⏳ Last Date to Apply: Continuous Recruitment
Parexel Site Contracts Associate I or II Recruitment 2026: Apply Online
Site Contracts Associate I or II
Job Overview
Are you ready to step into a role where legal precision meets real-world impact? As a Site Contract Associate at Parexel, you will 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. Every clinical trial depends on clear, compliant, and timely agreements. As an SCA, you will help ensure research teams can focus on what matters most: bringing new treatments to patients who need them.
This is an entry-level opportunity with immense room for professional growth. You will become the go-to expert for site agreements, ensuring every contract supports the success of clinical trials across your region. You will work within a highly collaborative, virtual, and global team environment, learning from seasoned industry leaders and developing specialized skills in clinical trial operations and legal compliance.
- Drafting & Negotiating Contracts: Work on clinical study agreements, service agreements, team member agreements, and related documents.
- Compliance Management: Ensure all contracts adhere to ICH-GCP guidelines, local laws, and internal corporate policies.
- Stakeholder Communication: Act as the central communication hub between internal clinical teams, site staff, and external partners.
- Lifecycle Management: Oversee the full contract lifecycle from initial drafting to final signature and archival.
Key Job Details
| Company Name | Parexel |
| Job Role | Site Contracts Associate I or II |
| Experience | No prior industry experience required (Entry-level) |
| Salary Range | Competitive Industry Standard |
| Job Type | Private |
| Work Mode | Remote |
| Openings | Not Mentioned |
| Job Location | Romania (Remote) |
Key Responsibilities
- 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.
Requirements & Qualifications
- 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.
- Fluency in English (additional languages are a plus).
- Solid proficiency in MS Office (Word, Excel, PowerPoint).
Required Skills
- 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.
About Parexel
Parexel is a leading global clinical research organization (CRO) focused on providing comprehensive drug development and clinical trial management services. With a patient-centric approach, Parexel collaborates with pharmaceutical and biotechnology companies worldwide to accelerate the development of innovative, life-saving treatments. The company fosters an inclusive, collaborative, and growth-oriented work culture, empowering employees to make a meaningful impact on global health.
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