Job Postings
We are looking for talented, skilled, science-focused individuals who want the opportunity to work with top scientists, build valuable relationships, contribute to high-performing teams, and grow with us as we continue to forge a new path to fight cancer and improve the lives of patients.
Come learn with us, grow your career, and make significant contributions as we work to improve the lives of people with cancer through the development of precisely-targeted medicines with differentiated mechanisms of action.
If you are interested, please submit your resume to HR@angelpharma.com
Process Chemist
Responsibilities:
1． According to the target of the project, consult relevant literature, develop the process research and development plan;
2． Design and implement experiments according to process development plan;
3． Process development includes but is not limited to: reaction condition optimization, impurity preparation and separation, post-treatment condition optimization, separation and purification, and crystallization process development and research;
4． Clear and standardized completion of experimental records;
5． Collect, analyze, summarize and report related data;
6． Participate in project outsourcing affairs contact and follow up;
7． Assist to maintain the normal operation of experimental instruments and ensure the safety of experimental environment.
Qualifications:
1． Bachelor degree or above in organic chemistry or pharmaceutical chemistry, at least 1 years related working experience is required.
2． Good organic synthesis skills and good laboratory safety awareness;
3． Meticulous experiment operation, strong data collection and analysis ability;
4． Rigorous and practical, strong sense of responsibility, good at communication, team spirit, can independently carry out conventional organic chemical process research and development;
5． Good literature review and interpretation skills;
6． Good learning ability;
7． Good English reading and writing skills;
8． Experience in organic chemical process projects is preferred.
Clinical Pharmacology Director/Manager
Responsibilities:
1. Serve as a program level clinical pharmacology lead and a PK/PD content expert and has a broad range of responsibilities that include developing and prioritizing strategic, tactical, and participation in multiple matrixed research and development teams.
2. Contribute to early development and clin pharm strategy, as well as the planning and implementation the appropriateness of study designs, and generate high quality of data, adherence to Good Clinical Practices to meet both domestic and international requirements.
3. Contribute to the preparation of submission documents to health authorities.
4. Work with cross-functional team to establish project success criteria, monitoring project progress, and communicating information to management.
5. Ensuring that clinical pharmacology requirements are understood and incorporated upfront from product concept development. This helps ensure that products are developed in a way that will facilitate prompt regulatory approvals with competitive advantages in the intended markets.
6. Participate in assessing new product opportunities and identifying requirements for projects under consideration, including evaluation of clinical pharmacology and clinical efficacy data owned by external organizations with regard to potential product acquisitions or partnering in product development.
Qualifications:
1. Ph.D. in Pharmacology or PharmD with a minimum of 5 years of industry experience is required.
2. Prior experience in oncology drug development and interactions with regulatory authorities is preferred.
3. Knowledge in drug metabolism, pharmacokinetics, pharmacodynamics, clinical trial design, and regulatory requirements for drug development is required.
4. The ability to work in a matrix environment with global/local cross-functional teams is essential.
5. Excellent communication skills, self-motivated, innovative, with highest level of professional ethics, accountability.
6. Proficient in English (oral and written).
