Site Contracts Specialist I /Contract Manager I (Sponsor Dedicated/ Remote-Arge

🏢 Syneos Health India Private Limited · all Syneos Health India Private Limited jobs
📍 Brazil
📅 Posted 2026-08-12 · via Himalayas
🏷 Site-Contracts-Specialist,Contract-Management,Clinical-Trial-Contracts,Site-Start-Up,Clinical-Research,Site-Contract-Specialist,Site-Contracts-Associate,Clinical-Site-Contracts-Specialist,Site-Budget-And-Contract-Specialist
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Site Contracts Specialist I /Contract Manager I (Sponsor Dedicated/ Remote-Argentina, Brazil, or Mexico) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. • We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Job Responsibilities ite Contracts Specialist I /Contract Manager I – Sponsor Dedicated Remote Argentina, Brazil, Mexico Are you looking to grow your career in clinical research contracts and site start-up? We are seeking a Contract Manager I to join a high-performing Sponsor-Dedicated team supporting a leading global biopharmaceutical company. In this role, you will support the negotiation and management of clinical trial agreements, amendments, and study budgets while partnering with internal stakeholders and investigative sites to help advance clinical research. This is an excellent opportunity for an early-career contracts professional who is detail-oriented, collaborative, and eager to develop expertise in clinical trial contracting and budgeting. WHO YOU ARE Required Qualifications - Bachelor’s degree in Business, Public Health, Life Sciences, or a related field (or equivalent experience). - Up to two (2) years of experience in clinical research, site contracts and budgets, contract administration, or a related field. - Basic understanding of: - Clinical Trial Agreements (CTAs) - Site budgets and budget negotiations - Contract lifecycle management processes - Clinical trial start-up activities - Strong organizational skills with the ability to manage multiple priorities and deadlines. - Excellent verbal and written communication skills. - Strong attention to detail and problem-solving abilities. - Ability to work collaboratively in a fast-paced, team-oriented environment. - Proficiency in Microsoft Office Suite. Preferred Qualifications - Experience in a CRO, pharmaceutical, biotechnology, or clinical research environment. - Exposure to clinical trial agreements, research budgets, or study start-up activities. - Familiarity with clinical trial management systems (CTMS) or other contract tracking tools. - Knowledge of ICH-GCP and clinical research processes. WHAT YOU WILL DO - Manage the execution of Clinical Trial Agreement Amendments (CTA AMDs) and related contract documents using approved templates, fallback language, and Lead guidance. - Manage execution of Confidentiality Disclosure A

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