Responsibilities: *To acquire knowledge and skills to process study documents in accordance with client and study requirements as per study-specific processes, ICON SOPs/WPs and regulations, where applicable.• *To acquire knowledge and skills to complete activities related to document receipt and ...
Clinical Research Jobs Latest Articles
Regulatory Affairs Associate I
ClinicalresearchinfoThe opportunity Regulatory Affairs associate I – RA publishing will participate in the publishing of different regulatory activities. The focus will be to ensure 100% quality and timeline of the submission. This role will be the primary interface with the ...
Study Start Up Associate I & II /Senior SSUA
ClinicalresearchinfoStudy Start Up Associate IIAs a member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological ...
Pharmacovigilance Systems Specialist
ClinicalresearchinfoJob Description: The employee is expected to demonstrate the ICON leadership competencies.Gather and document user requirements specific to ongoing Pharmacovigilance systems projects.Guides User Acceptance Testing and assumes the role of the SME on behalf of the Safety Team.Provides systems expertise ...
Pharmacovigilance Reporting Associate
ClinicalresearchinfoSubmission of expedited Serious Adverse Event (SAE) reports, Periodic reports, line listings and applicable safety information to clients, Regulatory Authorities, Ethics Committees, investigators, third party vendors, Partners, and ICON personnel, if required & as agreed with client during study set-up, ...
Clin Ops Specialist
ClinicalresearchinfoJob responsibilities•   Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions •   Assists Clinical Monitoring staff with site management activities, including serving as a Sponsor representative for sites on assigned studies, ...
Project Coordinator-Medical Affairs
ClinicalresearchinfoAs healthcare providers are deluged with data and are making choices in an increasingly complex and stressed health system, Lilly Medical Affairs provides clear, credible answers that will set Lilly apart from its competitors. Medical Affairs’ mission is to make ...
Medical Writing Associate I
ClinicalresearchinfoLiterature search, preparation of Clinical study protocols and PSP according to required day to day Guidelines and Regulatory Requirements by using Product Monographs/Prescribing Information/Summary of Product Characteristics etc., as applicable.Preparation of Informed Consent Form/s (ICF) in line with Clinical study ...
Clinical Research Associate
ClinicalresearchinfoWhat you will be doing: Performing monitoring visits according to plan, document actions and follow up on action plansSite feasibility visits incl. analysis of site logistics, site personnel performance/quality indicators and accountability for patient recruitment strategiesTrain and guide site staff ...
Trainee – 0-1 experience in a manufacturing
ClinicalresearchinfoDivision Quality Department Formulation Sub Department 1 Formulation – Quality Control Job Purpose Execute the production operations in line with safety and GMP requirements to meet the manufacturing targets in shift. Key Accountabilities (1/6) Operate the equipment efficiently without error ...