Principal Specialist, Site Contracts

Job not on LinkedIn

🔥 1 minute ago

🇩🇪 Germany – Remote

⏰ Full Time

🔴 Lead

✨ Contracts Specialist

👻 Ghost score 25%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Lifelancer

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2020

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Pre Seed Round on 2022-03

Consulting • Healthcare • Logistics

Lifelancer is an AI-powered talent hiring platform that connects employers with skilled professionals in the Life Sciences, Pharmaceutical, and IT sectors. It enables individuals to create profiles showcasing their skills, get matched with high-paying international jobs or projects, and facilitates hiring and payroll for employers in multiple countries. The platform aims to streamline the hiring process with efficient AI sourcing and compliance support.

📋 Description

• Act as a Subject Matter Expert on Clinical Trial Agreement processes at country and site level • Prepare, negotiate, and finalize site contracts and budgets • Manage the Investigator Budget • Act as a key liaison for contract-related communications • Resolve negotiation issues and escalate risks • Drive process improvements • Contribute to SOP development and keep templates updated • Liaise and collaborate with Worldwide stakeholders and external stakeholders, including sites and investigators • Review and finalize Clinical Trial Agreements and associated documents, including site budgets, for completeness and accuracy

🎯 Requirements

• Mastery in negotiating complex contract terms with clinical sites and vendors • In-depth understanding of international and local regulatory requirements for clinical trials, including FDA, EMA, and ICH-GCP • Ability to explain complex contract terms clearly and concisely • Leadership skills to guide and support junior contract specialists • Ability to collaborate effectively with legal, finance, data protection, and clinical operations teams • 3–4 years of experience as a Senior Site Contracts Specialist or minimum 5 years of Site Contract experience in the clinical research, pharmaceutical, or CRO industry • Bachelor's Degree or equivalent in business administration, finance, law, science, or a related field • Proficiency with MS Word, Excel, and Outlook • Knowledge and understanding of ICH and GCP Guidelines • Knowledge of local country legislation and regulatory requirements for clinical trials

🏖️ Benefits

• Diverse and inclusive work environment • Supportive and cohesive teams • Hands-on, accessible leaders • Equal employment opportunities • Employee experience focused on respect and inclusion