HaiHe Recruiting | 我们期待您的加入

＞PhD +/- post doctoral experience in synthetic organic, medicinal chemistry with at least 7 years of directly relevant experience in small molecule drug discovery.

＞Strong proficiency in fundamental aspects of drug discovery and demonstrated ability to advance drug discovery programs are essential.

＞An in-depth understanding of biology, pharmacology, DMPK and ability to integrate these disciplines toward successful project advancement.

＞Strong skills in gathering, documenting, and analyzing information from competitive sources such as patents and meetings and using this information to guide program strategy.

＞Demonstrated strong leadership skills in cross-functional teams, either as project team leader or co-lead.

＞Excellent written and oral communication, interpersonal, and organizational skills.

＞Ph.D. in chemistry or related discipline with a minimum of 3 years industry experience in drug discovery.

＞Successful experience in new drug development from target to final drug candidate compound preferred.

＞Strong background and experience in organic chemistry (methodology, catalysis, total synthesis etc) is required, along with a proven track record of solving complex problems.

＞Good problem solving and interpersonal skills with the ability to work well with members of the research teams in a dynamic and highly collaborative environment.

＞Experience in leading and collaborating with CRO chemistry teams is a plus.

＞Doctoral degree in life sciences with 5+ years of postdoctoral industrial and academic working experiences, or master’s degree with equivalent qualifications.

＞Comprehensive, in-depth knowledge of cancer biology and small molecule drug discovery.

＞Broad in vitro biochemical and cellular assay development experiences.

＞Proven track record of contributions in delivery of milestones and advancing drug discovery projects. 

＞Strong publication record is a plus.

＞Experiences in managing studies at CRO is a plus.

＞Doctoral degree in life sciences with 3+ years of postdoctoral working experiences with a focus on oncology or immuno-oncology; or Master degree with equivalent qualifications.

＞Experiences in exploring the pharmacologic effects and MoA of therapeutic agents, and/or the biological functions of proteins.

＞Strong hands-on skills in molecular and cellular assays is a must, hands-on skills in genetic, epigenetic or immuno-oncology assays is a plus.

＞Demonstrated track record of achievements as shown by strong publications and/or patents.

＞Knowledge in precision medicine and biomarkers is desired.

＞Ability to deliver high quality work in a dynamic, fast-paced environment.

＞Excellent written and oral communication skills in English is a plus.

＞Have experience as in-house patent for more than 3 years.

＞Experience in the pharmaceutical industry and general familiarity with and strong understanding of pharmaceutical R&D, and commercialization.

＞In-depth knowledge and experience in counseling drug discovery and development and commercial launch.Proven track record of patent portfolio development.

＞Excellent drafting, negotiation and communication skills, with the ability and confidence to represent HaiHe in the area of patent law.

＞A demonstrated ability to collaborate, as well as to work independently, balancing competing priorities in a fast-paced environment with a high level of professionalism.

＞Strong analytical and strategic mind-set.

＞Fluent in English is a plus.

＞MS degree in science plus at least 1 years or above experience in analytical chemistry, pharmacokinetics, or metabolism.

＞Familiar with the use of standard laboratory equipment (e.g., balances, pipettes, centrifuges).

＞Experience with use and trouble shooting of analytical equipment such as LCMSMS.

＞Knowledgeable on a variety of study types, analysis procedures and methodologies.

＞Excellent communication skills and interpersonal skills.

＞MS degree in the area of Formulation, Pharmacy, etc; more than 5 years of working experience including innovation, management and hands-on abilities.

＞Expert on formulation and related regulatory. Strong ability for formulation R&D and plant production with teamwork sprite.

＞Excellent communication skills and interpersonal skills.

＞Team management experience is a plus.

＞Minimum 3 years working experience in quality department with good understanding of quality standards and requirements and production processes. Working experience in a GMP environment in pharmaceutical/API industry.

＞Experienced in handling deviations, change control, manufacturing/analytical batch record review.

＞Fast learner with ability to adapt to changes, and with continuous improvement mindset. Able to write and communicate well in English  and in Chinese language.

＞Good knowledge of Process Validation.

＞Medical background, a master degree of clinical medicine in a certain therapeutic area ( Oncology preferred).

＞Familiar with the knowledge of the clinical practice in oncology area,GCP and the SOP of clinical study.

＞7 year experience or more in all aspects of clinical monitoring as well as clinical project management.

＞Ability and experience to complete medical surveillance projects independently.

＞Accurately understand the time required to perform routine medical surveillance tasks, develop appropriate schedules, and provide accurate resource estimates and allocations.

＞Exceptional leadership and executive skills with a team player attitude.

＞Fluent in written and verbal English.

＞At least 3 years and above of relevant experience in medical intelligence and pharmaceutical market analysis.

＞Master's degree or higher in a pharmacy-related field.

＞Proficiency in the use of various scientific/intelligence databases, both domestic and international.

＞Knowledge of drug development related knowledge, clinical development related knowledge.

＞Excellent communication skills and interpersonal skills.

＞Master's degree or higher in a pharmacy-related field.

＞3 years+ experience of medical writing within the pharmaceutical/biotechnological industry/CRO.

＞Good working knowledge of the clinical drug development process with experience in integrating information from all phases of clinical development into clinical-regulatory documents/submissions.

＞Fluent in written English, be able to build up Chinese document based on Global English document shell. Ability to proofread the English version back-translated from Chinese to English.

＞Ability to demonstrate a familiarity with principles of clinical research and to interpret and present clinical data and other complex information.

＞MS/MBA in life science (clinical medicine and pharmacy preferred) and 3+ years relevant clinical trial management experience in pharmaceutical development is required; candidates with Bachelor's degree plus 5+ year of clinical trial management experience will be considered.

＞Good knowledge of ICH Good Clinical Practice, clinical trial design, regulatory processes. Knowledge of Global clinical development process preferred.

＞Basic knowledge of oncology and/or hematology, or experience in early clinical development preferred.

＞Master in the use of project management software application (such as, but not limited to, Microsoft Project) and strong computer skills working with Microsoft Office programs is required.

＞Strong interpersonal skills; ability to interact and communicate professionally with all levels of the organization.

＞Fluent in English and Mandarin, both written and oral.

＞Demonstrated work ethic, integrity and professional conduct.

＞Master/Bachelor’s degree in life science (clinical medicine and pharmacy preferred) and at least 2 years relevant investigational site management experience in pharmaceutical development is required.

＞Good knowledge of ICH Good Clinical Practice, relevant international and local regulations relating to Clinical Research.

＞Basic knowledge of oncology and/or hematology, or experience in early clinical development preferred.

＞Strong interpersonal skills.

＞Demonstrated work ethic, integrity and professional conduct.

＞Fluent in English is a plus.