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Seeking a Pharmacovigilance Associate to join the team. Responsibilities include reviewing and processing safety events, generating data listings, completing adverse event follow-up, supporting safety management, and liaising with stakeholders. The ideal candidate has 1 year of experience in pharmacovigilance, excellent communication skills, and is detail-oriented.

As a Study Start Up Associate II, responsible for feasibility, site identification, site contract negotiation, regulatory submissions, and preparing submissions to regulatory and ethics bodies. Requires a Bachelor's Degree, 2 years of experience in clinical study start up, fluency in local language and English, and strong organizational skills.

Exciting opportunity to join the global client contract services department at a leading CRO. Responsibilities include preparation, analysis, and finalization of contract cancellations and reconciliations. Requires 3-9 years of costing development experience and fluency in Excel.

ICON plc is seeking a Payroll Associate to assist in the global payroll cycle, ensuring accuracy in payroll inputs and outputs, managing internal controls, and meeting tax and compliance requirements. The role involves working under pressure, meeting strict deadlines, and providing high-quality customer service.

The Site Management Associate is responsible for managing eTMF uploads, vendor management, study budget preparation, and risk mitigation from study initiation to archiving. They ensure compliance with company standards and scientific requirements while facilitating communication and coordination within the project team.

Managing the Project Finance team to ensure high-quality delivery, financial analysis, and reporting. Responsible for project ownership, financial metrics analysis, and external reporting to sponsors. Develop and maintain financial forecasts and budget reconciliations for the business unit. Collaborate with Project Management group and support process improvement initiatives.

As a Study Start Up Associate I & II at ICON, you will play a key role in preparing physicians at research sites to start trials for new pharmaceutical and biological products. Responsibilities include reviewing contracts, negotiating budgets, and facilitating communication between stakeholders. Ideal candidates have 2-5 years of clinical research experience and knowledge of ICH GCP. Added advantage for those with international experience and proficiency in EC, IRB, and CA queries.