Site Contracts Lead - US/LATAM - Remote

Worldwide Clinical Trials; Durham (NC); Remote; USD 90,000 - 130,000; Full time

Job summary

A leading global CRO is seeking a Site Contracts Lead to oversee site contracting activities and mentor team members. This remote role requires strong negotiation skills and a deep understanding of clinical research regulations. Join us to enhance healthcare through innovative research practices.

Qualifications

• 6+ years of industry experience preferred.
• Experience in negotiating complex contracts within clinical research.
• Knowledge of international and local regulatory requirements (e.g., FDA, EMA, ICH-GCP).

Responsibilities

• Serve as the main contact for Study site contracting activities.
• Lead and provide subject matter expertise on Clinical Trial Agreement processes.
• Mentor and supervise Site Contracts Specialists.

Skills

Negotiation

Communication

Leadership

Education

Bachelor's degree in relevant fields

Tools

MS Office

Job description

Join to apply for the Site Contracts Lead - US/LATAM - Remote role at Worldwide Clinical Trials.

We are a global, midsize CRO dedicated to pioneering approaches in clinical research to find cures for persistent diseases. Our team of over 3,500 experts works passionately to improve lives, fostering a diverse and inclusive environment where everyone can thrive.

The Site Contract Department is responsible for reviewing, drafting, and negotiating clinical research site contracts, investigator contracts, and other project-related agreements, ensuring compliance with applicable laws and regulations worldwide.

Key Responsibilities

1. Serve as the main contact for Study site contracting activities with Project Teams and Sponsors.
2. Lead and provide subject matter expertise on Clinical Trial Agreement processes.
3. Present and communicate site contract negotiation strategies and updates during meetings.
4. Negotiate contract templates, language, and budget parameters with stakeholders.
5. Mentor and supervise Site Contracts Specialists to ensure effective execution.
6. Ensure timely delivery of contract updates and manage risk by developing contingency plans.
7. Collaborate with cross-functional teams to support study activation and compliance.

Qualifications

1. Experience in negotiating complex contracts within clinical research or related industries.
2. Excellent communication skills in English.
3. Knowledge of international and local regulatory requirements (e.g., FDA, EMA, ICH-GCP).
4. Leadership skills to guide junior team members.
5. Bachelor's degree in relevant fields; 6+ years of industry experience preferred.
6. Proficiency with MS Office tools.

Join us to make a difference in the world of healthcare. For more information, visit our careers page or connect with us on LinkedIn. We are committed to equal employment opportunities and fostering an inclusive environment.