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Caidya

Global CRO delivering end-to-end clinical development

Investigator Contracts Lead - Insourced to MNC

Contract ManagementConfirmed live in the last 24 hours
Full-timeChinaNo salary listedIn-person

About the Job

Requirements

  • A Bachelor of Arts or Bachelor of Science degree in a related field is required; an advanced degree is preferred.
  • Paralegal certification or a Juris Doctor is preferred.
  • At least 3 years of contracts-related experience is essential; clinical research, contracts, or related experience in a team-oriented environment is preferred, and CRO or pharmaceutical experience is strongly preferred.
  • A strong understanding of contracting principles and requirements is required.
  • Familiarity with budget development, benchmarking practices, and fair market value principles is required.
  • Proficiency in general and regionally specific contract fundamentals, with the ability to apply this knowledge to contract drafting, review, negotiation, and amendment processes.
  • Ability to handle multiple tasks and meet deadlines in a dynamic environment.
  • Understanding of clinical trial processes across Phases II–IV and ICH Good Clinical Practice, and ability to interact effectively with investigative site personnel.
  • Organizational skills and attention to detail, including the ability to handle multiple tasks effectively.
  • Ability to identify and understand site contract and budget issues early, communicate them concisely to internal and client project teams, draft responses to resolve them, problem-solve, and work independently using initiative.
  • Sound judgment and willingness to make timely decisions.
  • Ability to prioritize and plan work, use time efficiently, develop realistic action plans, and learn relevant new skills.
  • Proficiency with Windows, Microsoft Word, Excel, and PowerPoint.
  • Exceptional written and oral English communication skills; proficiency in another language is advantageous.
  • Strong personal interaction skills.

Responsibilities

  • Act as Contract Lead for assigned countries and regions, participate in kick-off meetings and sponsor calls, provide clients with procedural and legal guidance, and advise on study updates and ways to expedite site contract execution.
  • Forecast intermediate Clinical Contract steps and oversee execution to achieve contractual milestones.
  • Manage Contracts Specialists and other staff negotiating site contracts on the project, and ensure they have access to applicable study systems and folders, including Egnyte, D365, eTMF, and study-startup systems.
  • Create study-specific contract templates for assigned countries, by drafting them directly or collaborating with assigned contract negotiators.
  • Work with the Project Manager and Sponsor to develop contract negotiation guidelines and parameters, escalation pathways, and sponsor-specific signature requirements.
  • Work with the Project Manager, Grants Administration, Sponsor, and local Country Experts to develop country-specific site budget templates, negotiation benchmarks, escalation procedures, and fair market value assessment procedures.
  • Forecast site contract execution dates and communicate timelines to stakeholders to support timely site activation; oversee site contract and budget status entries in applicable tracking systems.
  • Collaborate with contract negotiators to resolve site contract and budget negotiation impasses, including directly negotiating contracts and budgets with study sites when appropriate.
  • Conduct fair market value assessments of budget items outside negotiation benchmarks, facilitating Sponsor approval or providing direct approval when authorized.
  • Serve as an internal escalation point to resolve legal-language negotiations and approve contract terms when authorized.
  • Maintain and update country-specific contract templates in the Clinical Contracts CTA template repository.
  • Support development and creation of contracts-related departmental intelligence tools.
  • Mentor Clinical Contracts team members on complex contract issues and serve as a contracts subject-matter expert within the department and across departments.
  • Conduct training when called upon.

Desired Qualifications

  • Experience in clinical research, contracts, or a related area in a team-oriented environment.
  • Experience in a CRO or pharmaceutical setting.
  • An advanced degree.
  • Legal education, such as paralegal certification or a Juris Doctor.
  • Experience with industry benchmarking tools such as GrantPlan or GrantsManager.
  • Proficiency in a language in addition to English.

About the Company

Caidya

Global CRO delivering end-to-end clinical development

Caidya is a global contract research organization that provides outsourced clinical development services for biopharmaceuticals and medical devices. It covers pre-IND strategy, early- and late-stage trials, regulatory submissions, and post-marketing surveillance, offered through flexible models like standalone projects, full-service partnerships, and FSP arrangements. Its Clarity platform combines data from multiple systems for near real-time trial visibility and it integrates with Medidata Rave and Veeva to support trial delivery. The merged heritage of Clinipace and dMed Global, led by Dr. Lingshi Tan, gives a broad North America–Asia-Pacific footprint and deep expertise in oncology, rare diseases, cell and gene therapy, dermatology, and cardiology, with the goal of helping clients bring therapies to market efficiently and compliantly.

Company size
201-500
Company stage
Growth Equity (Non-Venture Capital)
Total funding
$322.2M
Headquarters
Morrisville, NC
Founded
2003

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