Content Moderator (1-3 Yrs)

Veeda Clinical Research
Applicants0
Posted17 days ago

Job Highlights

Experience1 - 3 Yrs
Salary9-11 LPA
LocationKolkata
Work ModelHybrid
RoleContent Moderator
Openings3
EmploymentFreelance
EducationB.Tech/B.E.

Required Skills

Content ReviewRegulatory Compliance (ICH-GCP)Attention to DetailAnalytical SkillsCommunication SkillsProblem-SolvingData VerificationDocument ManagementMicrosoft Office SuiteClinical Research Documentation

Job Description

Role Summary: We are seeking a meticulous and detail-oriented Content Moderator with 1-3 years of experience and a BBA/BBM background to join our team in Kolkata. The Content Moderator will be responsible for ensuring the accuracy, compliance, and appropriateness of various content types within our clinical research operations. This role requires a strong understanding of regulatory requirements and the ability to apply them consistently.

Key Responsibilities:
- Review and moderate diverse forms of content, including but not limited to, study protocols, informed consent forms, patient-facing materials, and internal documentation, to ensure adherence to regulatory guidelines (e.g., ICH-GCP, local regulations).
- Verify the accuracy and completeness of data presented in various documents and reports.
- Identify and flag any inconsistencies, errors, or non-compliance issues, and escalate them to the relevant stakeholders.
- Collaborate with clinical research associates, project managers, and data managers to resolve content-related queries and discrepancies.
- Maintain detailed records of moderation activities and outcomes.
- Assist in the development and refinement of content moderation policies and procedures.
- Stay updated with the latest regulatory changes and industry best practices relevant to clinical research documentation.

About Veeda Clinical Research

Veeda Clinical Research is a prominent Contract Research Organization (CRO) based in India. Established with a vision to provide high-quality clinical research services, Veeda has been instrumental in supporting pharmaceutical and biotechnology companies in bringing innovative therapies to market. The company offers a comprehensive suite of services across various phases of clinical trials, adhering to international regulatory standards and ethical guidelines. Veeda is committed to scientific excellence, operational efficiency, and client satisfaction, making it a trusted partner in the global drug development landscape.

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