6 Onsite Monitoring Jobs

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data. What You Will Be Doing Working independently and actively to coordinate all activities for setting up and monitoring a study, completing...

Job Summary LTM is responsible and accountable for deliverables of studies assigned to RCO unit, performing end to end study related onsite/ remote monitoring, quality data review, essential documents management for studies managed in-house with-in agreed timelines, budget and desired quality standards. LTM is expected to adhere to required standard operating procedures, regulatory requirements, ICH GCP and quality in compliance with Sun Procedural Documents. Area Of Responsibility Ensures clinical trials are conducted at assigned sites as per protocol, local regulatory requirements, ICH GCP, ensure data integrity, patient safety and trials are conducted as per ethical standards (declaration...

As a Lead Trial Manager (LTM) at the RCO unit, you will be responsible for the successful delivery of studies assigned to you. Your role will involve performing end-to-end study-related onsite and remote monitoring, ensuring quality data review, and managing essential documents for in-house studies within agreed timelines, budget, and quality standards. Your key responsibilities will include: - Ensuring that clinical trials are conducted at assigned sites in compliance with the protocol, local regulatory requirements, ICH GCP, and ethical standards - Acting as the primary communication point between SPIL and clinical trial sites for site management activities - Facilitating regulatory submis...

Responsibilities & functions: Clinical Research Associate Working in accordance with ICH E6 principles and with applicable SOPs (either ECRON AcuNova or Sponsor's SOPs) & local regulatory norms. Review of study synopsis. Site selection. Preparation of Site feasibility questionnaire, conducting the feasibility and reporting to PM. Preparation, conduct and reporting of site selection visits. Negotiation & obtaining Investigator agreement on site budget, payment to the sites. Development/Local adaptation of study specific documents (ICF, CRF prints, Study logs), translations of the documents. Procuring essential documents from sites, their QC and filing in a timely manner and updating project t...

You will be joining Adani Airports Holding Limited as an Executive - Electrical, where your main responsibility will be to implement electrical design plans for airport construction projects. You will work closely with consultants, vendors, architects, and internal teams to ensure that all technical specifications and project requirements are met. This involves monitoring and documenting project costs, resolving technical issues, and ensuring that electrical installations comply with design specifications, safety regulations, and energy efficiency standards. Your role will also include conducting on-site inspections to track progress and validate system performance to contribute to the succe...

Position: Project Manager Clinical Trials Company: JSS Medical Research Location: Chennai Work Mode: Hybrid Job Description We are inviting applications for the role of Project Manager for clinical trials conducted PAN India. Key Responsibilities Lead and manage end-to-end clinical trial projects across India. Coordinate with internal teams, trial sites, and sponsors. Ensure project deliverables are met within timelines and budgets. Oversee site performance and address operational challenges. Provide leadership and guidance to Clinical Research Associates (CRAs). Maintain comprehensive and compliant study documentation. Preferred Candidate Profile Minimum 2 years of experience as a Project M...