Clinical Contracts Associate

Plano, TX, US • Posted 6 hours ago • Updated 6 hours ago
Full Time
No Travel Required
On-site
Depends on Experience
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Job Details

Skills

  • Clinical Contracting
  • Clinical Trial Budget Negotiation
  • Contract Negotiation
  • Contract Review & Redlining
  • Contract Amendments
  • Site Agreements
  • Clinical Research
  • GCP
  • ICH
  • GLP
  • Contract Law
  • Legal Terminology
  • Informed Consent Review
  • Regulatory Compliance
  • Clinical Trial Compliance
  • Sunshine Act/Open Payments
  • FWA Compliance
  • Human Subject Protection
  • Clinical Trial Insurance
  • Risk Identification & Mitigation
  • Stakeholder Management
  • Cross-Functional Collaboration
  • Analytical & Problem-Solving Skills
  • Negotiation Skills
  • Written & Verbal Communication
  • Microsoft Word
  • Microsoft Excel

Summary

Greetings!


Role:Clinical Contracts & Budget Associate

Location: United States – Plano, TX | Maple Grove, MN | Sylmar, CA
Department: Clinical Operations / Clinical Contracting
Employment Type: Full-Time

Position Summary

The Clinical Contracts & Budget Associate provides technical and operational support in the development, negotiation, review, execution, and processing of clinical study and research contracts, amendments, and complex study budgets.

Working under minimal guidance and supervision, the position collaborates with internal and external stakeholders to negotiate routine contractual and financial terms, resolve contract and budget issues, and ensure activities are completed accurately and within established timelines and study milestones.

The role requires an understanding of clinical research operations, business drivers, contractual requirements, compliance obligations, and applicable industry regulations. The incumbent will also support informed consent review, identify potential contractual and budget compliance risks, and provide appropriate guidance to study teams.

Key Responsibilities

  • Develop, review, negotiate, and process clinical study contracts, amendments, agreements, and complex clinical trial budgets with research sites and external partners.
  • Conduct routine contract and budget negotiations with limited supervision.
  • Collaborate with Clinical Operations, Legal, Finance, Procurement, and external site partners to resolve contract and budget issues.
  • Ensure contract and budget activities are completed within established timelines, metrics, and study milestones.
  • Review informed consent documents for alignment with clinical contracts and agreements and provide guidance to study teams.
  • Review and redline contractual documents in accordance with company policies, procedures, and established precedents.
  • Identify potential contractual, financial, and compliance risks and support timely risk mitigation.
  • Ensure required site and study information is complete and maintained to support regulatory and government requirements.
  • Support compliance with Google Cloud Platform, ICH, GLP, applicable federal and state regulations, company policies, and industry standards.
  • Maintain accurate contract, budget, and study documentation in applicable systems.
  • Provide timely follow-up on outstanding contract and budget activities.
  • Escalate complex contractual, financial, or compliance matters to appropriate stakeholders.
  • Handle sensitive and confidential information with appropriate discretion.
  • Support continuous improvement of clinical contracting and budget processes.

Required Qualifications

  • Associate degree or equivalent combination of education and relevant experience.
  • Minimum 1–2 years of relevant experience in clinical research, clinical contracting, contract administration, budgeting, legal operations, or a related field.
  • Strong written and verbal communication skills.
  • Strong analytical, organizational, problem-solving, and follow-up skills.
  • Ability to manage multiple priorities and meet deadlines.
  • Proficiency with Microsoft Word and Excel.

Preferred Qualifications

  • Bachelor's degree in Business Administration, Life Sciences, Healthcare Administration, Legal Studies, or a related field.
  • 3–5 years of experience in clinical contracts, clinical trial budgets, contract administration, or a related function.
  • Experience in a pharmaceutical, biotechnology, medical device, CRO, or other life sciences organization.
  • Sponsor-side clinical contracting experience preferred.
  • Paralegal certificate or relevant legal/contract training preferred.
  • Experience negotiating and redlining clinical trial agreements and site budgets.
  • Knowledge of contract law and fundamental legal terminology.
  • Familiarity with clinical research regulations and industry standards, including Google Cloud Platform, ICH, GLP, Sunshine Act/Open Payments, FWA, Human Subject Protection, and clinical trial insurance requirements.
  • Experience working with cross-functional teams and external research sites.

Core Competencies

  • Clinical Contracting & Budget Negotiation
  • Contract Review & Redlining
  • Clinical Research Compliance
  • Risk Identification & Mitigation
  • Stakeholder Management
  • Analytical & Problem-Solving Skills
  • Written & Verbal Communication
  • Organization & Time Management
  • Attention to Detail
  • Confidentiality & Professional Judgment

Work Locations

  • Plano, Texas
  • Maple Grove, Minnesota
  • Sylmar, California
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 91163707
  • Position Id: 9076567
  • Posted 6 hours ago

Company Info

About Siro Clinpharm Pvt Ltd

Founded in 1996 as the SIRO Research Foundation and incorporated in 2000 as SIRO Clinpharm Private Limited, SIRO brings over two decades of exceptional project management expertise to the table. From pioneering proof-of-concept trials to managing complex, multinational studies involving rare diseases, stringent protocols, and accelerated timelines, SIRO has consistently delivered with precision and reliability. Our win-win philosophy drives us to ensure success for every client. Today, SIRO stands as a leading provider of drug development and discovery solutions, offering a diverse and innovative suite of CRO services to global biotech, pharmaceutical, medical device, and academic institutions. To better serve our clients’ evolving needs, we have strategically reorganized into three specialized entities: SIRO Clintech, SIRO Medical Writing, and SIRO Clinpharm, which continues to offer specialized FSP services.
 
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AM

Akhilesh Mishra

Recruiter @ Siro Clinpharm Pvt Ltd
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