Senior Clinical Research Associate Fsp (Remote) Senior Clinical Research Associate Fsp | George Clinical |Australia A number of exciting new roles have arisen within our growing ClinicalOperations team! New Projects have resulted inopportunities arising for well-experienced Senior... A number of exciting new roles have arisen within our growing ClinicalOperations team! New Projects have resulted inopportunities arising for well-experienced SeniorClinical Research Associates to join us.You will be working on exciting new FSP projects with regional and/orglobal teams in a CRO that truly has an impact on improving the health ofmillions worldwide.Who are we?A leading global clinical research organization founded in Asia-Pacificdriven by scientific expertise and operational excellence20+ years of experience, 500+people managing 39+ geographical locationsthroughout the Asia-Pacific region, USA, and EuropeFull range of clinical trial services to biopharmaceutical, medicaldevice, and diagnostic customers, for all trial phases, registration andpost-marketing trialWe combine scientific leadership and global operational excellence,with strong experience in renal medicine, oncology, cardiovascular andchronic diseases to improve the health of millions worldwide.Why work with us?We are a global team, making a social impact Competitive market salary and benefitsFlexible and agile working arrangements – onsite, hybrid or WFH(dependent on location)Strong and diverse Learning & Development opportunities includingexposure to scientific leadership A focus on employee wellbeing including global employee engagementsurveys, steps challenges, reward and recognition programs, team buildingactivities and other fun events!About the role:Prepare, organise, conduct and follow-up routine monitoring and closeout visits as per relevant study planMotivate and train investigators and site staff to ensure obligationsin regards to study timelinesEnsure ethics submissions are made by investigator sites in a timelymannerAdherence to ICH-GCP and any other regulatory guidelines andrequirements including adverse events and serious adverse eventreportingCompliance with mandatory SOPs as agreed for the studyComplete all reports accurately and within the predeterminedtimelines.About you:Experience in a similar role within a CRO and/or PharmaceuticalcompanyExcellent co-ordination and time management capabilities including theability to prioritise demandsTertiary qualifications in Science or a relevant area preferredStrong interpersonal skills including the ability to communicate wellwith various types of peopleExcellent verbal and written communication skillsProficiency in the use of the Microsoft Office suite of products.We are searching for individuals who are results oriented and able tohandle rapidly changing priorities in a fast-moving environment. You mustbe willing to extend yourself and take on new challenges while living ourvalues of Mutuality, Integrity, Can-do approach, Empowermentand Excellence.How do I apply?Apply via LinkedIn or send your CV, referral or confidentialquery to and our friendly HR team across theworld will reach out as appropriate soon.Follow us on Linkedin to learn more about your future with GeorgeClinical.We are reviewing applications as we receive them but please notethat only short-listed applicants will be contacted.Thank you for your interest in working with George Clinical. As a globalbusiness, we are committed to handling Personal Information in accordancewith applicable privacy and data protection laws in the many countries inwhich we do business. Please see our Privacy Policy for furtherinformation.PrivacyPolicy Show more Show lessTagged as: remote, remote job, virtual, Virtual Job,virtual position, Work at Home, work from home When applying state you found this job on Pangian.com Remote Network. #J-18808-Ljbffr
