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Senior Site Contracts Manager

0-2 years
Not Disclosed
10 Oct. 2, 2025
Job Description
Job Type: Full Time Remote 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

🧾 Job Title: Senior Site Contracts Manager

🏢 Company: Ergomed PLC
📍 Location: Remote
🕒 Employment Type: Full-time
📂 Department: Site Contracts


🌍 About Ergomed

Ergomed PLC is a rapidly expanding full-service mid-sized CRO specializing in Oncology and Rare Disease, with operations in Europe, North America, and Asia.

  • Founded: 1997

  • Culture: International, collaborative, and employee-centric

  • Focus: Delivering high-quality clinical services while supporting employee growth and well-being


🧾 Job Description

The Senior Site Contracts Manager will oversee the negotiation and execution of clinical study agreements (CSAs/CTAs) for assigned trials and act as a subject matter expert for sponsors and stakeholders.

The role may also include people management responsibilities, mentoring, and professional development of team members.


🔹 Key Responsibilities

  • Oversee negotiations of clinical study agreements (CTAs), including contractual language, financial attachments, and investigator grant budgets

  • Manage contact and budget negotiation status and escalate out-of-parameter queries to sponsor decision-makers

  • Plan CSA execution strategy for assigned studies aligned with start-up delivery plans and client expectations

  • Prepare CSA templates, payment terms, fallback positions, and negotiation parameters in line with Ergomed standards

  • Lead CSA negotiations and ensure timely finalization and execution

  • Maintain document status reports and update department tools/systems regularly

  • Manage discussions with internal and sponsor stakeholders regarding fair market value of investigator budgets and payment terms

  • Build strong relationships with sponsors to ensure smooth negotiations and repeat business

  • Be accountable for Site Contracts delivery for assigned projects or initiatives

  • People management: may include interviewing, selection, terminations, professional development, performance appraisals, job descriptions, and employee counseling

  • Perform other work-related duties as assigned


🎓 Qualifications

  • BS degree in law, business, life sciences, health-related field, or equivalent combination of education and experience

  • Strong CRO operational experience with a track record in Site Contracts Management at an international or global level

  • Thorough knowledge of regulations, drug development, and clinical project management procedures

  • Understanding of country/site-specific requirements, particularly in North America

  • Proficient in MS Office (Word, Excel, PowerPoint), Outlook, and Internet

  • Strong presentation, documentation, and interpersonal skills

  • Ability to handle multiple tasks, deliver high-quality work independently, and meet deadlines

  • Attention to detail, effective oral/written communication skills, and leadership ability to mentor junior team members


🌟 Why Ergomed

  • Training and career development opportunities internally

  • Strong emphasis on personal and professional growth

  • Friendly, supportive working environment

  • Global collaboration with colleagues across multiple regions

  • Core values:

    • Quality

    • Integrity & Trust

    • Drive & Passion

    • Agility & Responsiveness

    • Belonging

    • Collaborative Partnerships

Ergomed fosters an inclusive, human-centric workplace where employees can grow, contribute, and make a positive impact on patient lives.