This is an exciting opportunity for an experienced Clinical Research Associate or Senior Clinical Research Associate to support the clinical development efforts of a respected international organisation. With a strong commitment to improving patient outcomes through high-quality research, they lead studies across diverse therapeutic areas, operating under rigorous standards that place patient safety and scientific integrity at the forefront. Contractors here play a crucial role in progressing meaningful studies, working with innovative methodologies that include on-site, remote and risk-based monitoring. Your role as Clinical Research Associate / Senior Clinical Research Associate Oversee investigational sites from start-up to close-out, delivering on-site, remote or hybrid monitoring in line with study timelines and protocols. Maintain clear, proactive communication with sites, project teams, and sponsors to keep studies running smoothly. Support study start-up activities, including site identification, feasibility assessments and selection. Deliver protocol training to site staff and ensure investigational products are correctly managed, stored and documented. Perform thorough source document review and verification, and collaborate on query resolution within EDC systems. Manage essential documents and ensure the completeness and accuracy of the site-level Trial Master File. Experience and qualifications for the Clinical Research Associate / Senior Clinical Research Associate role University degree or equivalent experience, ideally with a background in health sciences; advanced degrees welcome but not essential. Minimum of 3 years' experience as a CRA within pharmaceuticals, biotech or CRO environments. Strong grasp of GCP principles with proven ability to apply them in day-to-day monitoring. Familiarity with clinical study phases, local regulatory approval processes, and standard clinical systems (EDC, CTMS, eTMF, IXRS). Excellent communication skills, detail-focused, and adept at problem-solving to keep studies compliant and on track. Comfortable with extensive travel and overnight stays, holding a valid passport with at least six months remaining. For immediate consideration, or to learn more about similar contract opportunities in clinical research, apply today or reach out directly. #J-18808-Ljbffr SEC Life Sciences
...need to grow personally, express your individuality, and create change in your community. how youll make the difference Our bakeries are a hub of comfort and happiness in our Wegmans stores. As a member of our Bakery Department, youll work alongside a talented...
...Travel Nurse RN - NICU - Neonatal Intensive Care - $1,950 per week at TotalMed Staffing summary: A Travel Nurse Registered Nurse (RN) specializing in Neonatal Intensive Care Unit (NICU) provides... ...healthcare professionals in travel, PRN, and permanent positions across the...
...Overview HSM Spiller is looking for a CDL-A truck driver. No experience needed but must hold a CDL Class-A. At HSM Spiller we pride ourselves on being home weekly. Along with runs that last 2-3 days at a time. At HSM Spiller there is a 99% no touch freight along with...
...luxury automotive Collaborating with creative directors, art directors, copywriters, strategists, videographers and photographers, editors, designers, and animators: all in-house Working at the speed of social - fast! Which means more opportunities to make...
...detection, situation awareness systems, and communications equipment to aid in the apprehension of violators of state, federal, or immigration laws. Communicating assignments and training peers on the application of the appropriate law enforcement problem-solving...