Contract Analyst II

2 - 7 years

5.0 - 6.0 Lacs P.A.

Chennai, Trivandrum, Bengaluru

Posted:2 months ago| Platform: Naukri logo

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Skills Required

AssuranceContract managementAnalyticalPharmaLegalClinical trialsclinical developmentClinical researchHealthcareAnalyst II

Work Mode

Work from Office

Job Type

Full Time

Job Description

As a Site Contract Analyst II at ICON, you will be working within a large-scale, fast-paced environment, supporting the Study Start Up Team Lead in developing and executing the plan for country and site distribution. Your expertise and dedication will be essential in efficiently conducting SSU (Study Start Up) activities in the assigned countries, ensuring the smooth initiation and progress of clinical trials. What you will be doing Efficiently Drive Study Initiation: review and negotiate clinical site investigator contracts and budgets. Maintain communication with Investigative sites, sponsors and internal personnel regarding the status of contracts and contract-related documents. Reviewing and analysing contracts, agreements, and legal documents related to clinical trial activities and vendor relationships. Negotiating contract terms and conditions with clients, vendors, and other stakeholders to ensure compliance with regulatory requirements and company policies. Collaborating with cross-functional teams to assess contract risks, identify opportunities for improvement, and develop strategies to mitigate potential issues. Maintaining accurate and up-to-date records of contract status, milestones, and deliverables using contract management systems. Providing guidance and support to internal teams on contract-related matters, including contract interpretation, compliance, and dispute resolution. Your profile Bachelors degree in Business Administration, Legal Studies, or a related field; advanced degree or certification in Contract Management or a relevant discipline preferred. Minimum of 2 years of experience in contract administration, contract management, or a related field, preferably in the pharmaceutical or clinical research industry. Strong understanding of contract law, legal terminology, and regulatory requirements related to clinical trials and vendor agreements. Excellent analytical and problem-solving skills, with the ability to evaluate complex contractual issues and propose effective solutions. Strong attention to detail and organizational skills, with the ability to manage multiple tasks and prioritize work effectively in a fast-paced environment.

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St Albans Hertfordshire

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