Clinical Research Associate (CRA) - ATM/Credit Card Focus

Veeda Clinical Research
Applicants0
Posted2 days ago

Job Highlights

Experience0 - 6 Yrs
Salary9-11 LPA
LocationGurgaon
Work ModelRemote
RoleATM / Credit Card
Openings3
EmploymentFreelance
EducationAny Postgraduate

Required Skills

Clinical Trial MonitoringGCP ComplianceRegulatory AffairsSite ManagementData ManagementFinancial AcumenAttention to DetailProblem-SolvingCommunication SkillsInterpersonal SkillsProficiency in MS Office SuiteFamiliarity with clinical trial management systems (CTMS)Understanding of payment processing systems (ATM/Credit Card)

Job Description

Role Summary: We are seeking a diligent and detail-oriented Clinical Research Associate (CRA) to join our dynamic team. This specialized role will involve overseeing clinical trials with a unique focus on aspects related to ATM and credit card usage within the context of participant reimbursement, expense tracking, or other financial mechanisms relevant to study conduct. The CRA will ensure the integrity of trial data, adherence to protocols, and compliance with regulatory standards, while also managing the logistical and financial aspects related to participant compensation and site payments via ATM/credit card infrastructure.

Key Responsibilities:

  1. Conduct site visits (initiation, monitoring, close-out) to ensure study protocol adherence and data accuracy.
  2. Verify the accurate and timely disbursement of participant stipends/reimbursements using ATM/credit card systems, ensuring compliance with financial protocols.
  3. Manage and reconcile site expenses related to participant compensation and operational costs, particularly those processed via credit card transactions.
  4. Ensure all site financial records, including ATM withdrawal receipts and credit card statements, are meticulously maintained and compliant.
  5. Liaise with study participants, site staff, and internal teams regarding financial procedures and any discrepancies.
  6. Oversee the secure handling of any physical ATM cards or credit card information provided to participants or sites.
  7. Monitor study progress, identify potential risks, and implement corrective actions.
  8. Prepare and submit monitoring visit reports in a timely manner.
  9. Ensure compliance with Good Clinical Practice (GCP), FDA regulations, and other applicable local and international guidelines.

About Veeda Clinical Research

Veeda Clinical Research is a leading Contract Research Organization (CRO) based in India, dedicated to providing comprehensive clinical research services to the pharmaceutical and biotechnology industries. Established with a vision to accelerate drug development, Veeda offers end-to-end solutions from early-phase studies to late-phase clinical trials. Their expertise spans across various therapeutic areas, ensuring high-quality data and regulatory compliance. Veeda is committed to scientific excellence, ethical conduct, and timely delivery of projects, making them a trusted partner for global innovators seeking to bring life-saving therapies to market.

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