Join to apply for the Senior Clinical Research Associate role at Emerald Clinical6 days ago Be among the first 25 applicantsJoin to apply for the Senior Clinical Research Associate role at Emerald ClinicalGet AI-powered advice on this job and more exclusive features.At Emerald Clinical, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post-marketing.Our therapeutic expertise spans renal, cardiometabolic, and oncology—areas where we make a significant impact on improving global health.At the heart of our success is our ability to combine global reach with local knowledge. Our on-the-ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment. By prioritizing people, we deliver better engagement, more accurate data, and faster results—bringing therapies to patients in need.Why Join Us?At our core, Emerald Clinical is committed to transforming clinical research by putting people first—both patients and our employees. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide.Here’s What Makes Us Stand OutPurpose-Driven Work: You’ll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology.Global Reach, Local Expertise: Our teams connect with local communities, building trust and meaningful engagement for every trial.Collaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges.About The RoleThe Senior Clinical Research Associate (SCRA) is a member of the Clinical Operations group at Emerald Clinical. The Clinical Operations group is responsible for site management, monitoring tasks, and the operational support of clinical trials. The group allocates resources to projects as appropriate to assist with the implementation of project plans and to ensure compliance with regulatory requirements and Standard Operating Procedures (SOPs).Your ResponsibilitiesCoordinate the identification, feasibility assessment, and selection of investigators and sites to undertake the trial.Complete all monitoring activities per the Monitoring Plan along with completing monitoring visit reports, accurately and within the predetermined timeframe.Prepare, plan, organize, and conduct site evaluation visits and report on these visits to assist with site selection.Prepare, submit, and/or liaise with regulatory specialist colleagues, regarding the preparation of regulatory packages, importation/exportation requirements, and updates of Ethics Committee packages.Negotiate site budgets, coordinate for site contract execution, track invoicing, and ensure timely site payments.Prepare, plan, organize, and conduct site initiation visits.Develop and maintain appropriate monitoring tools and project-specific documents.Motivate and train investigators to ensure that the trial site personnel have a good understanding of the protocol, investigational product, and requirements of the trial so they can fulfill their obligations to conduct the trial accurately and to deadlines.Manage trial sites utilizing both on-site and off-site activities including: o Verification of quality, accuracy, completion, and timeliness of data.Reconcile contents of in-house TMF and site’s Investigator Site Files.Coordinate distribution, tracking, handling, and destruction of investigational product and other trial supplies per site/trial requirements.Maintain trial information using the clinical trial management system and any other tracking and reporting tools for the trial.Support strategies to boost recruitment efforts.Coordinate and perform translation verification of regional language, as required or as applicable per region.Perform site close-out visits and other site activities including archiving, as applicable.Mentor, coach, and train junior staff members as directed by line management.Perform any additional responsibilities assigned by the Line Manager and/or Project Lead.About YouEducated to degree level in pharmacy, medical, nursing, biological science, or other health-related disciplines preferred or equivalent relevant experience.≥5 years’ experience preferred, but ≥4 years may be considered based on relevant experience in clinical trial monitoring and/or site management within an academic, contract research organization, or pharmaceutical environment.Displays high competence in the following technical areas: ethical and participant safety considerations, site start-up management, site conduct management, risk management, quality management, supply management, scientific concepts and clinical research design, and issue escalation management.Demonstrate high competence in the following skill areas: negotiation and conflict resolution, critical thinking, problem-solving, decision making, and strategic thinking. Ability and willingness to travel.Ability to be flexible and adaptable in the face of changing organizational priorities and ambiguous environments.What We OfferWe understand that great work happens when people feel valued and supported. That’s why we provide:Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience.Flexibility: Enjoy hybrid or remote working arrangements, depending on your location and role.Career Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role.Employee Wellbeing: Participate in programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events.Global Opportunities: Be part of a company with international reach, offering you exposure to diverse projects and clients.Interested? Apply now and help us achieve our mission to improve the health of millions worldwide.Seniority levelSeniority levelMid-Senior levelEmployment typeEmployment typeFull-timeJob functionJob functionResearch, Analyst, and Information TechnologyIndustriesPharmaceutical ManufacturingReferrals increase your chances of interviewing at Emerald Clinical by 2xGet notified about new Senior Clinical Research Associate jobs in Sydney, New South Wales, Australia.Local Study Associate Director - BiopharmaMacquarie Park, New South Wales, Australia 6 days agoNorth Ryde, New South Wales, Australia 1 week agoClinical Project Manager II or higher AustraliaSydney, New South Wales, Australia 4 days agoAssociate Director, Country Operations Manager (Clinical Research)Macquarie Park, New South Wales, Australia 14 hours agoClinical Education Academic in Small Animal ECCSydney, New South Wales, Australia A$122,830.00-A$229,523.00 2 weeks agoMacquarie Park, New South Wales, Australia 5 days agoSydney, New South Wales, Australia 3 weeks agoSydney, New South Wales, Australia 3 weeks agoSenior / Clinical Research Associate (Sydney, Cell Therapy)Clinical Research Associate - CRA Australia (Level Depending on Experience)Research Assistant, Multiple positions (Centre for Molecular Oncology)Greater Sydney Area A$120.00-A$180.00 3 weeks agoSydney, New South Wales, Australia 5 days agoNorth Sydney, New South Wales, Australia 1 month agoSydney, New South Wales, Australia 2 weeks agoSydney, New South Wales, Australia A$80,000.00-A$90,000.00 3 weeks agoResearch Assistant-School of Public HealthSydney, New South Wales, Australia A$80,000.00-A$80,000.00 3 weeks agoSydney, New South Wales, Australia A$86,000.00-A$91,000.00 2 weeks agoClinical Research Coordinator - Oncology - St George HospitalSenior Clinical Research Associate (GC CRO)Senior Clinical Research Associate (GC CRO)North Ryde, New South Wales, Australia 1 week agoSt Leonards, New South Wales, Australia 2 weeks agoResearch Assistant FPIES/Allergy - REQ566147Westmead, New South Wales, Australia 2 weeks agoSydney, New South Wales, Australia 3 weeks agoClinical Project Coordinator / CTA for our office in Sydney / Australia (level dependent on experienSt Leonards, New South Wales, Australia 5 days agoSydney, New South Wales, Australia 2 weeks agoPostdoctoral Research Associate (Imaging)Sydney, New South Wales, Australia 3 weeks agoBaulkham Hills, New South Wales, Australia $61,638.00-$70,000.00 2 weeks agoWe’re unlocking community knowledge in a new way. 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