Key Facts

Remote From:

Hungary , Romania , Czechia , Croatia , Serbia

Full time

Mid-level (2-5 years)

English, Czech

Hard Skills

Contract Management

Other Skills

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Negotiation
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Communication
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Analytical Thinking
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Problem Solving
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Microsoft Office
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Teamwork
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Detail Oriented
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Professionalism

Roles & Responsibilities

Bachelor’s degree in law, economics, business, social sciences, or a related field
Strong negotiation skills and diplomacy
Excellent written and verbal communication
Solid proficiency in MS Office (Word, Excel, PowerPoint)

Requirements:

Drafting and negotiating contracts — clinical study agreements, service agreements, team member agreements, and related documents
Ensuring compliance with ICH-GCP, local laws, and internal guidelines
Acting as the communication hub between internal teams, site staff, and external partners
Managing the full contract lifecycle — from first draft to final signature and archival

Parexel

Pharmaceuticals

About Parexel

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

Company type: XLarge

Industry: Pharmaceuticals

Founded: 2018

Company size: 10001

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Job description

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

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Are you ready to step into a role where legal precision meets real‑world impact? As a Site Contract Associate, you’ll be the driving force behind the agreements that make clinical trials possible. If you thrive on negotiation, communication, and keeping complex processes running smoothly, this is your chance to shine.

This is a homebased role but you must be living in one of the following countries:

Croatia
Czech Republic
Hungary
Romania
Serbia

What You’ll Do

You’ll become the go‑to expert for site agreements, ensuring every contract supports the success of clinical trials across your region. Your responsibilities will include:

Drafting & negotiating contracts — clinical study agreements, service agreements, team member agreements, and related documents.
Interpreting site feedback within local legal and business frameworks to guide internal decision‑makers.
Ensuring compliance with ICH‑GCP, local laws, and internal guidelines.
Acting as the communication hub between internal teams, site staff, and external partners.
Managing the full contract lifecycle — from first draft to final signature and archival.
Building strong relationships with clinical trial sites and internal stakeholders.
Spotting risks early and collaborating with the Site Contract Lead to resolve them.
Tracking progress in real time and keeping teams informed.
Driving process improvements to make contracting faster, clearer, and more efficient.

What You Bring

You’ll excel in this role if you have:

Strong negotiation skills and the diplomacy to navigate complex conversations.
Excellent written and verbal communication.
A talent for problem‑solving and analytical thinking.
The ability to work confidently in a virtual, global team.
Grace under pressure and a polished, professional presence.
A sharp eye for detail and a commitment to quality.
Fluency in English (additional languages are a plus).
Solid proficiency in MS Office (Word, Excel, PowerPoint).

Education & Experience

Bachelor’s degree in law, economics, business, social sciences, or a related field.
No prior industry experience required — this is an entry‑level opportunity with room to grow.

Why This Role Matters

Every clinical trial depends on clear, compliant, and timely agreements. As an SCA, you’ll help ensure research teams can focus on what matters most: bringing new treatments to patients who need them.

Ready to apply?

APPLY

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