Underwriter role in Clinical Research / Contract Research (3-4 Yrs)

Veeda Clinical Research
Applicants0
Posted27 days ago

Job Highlights

Experience3 - 4 Yrs
Salary1-6 LPA
LocationBangalore
Work ModelRemote
RoleUnderwriter
Openings1
EmploymentPart-Time
EducationAny Graduate

Required Skills

Risk AssessmentFinancial AnalysisContract ReviewClinical Trial ManagementRegulatory Compliance (ICH-GCP)Attention to DetailAnalytical SkillsProblem-SolvingCommunication SkillsTeamworkNegotiation SkillsMicrosoft Excel

Job Description

Role Summary: We are seeking a detail-oriented and analytical Underwriter with 3-4 years of experience to join our team in Bangalore. The Underwriter will be responsible for assessing and managing risks associated with clinical trial services, ensuring compliance with company policies and regulatory requirements. This role requires a strong understanding of the clinical research landscape and the ability to make informed decisions.

Key Responsibilities:

Review and analyze clinical trial proposals, contracts, and budgets to assess financial and operational risks.

Determine the feasibility and profitability of potential projects based on risk assessment.

Collaborate with business development, legal, and operational teams to structure proposals and contracts.

Ensure all underwriting activities comply with relevant industry regulations (e.g., ICH-GCP) and internal guidelines.

Monitor and manage risks throughout the lifecycle of a clinical trial project.

Prepare underwriting reports and present findings to senior management.

Stay updated on industry trends, market conditions, and regulatory changes impacting clinical research.

About Veeda Clinical Research

Veeda Clinical Research is a leading Indian Contract Research Organization (CRO) founded in 2011. Headquartered in Ahmedabad, Gujarat, Veeda provides a comprehensive range of clinical research services to the pharmaceutical and biotechnology industries. Their expertise spans across various therapeutic areas, with a strong focus on early-phase clinical trials (Phase I/IIa) and bioequivalence studies. Veeda is committed to delivering high-quality, cost-effective, and timely clinical development solutions, adhering to global regulatory standards. They aim to be a preferred partner for drug development by leveraging scientific expertise and robust operational capabilities.

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