Global Study Start-Up Submissions Lead

1 week ago


Singapore Medpace Full time

An established industry player is seeking a dedicated Study Start Up Submissions Manager to enhance their Clinical Operations team in Singapore. In this full-time role, you will oversee the global start-up process, ensuring all submissions are accurate and compliant. Your expertise in clinical research and project management will be crucial as you navigate challenges and present solutions during key meetings and audits. Join a forward-thinking organization where your contributions will directly impact clinical trials and patient care. If you are passionate about clinical research and thrive in a dynamic environment, this opportunity is perfect for you. #J-18808-Ljbffr



  • Singapore Medpace, Inc. Full time

    Job Summary: We are currently seeking a full-time, office-based Study Start up Submissions Coordinator to join our Clinical Operations team in the Singapore office. This role is a vital part of the team to accomplish tasks and projects that are instrumental to the company’s success. If you are interested in an exciting career where you can use your...


  • Singapore Novartis Farmacéutica Full time

    Choose LocationChoose Location# SSO Study Start-up ManagerREQ- Nov 09, 2025Singapore### Summary#LI-Hybrid Location: Singapore About the Role: The SSO Study Start-Up Manager is accountable for study planning, SSU activities and activation deliverables of assigned projects in compliance with Novartis processes, GCP/ICH and regulatory requirements in a...


  • Singapore Precision for Medicine Full time

    Precision for Medicine is a Clinical Research Organization. Precision's uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition...


  • Singapore Premier Research Full time

    Premier Research helps highly innovative biotech and specialty pharma companies transform life-changing ideas into reality. We have positioned ourselves right in the middle of the action, targeting unmet needs in Rare Disease and Pediatrics, Analgesia, Neuroscience, Oncology, Dermatology, and Medical Devices. We're looking for a talented and energetic...

  • Clinical Lead

    1 week ago


    Singapore Novotech Asia Full time

    This position is open to all APAC countries including AU and NZ. **Brief Position Description**: The Clinical Lead (CL) and Senior Clinical Lead provides direction and guidance to multi-country clinical teams in assigned project(s), coordinates site management and monitoring activities, and provides operational leadership for clinical teams to achieve...


  • Singapore IQVIA Full time

    **Responsibilities**: - Ownership of country and site budgets. Development, negotiation and completion of Clinical Trial Research Agreements (CTRA). - Oversees and tracks clinical research-related payments. Payment reconciliation at study close-out. Oversees FCPA, DPS/OFAC, and maintenance of financial systems. Financial forecasting in conjunction with SCOM...


  • Singapore PHARMACEUTICAL RESEARCH ASSOCIATES SINGAPORE PTE. LTD. Full time

    ICON is offering an opportunity to work within our dedicated, talented, supportive and friendly Global Regulatory Clinical Services (GRCS) team in clinical trials. The GRCS team has been in operation for 25+ years and comprises more than 400 regulatory professionals located in 48 countries, managing submissions in 60+ countries. As part of the GRCS team,...


  • Singapore Cognizant Full time

    A leading consulting firm in Singapore is seeking a Regulatory Affairs professional to handle global regulatory submissions and maintain documentation. This role requires 1 to 3 years of experience in the pharmaceutical or medical device industry, with strong documentation skills and stakeholder interaction capabilities. The position offers a dynamic working...


  • Singapore Temasek Polytechnic Full time

    **What the role is** - Lecturer / Centre for Transcultural Studies in the International Relations Department. **RESPONSIBILITIES** - Teach, facilitate tutorials and monitor students’ learning - Supervise and develop students through activities, projects or competitions - Participate actively to poly-wide/department events or activities - Engage overseas...

  • Compliance Lead

    1 week ago


    Singapore TENTEN Partners Pte. Ltd. Full time

    **My client is a fast-growing start-up revolutionizing the securities trading platform. We seek a motivated Compliance Lead to build and oversee our compliance framework from scratch.** **Responsibilities**: - Develop and implement a comprehensive compliance program. - Establish policies, procedures, and controls to ensure regulatory compliance. - Conduct...