Site Contract Specialist-II/Contract Manager II; Sponsor Dedicated/Remote – Mexico, Argentina, Brazil) Syneos Health
Remote / Online - Candidates ideally in
San Mateo, San Mateo County, California, 94409, USA
Listing for:
Iax GmbH
Full Time, Remote/Work from Home
position
Listed on 2026-09-29
Job specializations:
-
Management
Regulatory Compliance Specialist, Contracts Manager
Salary/Wage Range or Industry Benchmark: 90000 - 130000 USD Yearly
USD
90000.00
130000.00
YEAR
Job Description & How to Apply Below
Site Contract Specialist-II / Contract Manager II (Sponsor Dedicated/ Remote – Mexico, Argentina, Brazil)
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
Required Qualifications:Bachelor’s degree in Business, Public Health, Life Sciences, or a related field (or equivalent experience).Demonstrated experience independently managing:Clinical Trial Agreements (CTAs)CTA AmendmentsSite budget negotiationsContract lifecycle management with minimal oversightStrong understanding of:CTA drafting and negotiationContract templates and fallback languageBudget development and negotiation strategiesClinical trial start-up processesExperience maintaining negotiation status and documentation within Sponsor clinical trial tracking systems.Excellent understanding of Phase II-IV clinical trials, ICH-GCP, and clinical development processes.Strong project management, organization, and prioritization skills.Exceptional negotiation, communication, and relationship-building abilities.Proficiency with Microsoft Office Suite.Preferred Qualifications:Previous experience supporting a Sponsor-Dedicated/FSP model.Leadership or mentoring experience (Senior level).CRO experience.Experience supporting process improvement initiatives within Site Start-Up or Site Contracts.Experience-Leveling:
SCS-I/Contract Manager 1:
Up to two (2) years of clinical research, site contracts and budgets, or related experience required.
SCS-II/Contract Manager 2:
Minimum of one (1) year of direct site contract and budget negotiations within CRO, site or pharma company required.
Sr. SCS/Contract Manager 3:
Minimum of two (2) years of direct site contract and budget negotiation required. Demonstrates strong skillset in overall contract and budget management/oversight and has a minimum of one (1) year of progressive experience leading site contract negotiations as client-facing point of contact within an industry sponsored clinical trial setting.
General Responsibilities:Review contract language and budgets for completeness and accuracy, and ensure that corrections are appropriately made and…
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