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Caidya

Global CRO delivering end-to-end clinical development

Grants Specialist I

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRemote in IndiaNo salary listed

About the Job

Requirements

  • A college or university degree is required; a healthcare, life science, finance, or related degree is a plus, and an equivalent combination of education and relevant work experience may be considered.
  • Typically, at least four years of experience in clinical research, site payments, grant administration, finance, accounting, or a related function is required.
  • Experience coordinating site payments and working with global study teams is required.
  • Strong written and verbal communication skills in English are required.
  • Strong interpersonal skills and the ability to collaborate with global internal and external study teams are required.
  • Strong computer skills, including Microsoft Office and site payment systems, are required.
  • Knowledge of the clinical trial lifecycle is required.
  • Exceptional attention to detail and a consistent focus on quality are required.
  • Strong organizational skills and the ability to manage competing priorities and timelines are required.
  • The ability to work effectively in a dynamic and changing environment is required.
  • Honesty, trust, fairness, cooperation, self-control, and flexibility are expected.
  • Strong coordination, facilitation, problem-solving, and escalation skills are required.
  • The ability to interpret reports, identify issues, and coordinate appropriate remediation is required.
  • The ability to work independently within approved plans, procedures, and delegated authority is required.
  • The ability to work flexible hours to accommodate study team and sponsor requirements is required.
  • The ability to travel based on study and business need is required.
  • The role may require minor lifting of less than 30 pounds.

Responsibilities

  • Coordinate site payment activities across the lifecycle of assigned studies and serve as the primary site payment contact for the study team, with supervision and support.
  • Review and interpret site contracts, study protocols, schedules of assessments, and payment language to identify site payment requirements.
  • Work with clinical study teams to finalize negotiated site budgets and ensure payment tracking systems are configured according to contractual requirements and payment expectations.
  • Create and maintain budget templates, individual site budgets, payee information, and payment schedules in designated payment tracking and financial systems; coordinate with Project Management, Finance, Contracts, and Legal as necessary.
  • Track executed site contracts and follow up on missing payment-related documentation, including W-9s and other required administrative records.
  • Develop and maintain site payment forecasting models based on approved study budgets, country allocations, study assumptions, and current study circumstances; provide periodic estimates to support financial planning and reporting.
  • Perform quality control reviews of site budgets, invoices, payment schedules, and related grant information in designated systems.
  • Review, verify, and process site payments in collaboration with Project Management and Finance, ensuring accuracy, compliance with contractual requirements, and adherence to established timelines.
  • Respond to payment inquiries from study teams, sponsors, and sites; coordinate communications and issue resolution to support study priorities and timelines.
  • Code and maintain invoices and supporting documentation, and establish, maintain, and reconcile site financial records in accordance with applicable financial principles, company procedures, and sponsor requirements.
  • Prepare, manage, monitor, and reconcile grant payment accruals, including year-end accrual estimates, and partner with Finance on applicable financial reporting.
  • Provide site payment documentation and supporting records for audits and internal reviews as required.
  • Perform other related duties as assigned by departmental management.
  • May provide study-level task direction and technical guidance to Grants Coordinators on assigned studies.

Desired Qualifications

  • A healthcare, life science, finance, or related degree is a plus.

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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