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Sr Site Contracts Specialist Assigned To Client In Brazil

0-2 years
Not Disclosed
10 Oct. 10, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Sr Site Contracts Specialist – Client Assignment in Brazil

Updated: Yesterday
Location: BRA-Client
Job ID: 25102364


Company Overview

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate clinical, medical affairs, and commercial insights into outcomes to address modern market realities.

Our Clinical Development model centers the customer and patient, while continuously streamlining processes to make Syneos Health easier to work with and a better place to work.

Join a team of passionate problem solvers collaborating to deliver therapies faster and improve lives.

WORK HERE MATTERS EVERYWHERE


Why Syneos Health

  • Career development and progression opportunities

  • Supportive and engaged line management

  • Technical and therapeutic area training

  • Peer recognition and total rewards program

  • Inclusive Total Self culture encouraging authenticity

  • Diversity of thoughts, backgrounds, and perspectives ensures everyone belongs


Job Responsibilities

Contract & Budget Management

  • Lead multi-country projects including negotiating and preparing contracts, budgets, and related documents for industry-sponsored clinical trials.

  • Produce site-specific contracts from country Clinical Trial Agreement (CTA) templates.

  • Review, own, and submit proposed CTAs and investigator budgets for site review.

  • Negotiate budgets and contracts with sites, Sponsor, and Site Contracts Service Centre until issues are resolved.

  • Perform quality control, arrange execution of CTAs, and archive documents with metadata.

Process & Compliance

  • Administer contract management processes for protocol, consent, institution, investigator, vendor, consultant, and customer agreements.

  • Generate amended contracts/budgets as necessary, streamline internal processes, and provide creative solutions.

  • Collaborate with legal, clinical operations, finance, and Site Contract Service Center to ensure alignment with sponsor agreements.

  • Identify operational risks and propose proactive solutions.

Communication & Leadership

  • Act as liaison between site contracts staff, internal teams, and external customers.

  • Provide functional guidance and keep stakeholders informed of contract statuses and pending issues.

  • Train and mentor junior staff on SOPs, ensuring high-quality deliverables.

  • Participate in discussions on company goals, departmental objectives, and project-specific aims.

Project & Financial Oversight

  • Facilitate contract execution by company signatories.

  • Monitor project financials, hours, and tasks, escalating discrepancies timely.

  • Ensure compliance with SOPs, Work Instructions (WIs), and timesheet records.


Qualifications

  • BA/BS in Business Administration, Public Administration, Public Health, or related field; advanced degree preferred.

  • Moderate contract management experience in CRO or pharmaceutical industry; management experience preferred.

  • Strong knowledge of clinical development processes, legal, and contracting parameters.

  • Proficient in Microsoft Office Suite.

  • Customer-focused with ability to manage priorities under pressure.

  • Excellent understanding of clinical trial processes across Phases II-IV and ICH GCP.

  • Good understanding of clinical protocols, study specifications, and site start-up processes.

  • Project management experience in a fast-paced environment.

  • Strong vendor management, organizational, negotiation, and problem-solving skills.

  • Ability to mentor and motivate junior staff.

  • Quality-driven, detail-oriented, and able to provide constructive guidance.


Get to Know Syneos Health

  • Worked with 94% of all Novel FDA Approved Drugs and 95% of EMA Authorized Products over the past 5 years.

  • Supported over 200 studies across 73,000 sites and 675,000+ trial patients.

  • Encourages initiative and challenges the status quo in a competitive, fast-paced environment.

Learn more: Syneos Health


Additional Information

  • Job duties may change at the company's discretion.

  • Equivalent experience or skills may be considered.

  • No part of this description creates an employment contract.

  • Complies with local and international employment legislation.

  • Reasonable accommodations provided per the Americans with Disabilities Act.


Summary

Roles within Site Start-Up/Site Identification manage and execute site identification processes in compliance with regulations, SOPs, and project requirements. Responsibilities include negotiating site agreements (CDAs, SIFs), maintaining and reporting site performance metrics, and serving as the primary point of contact for investigative sites. Individual contributors may manage lower-level staff or processes and contribute to the design, implementation, and delivery of departmental programs and policies.

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