Clinical Research Associate 2

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ph3Who We Are /h3 pEmerald Clinical Trials is a bglobal leader /b in clinical research, partnering with over b160 biotech /b companies and b15 of the world's top 20 /b pharmaceutical firms.
Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases, offering bPhase I-IV and real-world studies /b.
/p pWith over b25 years of experience /b and a bworld-renowned focus in renal research /b, Emerald Clinical has helped drive medical breakthroughs through deep scientific insight, flawless execution, and an unwavering commitment to quality.
/p h3Global Expertise.
Local Insight.
Real Impact.
/h3 pEmerald Clinical is where science, speed, and strategy come together to transform healthcare.
For over 25 years, we have led the way in clinical research, combining global reach with deep Asia-Pacific expertise and unparalleled local insight to deliver smarter trials and stronger outcomes.
/p pOur b800+ employees that span across Asia-Pacific, Europe, and the Americas /b are embedded in communities worldwide.
We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward.
/p h3About The Role /h3 pThe Clinical Research Associate 2 (CRA2) is a member of the Clinical Operations group at bEmerald Clinical /b.
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 implementing project plans and to ensure compliance with regulatory requirements and Standard Operating Procedures (SOPs).
/p h3Your Responsibilities /h3 ul liCoordinate the identification, feasibility assessment, and selection of investigators and sites to undertake the trial.
/li liComplete all monitoring activities per the Monitoring Plan along with completing monitoring visit reports, accurately and within the predetermined timeframe.
/li liPrepare, plan, organize, and conduct site evaluation visits and report on these visits to assist in site selection.
/li liPrepare, submit, and/or liaise with regulatory specialist colleagues, regarding the preparation of regulatory packages, importation/exportation requirements, and updates of Ethics Committee packages.




/li liNegotiate site budgets, coordinate for site contract execution, track invoicing, and ensure timely site payments.
/li liPrepare, plan, organize, and conduct site initiation visits.
/li liDevelop and maintain appropriate monitoring tools and project-specific documents.
/li liMotivate 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.
Collect, review, and approve essential documents from trial sites, to ensure quality and compliance, and code documents for Trial Master File (TMF) filing.
/li liReconcile contents of in-house TMF and site's Investigator Site Files.
/li liCoordinate distribution, tracking, handling, and destruction of investigational product and other trial supplies per site/trial requirements.
/li liMaintain trial information using the clinical trial management system and any other tracking and reporting tools for the trial.
/li liSupport strategies to boost recruitment efforts.
/li /ul h3About You /h3 ul liQualifications in a related science or health care discipline.
/li liPrevious experience in clinical trials within an academic, CRO, or pharmaceutical environment with 2-5 experiences in on-site monitoring and site management experience is mandatory.
/li liDemonstrate practical knowledge of ICH-GCP guidelines and global and local ethical and regulatory research requirements.
/li liDisplay 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.
/li liDemonstrate competence in the following business skill areas:



negotiation and conflict resolution, critical thinking, problem-solving, decision making, and strategic thinking.
/li liDemonstrate solid interpersonal communication, presentation skills, and flexibility to work well within a multi-disciplinary team both autonomously and with a wide range of varying stakeholders.
/li liAbility to be flexible and adaptable in the face of changing organizational priorities and ambiguous environments.
/li liAbility and willingness to travel.
/li /ul h3Why Join Us?
/h3 pAt our core, bEmerald Clinical Trials /b 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.
/p h3Here's What Makes Us Stand Out /h3 ul liPurpose-Driven Work: You'll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology.
/li liGlobal Reach, Local Expertise: Our teams connect with local communities, building trust and meaningful engagement for every trial.
/li liCollaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges.
/li /ul h3What We Offer /h3 pWe understand that great work happens when people feel valued and supported.
That's why we provide: /p ul liCompetitive Compensation: A tailored salary and benefits package to reflect your skills and experience.
/li liFlexibility: Enjoy hybrid or remote working arrangements, depending on your location and role.
/li liCareer Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role.
/li liEmployee 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.
/li liGlobal Opportunities: Be part of a company with international reach, offering you exposure to diverse projects and clients.
/li /ul pWe are an equal-opportunity employer and encourage applications from all qualified candidates.
/p /p #J-*****-Ljbffr

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