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Experience, qualification, and soft skills, have you got everything required to succeed in this opportunity Find out below.
Emerald Clinical Trials is a
global leader
in clinical research, partnering with over
160 biotech
companies and
15 of the world’s top 20
pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end‑to‑end clinical trial solutions across all phases, offering
Phase I‑IV and real‑world studies .
With over
25 years of experience
and a
world‑renowned focus in renal research , Emerald Clinical has helped drive medical breakthroughs through deep scientific insight, flawless execution, and an unwavering commitment to quality.
Global Expertise. Local Insight. Real Impact.
Emerald 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.
Our
800+ employees that span across Asia‑Pacific, Europe, and the Americas
are embedded in communities worldwide. We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward.
About The Role
The Project Manager is responsible for the development, conduct and completion of research projects in accordance with the reasonable requirements of the originator of the project. The Project Manager oversees all aspects of study management activities including cross‑functional team leadership and coordination, client communication/management, financial management and overall study delivery. The Project Manager must ensure studies are resourced effectively, managed efficiently, achieve project objectives within allocated budgets and agreed timelines, and are conducted to the highest standards of Good Clinical Practice (GCP), regulatory requirements and applicable Standard Operating Procedures (SOP). The Project Manager mentors and coaches junior project management staff or Clinical Delivery Leads and assists their technical development. Manage independently or with support from Portfolio Delivery Leads or Line Manager.
Your Responsibilities
All activities must be conducted in accordance with project specific documentation, applicable SOPs, ICH GCP and applicable regulatory requirements.
Maintain effective professional relationships with external customers, investigators and vendors. Maintain effective professional relationships with internal project team including those providing academic input.
Project Kick‑off
Attend relevant project specific meetings including formal kick‑off meetings.
Develop project plan and other internal project management documents. Assist the originator of the project in the development of project specific documents such as protocol and participant information forms as requested.
Project Implementation and Closure
Manage the implementation, ongoing evaluation, prioritisation, reporting and timely delivery of all operational aspects of allocated project/s including:
Contribute to the preparation of project specific budget where applicable.
Track budget for allocated portion of project.
Deliver relevant portion of project specific budget by guiding team and vendors on project scope, and forecasting and invoicing as agreed with customer.
Study Start‑up
Co‑ordinate the feasibility planning & selection process of all centres.
Manage And Coordinate The Establishment Of Study Centers Through
Ensuring each center has the necessary trial materials.
Study Close‑out
Work with the clinical team to ensure timely & successful completion of trial. Coordinate the study closeout visits.
Ensure final reconciliation of clinical supplies and ensure that all clinical supplies’ documentation is complete for the study.
Coordinate the final archiving of study related documents.
Financial and Contractual
Analyse monthly financial reports for all allocated projects to identify trends and reasons behind figures, and elevate as required.
Understand all aspects of project finance responsibilities and follow appropriate escalation pathways.
Maintain project utilisation, revenue forecast and recognise identify and implement strategies for improvement (if required) and elevate any significant concerns to management.
Maintain gross margin across allocated projects to meet organisational goals.
Review forecasts for all allocated projects in consultation with each allocated project lead, as needed, during month‑end billing and Project Finance Analyst meetings at least every quarter and develop contingency plans to address any project slippage.
About You
Bachelor’s or Masters degree in a science or related field.
Previous experience working on clinical projects within an academic, CRO or pharmaceutical company environment.
Experience in Oncology is mandatory.
Relevant work experience recommended for this role includes approximately seven (7) years of industry experience. A minimum of two (2) years of Project Management experience within the CRO industry is mandatory. Prior experience as a CRA, in site management, trial coordination, or other relevant industry experience is preferred.
Experience managing single or different regions, working across different therapeutic indications, managing full‑service studies, worked across early phase to Late phases of clinical trial, is preference.
Excellent working knowledge of, and ability to implement project activities in accordance with, ICH/GCP and all applicable regulations and guidelines in the relevant regions.
Previous exposure to client‑facing interactions and/or client management.
Project Finance Management Experience, CRO Preferred
This is a required qualification for the role.
Why Join Us?
At our core,
Emerald Clinical Trials
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 Out
Purpose‑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.
What We Offer
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 programmes, and team‑building events.
Global Opportunities: Be part of a company with international reach, offering you exposure to diverse projects and clients. xcfaprz
We are an equal‑opportunity employer and encourage applications from all qualified candidates.
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Sprachkenntnisse
- English
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