Contract Specialist

Medpace; São Paulo; Presencial; BRL 60.000 - 100.000; Tempo integral

Resumo da oferta

An established industry player is seeking a Contract Specialist to join their dynamic team in São Paulo. This exciting role will involve preparing and negotiating vital agreements, managing site contracts, and ensuring smooth project execution. You'll be at the forefront of clinical trial management, collaborating with diverse teams to overcome challenges and meet project goals. With a focus on professional growth and a supportive work environment, this position offers a unique opportunity to make a significant impact in the clinical research field. If you're ready to leverage your expertise in a meaningful way, this could be the perfect fit for you.

Serviços

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Qualificações

• Bachelor's degree in business, legal studies, or life sciences required.
• CRO or investigator site experience preferred.

Responsabilidades

• Prepare, negotiate, and finalize Confidentiality Agreements and Clinical Trial Agreements.
• Manage contractual agreements with investigator sites and ensure compliance.

Conhecimentos

Negotiation Skills

Project Management

Communication Skills

Time Management

Problem-Solving

Formação académica

Bachelor’s degree in business administration

Bachelor’s degree in legal studies

Bachelor’s degree in life sciences

Descrição da oferta de emprego

Job Summary

Join Medpace at our Sao Paulo office! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Contract Specialist to join our LatAm Site Contract Team within the Clinical Operations team. This position will report to the LatAm Senior Contract Manager and will play a key role in the study start-up and clinical trial management processes at Medpace. The Contract Specialist will play a key role in advancing the start-up of our projects. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

1. Is responsible for preparing, negotiating, tracking and finalizing the Confidentiality Agreements (CDA), Clinical Trial Agreements (CTA), Budgets and Letters of Indemnification (LOI) as well as Amendments to these documents, as needed.
2. Manages all required contractual agreements with investigator sites, including distribution, negotiation of budget and language, tracking and finalization.
3. Proactively identifies site contract related risks and potential roadblocks.
4. Prepares contract approval timelines with investigators and leads efforts to obtain contract approval to meet study deliverables.
5. Maintains communication with project team and sites regarding status of all contractual requirements.
6. Collaborates with the project team to ensure the client deliverables and expectations are achieved.
7. Liaises with internal customers to review contract or budget areas that impact final execution of site contracts.
8. Maintains tracking regarding site contracts and provides regular updates as agreed by the study team to the project team and client regarding status and efforts to ensure timelines are maintained.

Qualifications

1. Bachelor’s degree in business administration, legal studies, or life sciences.
2. Ability to work with internal and external customers/vendors to meet project-specific goals.
3. Ability to manage high volume work and meet rigorous deadlines.
4. Flexibility to strategically manage negotiations with minimal oversight.
5. Ability to interact with site and other functional areas as secondary project contact for contracting issues and questions.
6. Ability to manage time and project requirements based on study deliverables.
7. CRO experience or investigator site experience negotiating site agreements preferred.
8. Fluency in English. Portuguese desirable.

***We kindly ask to send applications in English & salary expectation in BRL***

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

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