Providing functional, high-purity recombinant proteins—including membrane proteins and nanodiscs—to overcome bottlenecks in drug screening and target validation.
Harness the power of protein degraders for precise protein degradation, expanding druggable targets and enhancing therapeutic effectiveness for cutting-edge drug discovery.
RNA design, synthesis, and manufacturing—covering mRNA, saRNA, circRNA, and RNAi. Fast turnaround, rigorous QC, and seamless transition from research to GMP production.
Balancing accuracy, accessibility, affordability, and rapid detection to safeguard public health and strengthen global response to infectious diseases.
Stable expression over 15 generations with rapid cell line development in just 3 months. Supports adherent and suspension cell lines, offering MCB, WCB, and PCB establishment.
Scalable mRNA production from milligrams to grams, with personalized process design for sequence optimization, cap selection, and nucleotide modifications, all in one service.
Leverage AI to uncover hidden high-potential small molecules, prioritize leads intelligently, and reduce costly trial-and-error in early drug discovery.
Our promise to you: Guaranteed product quality, expert customer support.
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Project Manager, Nucleic Acid Drug Development
The individual will be a key member of the R&D team. The primary responsibilities are to lead the company's R&D program of nucleic acid drugs, expand and optimize the current technology platforms, and develop long-term scientific, research, and technological plans for the company.
Key Responsibilities:
Provide leadership and scientific directions to individual R&D groups relevant to the discovery phase of nucleic acid drug development.
Oversee the effort to improve current platform technologies.
Develop new technology platforms to strengthen the current nucleic acid drug development and characterization programs.
Design experimental schemes, troubleshoot and optimize experimental protocols, and validate experiment data.
Work with other groups within R&D to track and support projects through each stage of development.
Manage several projects concurrently to meet aggressive product launch timelines.
Represent the company's technology arm to participate in business negotiations and scientific conferences.
Basic Qualifications:
A M.S. or Ph.D. degree in a relevant scientific discipline (e.g. Biological or Chemical Engineering, Biology, Biomedical Sciences) is required.
A minimum of 5 years' experience in nucleic acid drug development.
Prior experience leading a nucleic acid drug development program.
Strong communication and presentation skills.
Comprehensive knowledge of all aspects of nucleic acid drug development, from target identification, drug development, assay development, candidate screening, and downstream process development.
Comprehensive knowledge of recombinant expression technology, including construct design, cell culture, fermentation, and purification in both prokaryotic and eukaryotic systems.
Ability to adapt quickly to a market-oriented R&D operation.
Must be adaptable and flexible to meet changing priorities.
Creative Biogene is an equal opportunity employer and does not discriminate against otherwise qualified applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or handicap, or veteran status.