Associate Director

2 days ago


Singapore Hummingbird Bioscience Pte. Ltd Full time

Overview Associate Director / Director, Regulatory Science - Hummingbird Bioscience Full-time position – SG based location About Hummingbird Bioscience Hummingbird Bioscience is a biotherapeutics company working at the interface of artificial intelligence and human innovation to discover and develop transformative medicines for hard-to-treat diseases. Hummingbird Bioscience’s computational and systems biology technologies have generated a pipeline of innovative clinical-stage monoclonal antibodies and antibody-drug conjugates in oncology and autoimmunity. At Hummingbird Bioscience, the commitment to rigorous science, teamwork, and intellectual integrity underpins our passion to accelerate the journey of new drugs from concept to clinic. For more information, please visit and follow Hummingbird Bioscience on LinkedIn, X (formerly Twitter), and YouTube. About the Role The Regulatory Science, Associate Director / Director will serve as a key member of the Regulatory Science team at Hummingbird Bioscience. This role will be responsible for developing and executing global regulatory strategies and ensuring timely preparation and submission to support clinical trials and regulatory interactions worldwide. This is a technical, individual contributor role with cross-functional impact, working closely with development teams, external partners. The successful candidate will guide regulatory decision-making across development stages and contribute to both Clinical and CMC regulatory activities for a growing oncology pipeline. Responsibilities Oversee Clinical Trial Submissions: Coordinate and oversee the preparation of clinical trial applications across multiple regions, including the United States and Asia-Pacific. Ensure that all submissions are timely, complete, and meet relevant regulatory requirements. Support the preparation, and submission of applications for regulatory designations (e.g., Fast Track, Breakthrough Therapy, Orphan Drug etc.) Hands-On Implementation: Actively engage in the drafting, reviewing, and coordination of regulatory documents, ensuring accuracy and timeliness. This role requires both strategic oversight and a willingness to be directly involved in execution. Lifecycle Maintenance of Submissions: Manage post-submission activities including regulatory amendments, protocol and investigator brochure updates, and general IND/CTA maintenance across regions. Vendor Oversight: Manage regulatory vendors (e.g., CROs, publishers, consultants), ensuring deliverables are of high quality, aligned with internal expectations, and meet timelines. Adaptability and Problem-Solving: Operate effectively within a dynamic startup environment where roles and priorities may evolve. Be prepared to handle emerging challenges and adjust plans as necessary. Cross-Functional Collaboration: Work closely with internal teams—including clinical operations, medical, safety, CMC, and nonclinical—to align regulatory activities with program goals and timelines. Ensure consistent communication across functions to support submission readiness. Qualifications Educational Background: Bachelor’s degree in a relevant scientific or regulatory field is required; a Master’s degree is preferred. Experience: Minimum of 7 years of experience in regulatory science, clinical trial submissions, or related roles, with demonstrated progression in responsibility. Communication: Strong written communication and presentation skills, including the ability to independently prepare clear, well-structured regulatory slides for cross-functional discussions. Regional Experience: Experience in dealing with regulatory submissions in the US and Asia-Pacific region is highly desirable. Experience with oncology trials is highly desirable. Prior experience with NMPA submissions is a plus. Flexible and Adaptive Mindset: Ability to thrive in an environment where processes are evolving and to adapt to shifting priorities. Hands-On Approach: A readiness to engage directly with operational tasks and ensure that strategic plans are executed effectively. Our Mission & Values Our fast-growing biotechnology company is committed to discovering and developing important new drugs for cancer and autoimmune diseases, and living by our values: Excellence, Determination, Teamwork, Intellectual Integrity and Audacity. Join Us at the Frontier of Drug Discovery and Development We are looking for passionate and motivated individuals committed to solving important, complex problems. We are committed to the personal and professional development of our team and offer robust learning and development programs. Hummingbird Bioscience understands the need for flexibility for our team and offers a generous paid time off program with flexibility to support employees through different life stages. We invest in our team’s health by offering competitive benefits including health and dental insurance, and a comprehensive and holistic employee assistance program. We foster a more collaborative, productive, and sociable culture with on-site lunches and snacks. Finally, we believe in creating social impact beyond our business through corporate social responsibility initiatives. Are you ready to join us on our mission to discover and develop important new drugs for cancer and autoimmune disease? Click on ‘Apply for this Job’ to submit your application. For enquiries, please email us at Hummingbird Bioscience is firmly committed to Equal Employment Opportunity (EEO) and to compliance with all Singapore and US federal, state and local laws and/or guidelines that prohibit employment discrimination on the basis of age, race, color, gender, sexual orientation, gender identity, ethnicity, national origin, citizenship, religion, genetic carrier status, disability, pregnancy, childbirth or related medical conditions, marital status, protected veteran status and other protected classifications. #J-18808-Ljbffr


  • Associate Director

    4 days ago


    Singapore APCO WORLDWIDE ADVISORY SERVICES PTE. LIMITED Full time

    **Job Description & Requirements**: Founded in 1984, APCO Worldwide is an award-winning, independently owned global communication and business strategy firm with offices in major cities throughout North America, Europe, the Middle East and Asia. APCO combines a global perspective with local expertise to help clients around the world manage challenges,...

  • Associates Director

    2 days ago


    Singapore SIGNIUM INTERNATIONAL PTE. LTD. Full time

    SIGNIUM is a global partnership in executive search and leadership consulting which offer three core solutions: - Executive Talent Acquisition - Leadership Consulting and Development - Assessment and Succession Planning At SIGNIUM, we grasp every opportunity to surprise others and ourselves by going beyond expectations to deliver the extra. We call it...

  • Associate Director

    1 week ago


    Singapore Waystone Full time $1,500,000 - $2,000,000 per year

    Waystone leads the way in specialist services for the asset management industry.Partnering with institutional investors, investment funds and asset managers, Waystone builds, supports and protects investment structures and strategies worldwide.With over 20 years' experience and a comprehensive range of specialist services to its name, Waystone is now serving...


  • Singapore Adsan Law LLC Full time

    Join Our Dynamic Team as Associate Director!Adsan Law is looking to expand its practice capabilities in the following practice areas: Information Technology & Intellectual Property Family & Private Clients Litigation, Arbitration & Dispute Resolution We are seeking driven individuals to join us as Associate Directors. This is an exceptional opportunity to...


  • Singapore Fervent Chambers LLC Full time

    Overview Fervent Chambers LLC is dedicated to advancing our clients' causes with passion and expertise. Specializing in corporate and commercial work, we handle major cross-border disputes involving complex legal points and intricate facts. Our firm has extensive experience in the fields of shipping, oil and gas, engineering, construction, and infrastructure...


  • Singapore Hays Full time

    Investment, Associate Director My client is an Endowment Fund, located in Singapore. They are looking for an Investment Associate Director to join their investment team. **Investment, Associate Director** My client is an Endowment Fund, located in Singapore. They are looking for an Investment Associate Director to join their investment team. **Your New...


  • Singapore ASPIRE GLOBAL NETWORK PTE. LTD. Full time

    **Associate PR Director Our client are a growing financial PR agency, specialising in Finance, FinTech, Technology and ESG clients and they are seeking an Associate Director to join their Singapore team. As a key member of the leadership team, the Associate Director will be responsible for managing a portfolio of clients and overseeing the development and...

  • Associate Director

    2 weeks ago


    Singapore Cultivar Staffing & Search Full time

    Overview The hiring company is a local brand communication firm assisting thousands of large enterprises in crafting the right brand messages for intended results. Due to expansion, they are looking to fill the role of Associate Director . Responsibilities Growth and development of new accounts and existing accounts Working with Business Development team for...


  • Singapore Barrington James Full time

    An innovative and purpose-driven biotechnology, biologics company is seeking a Regulatory Affairs Associate Director to join its growing team. This role will be instrumental in shaping and executing global regulatory strategies, supporting clinical development across oncology and autoimmune programs. As a senior individual contributor, the Regulatory Affairs...


  • Singapore Barrington James Full time

    An innovative and purpose-driven biotechnology, biologics company is seeking a Regulatory Affairs Associate Director to join its growing team. This role will be instrumental in shaping and executing global regulatory strategies, supporting clinical development across oncology and autoimmune programs. As a senior individual contributor, the Regulatory Affairs...