Clinical Research Associate

Clinical Research Associate - Detalhes da Vaga. ● If you’re looking for a project-based career as a CRA, we’d love to have a preliminary conversation, connect with us to explore future opportunities!This is a pipeline opportunity for proactive candidates interested in joining a global leader in the life sciences industry. ●The Clinical Research Associate (CRA) is responsible for overseeing clinical trials and ensuring compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. ● The CRA monitors the progress of clinical studies conducted at investigative sites and ensures that data is collected, recorded, and reported accurately. ●Key Responsibilities:Conduct site visits (initiation, monitoring, and closeout) to ensure adherence to study protocols and regulatory requirements. ●Verify that study data and documentation are accurate, complete, and maintained according to GCP. ●Identify, resolve, and escalate site issues related to protocol compliance or subject safety. ●Act as the primary liaison between the sponsor and investigative sites. ●Review and collect essential documents for the Trial Master File. ●Train and support site staff on study procedures and protocol requirements. ●Ensure timely reporting of adverse events and deviations. ●Assist in subject recruitment and retention strategies. ●Prepare and maintain accurate monitoring reports and documentation. ●Communicate findings and follow-up activities to stakeholders. ●Qualifications:Bachelor’s degree in life sciences, pharmacy, or relevant field (required). ●Prior experience as a CRA or in clinical research (3-7 years)Knowledge of Good Clinical Practice (GCP) and relevant regulatory guidelines. ●Strong attention to detail and organizational skills. ●Effective written and verbal communication abilities. ●Ability to travel frequently. ●Preferred Skills:Familiarity with Electronic Data Capture (EDC) platforms. ●Problem-solving and conflict resolution. ●Ability to work independently and in a team environment. ●3-7 years as a CRAWhy Join?Opportunity to join a globally recognised life sciences company through Kelly’s FSP model. ●Work with international experts on high-impact projects. ●Gain global exposure and expand your clinical knowledge. ●Be part of a collaborative, growth-focused work culture. ●Pipeline opportunity with anticipated hiring in the near future, apply early to be considered once the position is formally approved and released. ●. Requisitos para participar do processo. ● . O que oferecemos.