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Caidya

Global CRO delivering end-to-end clinical development

Investigator Contracts Lead

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.
  • At least 3 years of contracts-related experience is required; experience in a contract research organization or pharmaceutical setting 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, applied to 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 International Council for Harmonisation Good Clinical Practice.
  • Ability to interact effectively and appropriately with investigative site personnel.
  • Strong organizational skills and attention to detail, with the ability to handle multiple tasks effectively.
  • Ability to identify site contract and budget issues early, communicate them clearly to internal and client project teams, draft appropriate resolutions, problem-solve, and work independently.
  • 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, Microsoft Excel, and Microsoft PowerPoint.
  • Exceptional written and oral English communication skills.
  • An advanced degree is preferred.
  • Legal education is preferred, such as paralegal certification or a Juris Doctor.

Responsibilities

  • Serve as Contract Lead for assigned countries and regions, participating in kick-off meetings and sponsor calls, and providing procedural and legal guidance, study updates, and advice to facilitate site contract execution.
  • Forecast intermediate clinical contract steps and oversee execution to achieve contractual milestones.
  • Manage Contracts Specialists and other project staff negotiating site contracts, ensuring they are included in the project and have access to applicable study systems and folders.
  • Create study-specific contract templates for assigned countries, either by drafting them directly or collaborating with assigned contract negotiators.
  • Work with the Project Manager and Sponsor to develop contract negotiation guidelines, 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 processes, and fair market value assessment procedures.
  • Forecast site contract execution dates and communicate timelines to stakeholders; oversee contract and budget status entries in applicable tracking systems.
  • Collaborate with contract negotiators to resolve site contract and budget negotiation impasses, including negotiating directly with study sites when appropriate.
  • Conduct fair market value assessments for budget items outside negotiation benchmarks, facilitating Sponsor approval or providing direct approval when authorized.
  • Serve as an internal escalation point for legal-language negotiations and approve contract terms when authorized.
  • Maintain and update country-specific contract templates in the Clinical Contracts template repository.
  • Support the development and creation of contracts-related departmental intelligence tools.
  • Mentor Clinical Contracts team members on complex contract issues.
  • Serve as a contracts subject matter expert within the department and across departments.
  • Conduct training when called upon.

Desired Qualifications

  • Clinical research, contracts, or related experience in a team-oriented environment.
  • Experience in a contract research organization or pharmaceutical setting.
  • Experience with industry benchmarking tools such as GrantPlan or GrantsManager.
  • Proficiency in an additional language.

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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