Clinical Trial Specialist - French Speaking

At Emerald Clinical Trials, 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 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. About the Role The Clinical Trial Specialist (CTS) is a member of the Clinical Operations team responsible for supporting clinical trial activities as the in-house site start-up and maintenance specialist. As part of the clinical trial project team, the CTS is responsible for ensuring clinical trials are conducted according to Federal Regulations, ICH guidelines, appropriate project plans, IRB/Ethic Committee requirements, and applicable SOPs and guidelines. The CTS works closely with project team to help manage clinical trial feasibility processes, coordinate clinical trial start-up activities including collection of essential documents for site initiation/startup, submissions to central IRBs/Ethic Committees, supporting site staff in the submission to local IRBs/Ethic Committees and changes to Informed Consent Forms (ICFs). Your Responsibilities Increase proficiency in Trial Master File (TMF) set-up and maintenance (filing), both hard copy and electronic as assigned by project . Increase proficiency in uploading and maintaining TMF files and folders in George Clinical’s file-sharing system by project as assigned Serve as second reviewer for TMF QC . May function in the TMF Lead Role and assume responsibility for TMF setup, maintenance and oversight. Assist with/complete end of study TMF filing (including site close out documents), QC and archival. Further develop skills in preparing and participating in audit responses. Perform QC of work (documents, emails etc.) prior to sending out to ensure quality product deliverables . Further develop skills and knowledge of data entry and maintaining files/folders for Clinical Trial Management System by project as assigned. Further develop skills and knowledge of assisting with data entry support, tracking and submission for investigator payments by project as assigned. Works with CRA/CTM/PM during site start-up for feasibility, serving as point of contact for sites where applicable . Assist with presenting final feasibility results to PM team and/or Sponsor. Assists the sites in preparation, planning, organizing and collecting essential document packets (EDPs). Submit final EDPs to sponsor or CTM/PM as required . About You College / University diploma / degree; OR at least 2 years related experiences and / or training; OR equivalent combination of education and experience . Ability to perform general administrative duties as needed or required . Exposure to medical terminology preferred. Knowledge of ICH/GCP, ethical and regulatory requirements preferred Must be fluent in French & English What We Offer We 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. We are an equal-opportunity employer and encourage applications from all qualified candidates. The expected salary range for this position is $60,000 - $90,000 per year, depending on experience and qualifications. This range is in USD and there may be an adjustment for salaries in Canada.

The Clinical Trial Specialist supports in-house site start-up and maintenance activities while ensuring compliance with federal regulations and ICH/GCP guidelines. Responsibilities include managing Trial Master File (TMF) documentation, assisting with feasibility processes, and coordinating submissions to IRBs and Ethics Committees.

Candidates must hold a college or university diploma or degree, or possess at least two years of relevant experience. Fluency in both French and English is mandatory, along with a strong understanding of clinical trial regulatory requirements.

• Competitive compensation • Hybrid or remote working arrangements • Career growth opportunities • Employee wellbeing programs • Recognition programs

• Regulatory CompliancePreferred
• Administrative SupportPreferred
• Quality ControlPreferred
• Data entryPreferred

Identified from the job description. Confirm important requirements above.

• Clinical trial management
• Trial master file maintenance
• Site start-up
• Regulatory compliance
• ICH guidelines
• GCP knowledge
• Data entry
• Administrative support
• Medical terminology
• French language proficiency
• English language proficiency
• Feasibility assessment
• Quality control
• IRB submission
• Informed consent forms
• Informed Consent
• Engagement Surveys
• Ethical Standards And Conduct
• Administrative Functions
• Medical Devices
• Planning
• Research
• Auditing
• Biopharmaceuticals
• Clinical Research
• Clinical Trials
• Clinical Trial Management Systems
• Data Entry
• English Language
• French Language
• Marketing
• Good Clinical Practices (GCP)
• Innovation
• Oncology
• Medical Terminology
• Operational Excellence
• Operations
• Relationship Building
• Team Building
• Trial Master File
• Filing
• ICH Guidelines
• Institutional Review Board (IRB)

• Healthcare
• Science & Research
• Administrative
• Clinical Trial Specialist
• Clinical Research Associate
• Biologists, Botanists, Zoologists and Related Professionals
• Clinical Research Coordinators
• Natural Sciences Managers

Minimum education

Bachelor’s degree

Minimum experience

0+ years

Posting language

English

Working hours

40 hours per week

Location requirements

Country, Singapore