[All remote jobs](https://jobicy.com/jobs.md)[![Precision Medicine Group logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/f1277044-221.jpg)](https://jobicy.com/company/precision-medicine-group.md)[Precision Medicine Group](https://jobicy.com/company/precision-medicine-group.md) # Senior Contracts and Budget Associate Review the role, location requirements, compensation details, and application process before deciding whether this opportunity fits your next career move. [Apply for this job](#job-application)[View company](https://jobicy.com/company/precision-medicine-group.md)ShareRemote from[South Korea](https://jobicy.com/job-region/south-korea.md)SalaryUndisclosedDepartment[Legal & Compliance](https://jobicy.com/categories/legal.md)EmploymentFull TimeExperienceSeniorPublished21 Oct 2026Apply before20 Nov 2026Listing views62Application actions4Application toolkit ## Make your next move. Prepare your resume, explore your fit, and draft a cover letter for this opportunity. AI Summary ## The role, at a glance. Senior Contracts and Budget Associate will prepare, negotiate, track, and coordinate clinical research agreements and site budgets for a global CRO. The role covers confidentiality disclosure agreements, clinical trial agreements, amendments, vendor contracts, and associated execution workflows. It requires close coordination with internal clinical operations teams, sponsors, and research sites across North America and Europe. The successful candidate will maintain contract records, resolve negotiation issues, and keep stakeholders informed against study timelines. Prior clinical research, biotech, pharmaceutical, or contract-research experience is strongly preferred. ## Role DNA A quick view of the complexity, pace, ownership and collaboration implied by the job description. ### Job Complexity 4/5EasyHard ### Pace & Pressure 4/5RelaxedFast-paced ### Autonomy Level 4/5GuidedFull ownership ### Communication Load 5/5IndependentCollaborative AI insightThe position requires specialized knowledge of clinical-trial contracting, careful negotiation, and rigorous control of legally significant documentation. Multiple stakeholders, site budgets, and study deadlines create a high-detail, deadline-driven workload. ## Salary analysis Estimated compensation compared with the broader US market for similar roles. Estimated job median (per year)Market rate$80,000US market range (per year)$65k–$100k0$110.00k AI insightThe yearly pay period is inferred from the job context; it was not explicitly stated by the employer. No employer salary was disclosed. The yearly USD figures are AI estimates for a senior clinical-research contracts professional and are shown as an indicative market range, not verified employer compensation. ## Core skills Skills and capabilities most closely associated with this opportunity. [Clinical trial agreements](https://jobicy.com/jobs?search_keywords=Clinical%20trial%20agreements.md)[Contract negotiation](https://jobicy.com/jobs?search_keywords=Contract%20negotiation.md)[Confidentiality disclosure agreements](https://jobicy.com/jobs?search_keywords=Confidentiality%20disclosure%20agreements.md)[Site budget management](https://jobicy.com/jobs?search_keywords=Site%20budget%20management.md)[Contract lifecycle management](https://jobicy.com/jobs?search_keywords=Contract%20lifecycle%20management.md)[Clinical research](https://jobicy.com/jobs?search_keywords=Clinical%20research.md)[Vendor contracts](https://jobicy.com/jobs?search_keywords=Vendor%20contracts.md)[Stakeholder management](https://jobicy.com/jobs?search_keywords=Stakeholder%20management.md)[Document management](https://jobicy.com/jobs?search_keywords=Document%20management.md)[Contract compliance](https://jobicy.com/jobs?search_keywords=Contract%20compliance.md)[Clinical operations](https://jobicy.com/jobs?search_keywords=Clinical%20operations.md)[Sponsor communication](https://jobicy.com/jobs?search_keywords=Sponsor%20communication.md) Sample interview questionsDescribe your experience negotiating clinical trial agreements and their amendments.I review templates and site-proposed revisions against approved contracting standards, identify legal and operational risks, and negotiate practical language that protects the sponsor while enabling timely site activation. I document open items, approvals, and final terms so that execution is traceable. How do you manage competing agreement and budget deadlines across multiple studies? I maintain a prioritized tracker with key milestones, owners, dependencies, and escalation dates. I review it regularly with study teams, communicate risks early, and focus first on items that could delay site activation or critical study deliverables. What are key considerations when reviewing a site budget? I verify that procedures, pass-through costs, payment schedules, start-up fees, and amendment terms align with the protocol and approved budget assumptions. I also ensure that payment language is clear, internally approved, and consistent with the associated CTA. How would you handle a site that requests non-standard contractual language? I would clarify the site’s underlying concern, assess the legal and operational impact, and consult internal legal or operational stakeholders where needed. I would then propose approved alternative language or escalate the issue with a concise summary of risks and recommended options. How do you keep sponsors and internal teams informed during negotiations? I provide concise, regular status updates that identify completed actions, outstanding issues, responsible parties, expected timelines, and any decisions needed. This keeps stakeholders aligned and makes potential delays visible before they affect the study plan. Opportunity details ## About this role. Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease. Precision for Medicine is looking for a Senior Contracts and Budget Associate. Position Summary: Review, draft, negotiate and track a variety of legal agreements including confidentiality disclosure agreements (CDA), initial clinical trial agreements (CTA), amendments to the clinical trial agreements (CTA-A), site budgets and other various types of documents. Will work closely with the Clinical Operations study team and play an administrative role to ensure deliverables are in alignment with defined project timelines and expectations. Essential functions of the job include but are not limited to: • Prepare and negotiate Agreements/Amendments such as Confidentiality Disclosure Agreements (CDA), Clinical Trial Agreements (CTA) and Amendments (CTA-A), vendor contracts and site budgets. • Lead interactions with the North American and European internal study teams, as applicable • Lead interactions regarding the various agreements with the Site(s) • Lead interactions regarding assigned agreements with the Sponsor(s) • Work with supervisor and various internal/external stakeholders to resolve contractual issues. • Ensure adhered to company policies, procedures, and contracting standards. • Update relevant study team members and sponsors regarding the status of contract negotiations and execution. • Coordinate execution of the agreements • Support the maintenance of contract files and databases, including email and document archiving. • Other duties as assigned. Requirements : • Bachelor’s degree, or equivalent contract management experience preferably in a clinical research or similar industry setting • 3 years of relevant experience drafting, reviewing and negotiating agreements related to clinical research i.e. Non-Disclosure Agreements, Clinical Trial Agreements, etc. as well as management, control and tracking of the contract process. • Experience in contract research, life science, biotech or pharmaceutical industry is preferred. Preferred: • Equivalent contract management experience in a clinical research or similar industry setting • Experience in contract research, life science, biotech or pharmaceutical industry. 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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [myHR@precisionmedicinegrp.com](mailto:myHR@precisionmedicinegrp.com). Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at [myHR@precisionmedicinegrp.com](mailto:myHR@precisionmedicinegrp.com) so we can investigate and take appropriate action. Candidates must be legally authorized to work in the country of employment without employer sponsorship. Show more [Apply now >](https://jobicy.com/jobs/156134-senior-contracts-and-budget-associate.md) > Annual salary information is not provided for this position. 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