Associate Director, Drug Development
1 week ago
Job Overview Manages professional level employees across multiple levels.; Advice on the development of optimum strategies for drug development, product lifecycle management and portfolio management to meet pharmaceutical and biotechnology customer goals (such as strategic leadership of clinical development plans, go/no go decisions, in-licensing, out-licensing, accelerated time to market, etc).; Provide medical, clinical, scientific, regulatory, and product development consultancy expertise to support strategic business activities and investment opportunities.; Participate in the implementation of mission, goals and objectives, development of policies, procedures and standards for the department.; Provide expertise in pharmaceutical product development by preparing publications, white papers, and blogs in areas of expertise and by participating in scientific conferences and webinars, as appropriate. Essential Functions - Evaluate and develop product development strategies for pharmaceutical products (drugs, biologics, advanced therapies) focusing on clinical-commercial convergence that encompasses all phases of development from discovery to market, including preclinical strategy, clinical strategy, regulatory strategy, and commercial strategy. - Support engagements with regulatory authorities (e.g., FDA, EMA) on behalf of customers, across the lifecycle of drug development from pre-clinical to licensing, including contribution to briefing documents and other meeting materials, and attendance and contribution to meetings and other interactions. - Develop regulatory submissions, including INDs, marketing/licencing authorisations (NDA/BLA/MAAs), special designations (orphan drugs, pediatics plans, “fast-track”, “break-through” etc ). - Ensure high-quality, well-reasoned, objective deliverables (using data-driven design, where available and appropriate) that meet the highest standards of medical, ethical and scientific integrity and conduct. - Provide drug development expertise to support strategic business activities and investment opportunities. - Ensure Customer Satisfaction by working closely with Senior Management, CRO Operations, Therapeutic Units, and other Operations Heads to ensure optimum strategic consultancy to customers. - Serve as a key resource and participate in strategic business development activities including presentations to prospective clients, professional meetings or other business development activities for IQVIA Strategic Drug Development. - Provide internal and external therapeutic and pharmaceutical development-related educational services in support of all branches of IQVIA business. - Attend key scientific meetings/conferences and keep abreast of relevant scientific publications to maintain awareness of current scientific developments and progress in drug development methodology - As appropriate, represent IQVIA or the partner in such meetings. - Compliance with all business office requirements for tracking of time and effort. **Qualifications**: - Typically requires 8 + years of professional experience. - Possesses deep knowledge of one or more related job areas typically obtained through advanced education combined with experience. Typically viewed as having a specialist within discipline. Utilizes expert knowledge to innovate and ensure best practices are applied in all related project work. - Expertise in Excel and PowerPoint. - Strong strategic thinking, analytical and communication skills and ability to thrive in a culture of achievement. - Client-focused and consultative approach for project management - not just an order taker, but is able to suggest alternate approaches and provide strategic insights that meet client needs. - Demonstrates a strong command of a variety of analytical and market research techniques. - Sought out by clients (internal and external) as an analytical expert and, more importantly, as a strategic advisor. - Grasps key issues quickly, understands the "big picture", and links market research insights to larger business issues relevant to client needs. - Demonstrates excellent written and verbal communication skills and is effective in a variety of presentation settings. - Has a strong commitment to quality. - Has a proven track record of meeting or exceeding goals. - Has strong people management skills. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at
-
Associate Director Regulatory Affairs
2 days ago
Singapore Barrington James Full timeAn 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...
-
Associate Director Regulatory Affairs
2 days ago
Singapore Barrington James Full timeAn 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...
-
Associate Director
7 hours ago
Singapore Hummingbird Bioscience Full time $120,000 - $200,000 per yearAssociate Director / Director, Regulatory Science - Hummingbird BioscienceFull-time position –SG based locationABOUT HUMMINGBIRD BIOSCIENCEHummingbird 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...
-
Associate Director
7 hours ago
Singapore, Hummingbird Bioscience Pte. Ltd Full time $120,000 - $180,000 per yearAssociate Director / Director, Regulatory Science - Hummingbird BioscienceABOUT HUMMINGBIRD BIOSCIENCEHummingbird 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...
-
Senior Specialist, Drug Safety
3 days ago
Singapore Organon Full time**The Position** The Senior Drug Safety Specialist is responsible for all assigned pharmacovigilance activities and may serve as the point of contact with local stakeholders, headquarters and the local health authority. Reporting to the Associate Director Drug Safety based in Melbourne, Australia, the Senior Drug Safety Specialist collaborates with...
-
Associate Director
1 week ago
Singapore Hummingbird Bioscience Pte. Ltd Full timeOverview 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....
-
Deputy Director
1 week ago
Singapore A*STAR - Agency for Science, Technology and Research Full timeDeputy Director - AI-driven Drug Discovery (AIDD)Overview: The AI-driven Drug Discovery (AIDD) programme , a national initiative funded by the National Research Foundation and hosted by A*STAR, is seeking a Deputy Director to help lead its mission to transform drug discovery through AI and data science. This role is ideal for a mid-career professional with a...
-
Regulatory Affairs Associate Director
3 days ago
Singapore Ethos BeathChapman Full time**Job Details**: **Location** Singapore **Salary** Competitive Salary **Job Type** Permanent **Ref** BH-178593 **Contact** Piers Atkinson- **Posted** about 1 hour ago - A new entrant to Asia, this Biopharma is looking for a Regulatory Affairs Associate Director. - You will be in charge of all things regulatory in APAC where currently they don’t...
-
Singapore TG SERVICES PTE. LTD. Full time**Leadership and Strategy**: - Lead and manage the drug target identification and validation team, developing strategies to discover and prioritize novel targets for therapeutic intervention. - Provide scientific leadership to integrate target discovery approaches such as genomic, transcriptomic, proteomic, and functional biology studies. - Collaborate with...
-
Scientific Manager
23 hours ago
Singapore ENGAGE GROUP PTE. LTD. Full time**SCIENTIFIC MANAGER - Research & Development / Drug Discovery - Oncology** **The opportunity**: As a Scientific Manager you will lead and coordinate research and development projects in the life sciences sector and contributing to the research and development of latest drugs in oncology. You will have the opportunity to manage a team of scientists,...