research-related payments.

  • Payment reconciliation at study close-out.

Qualifications:

  • University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology (Fortrea may consider relevant and equivalent experience in lieu of educational requirements).

  • Strong background in clinical research, including a few years in start-up, preferably in a lead position

  • Skilled knowledge of budget and contract negotiations, local regulatory environment and submission and approval processes

  • Fluent in German and in English, with effective communication and negotiation skills.

What we Offer:

  • An hybrid model allowing you to collaborate effectively with your teams (2 days at client's office in Munich and 3 days working from home).

  • Opportunities for professional development, mentorship, and career progression.

  • Work with an industry-leading sponsor and expand your leadership capabilities.

  • Thanks to our ERGs (Employee Resource Groups), join divers communities that foster inclusion, professional development, and networking.

  • Access to mental health support, wellness initiatives, and fitness programs.

If you are ready to make an impact, collaborate with top professionals, and bring your expertise to a meaningful role, we'd love to hear from you!

#LI-GQ1 #LI-Hybrid

Learn more about our EEO & Accommodations request here.

Top Skills

Budget Negotiations
Clinical Trial Site Activation
Financial Management
Regulatory Processes
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The Company
HQ: Research Triangle Park, NC
10,811 Employees

What We Do

Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network.

Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.

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