Responsibilities:

• As a key member of discovery leadership team, design and execute biology strategy to build and deliver a pipeline of high value projects.
• Set-up the US biology lab and perform day-to-day management.
• Recruit and develop talents, build a strong team with deep scientific expertise.
• Design and develop novel and solid biological assays for drug discovery.
• Establish and maintain relationship with external resources, such as research institutes, CROs, and KOLs, to support internal programs.
• Perform due diligence of external opportunities in collaboration with BD and other relevant functions.
• Supports other projects as needed.

Qualifications:

• Ph.D. (biology/life science-related) with >5 years of Industrial experience in pharmaceutical /biotech/CRO industry in Biology/Discovery department.
• Deep experiences in oncology/immunology related biological assay development and animal models.
• Key Experience:
  • Strong experience in molecular biology, biochemistry, and cellular biology.
  • Working knowledge of different therapeutic modalities, including but not limited to small molecule, large molecule, ADC, molecular glue etc.
  • Strong track record of publication in peer reviewed journals or holds high quality patents.
  • Experience of leading drug discovery projects: from Target ID to PCC and/or PCC to IND.
  • Excellent people management skills and capable of building a strong scientific team.

• Responsibilities:

  • Create strategic hospital/ key account plans utilizing detailed understanding of hospital and physician priorities, defining opportunities for assigned brands.
  • Implement key account plans and drive performance of Antengene’s portfolio to achieve sales objectives and key performance indicators for assigned brands.
  • Support access for patients in securing Hospital Formulary Listing of new brands/indications.
  • Utilize in-depth disease/product knowledge to define clinical place for assigned brands that meets needs of customers.
  • Shape positive brand perceptions and create advocacy through clear demonstration of value proposition for physicians and patients.
  • Monitor market landscape and proactively provide regular update on market intelligence including competitor activity, industry trends and healthcare system.
  • Manage resources and expenses effectively with good stewardship within guidelines to effectively implement marketing plan and activities.
  • Recommend viable solutions to capitalize on opportunities in the market and address challenges.
  • Lead implementation of marketing and key account activities, including working with medical affairs to deliver medical education to support quality use of medicines.

   

• Qualifications:

  • Proven record of sales achievement with minimum 5 years in sales or account management in biopharmaceutical industry.
  • Proven ability to identify growth opportunities, address challenges in accounts, developing and executing key account plans to achieve sales forecasts.
  • Familiar with local healthcare system, stakeholder management and hospital listing process.
  • Prior experience/knowledge in Hematology Oncology is an advantage.
  • Strong analytical and problem-solving skills.
  • Autonomous with the ability to work independently.
  • Demonstrate values of:
    • Entrepreneurial Spirit.
    • Passionate to make a difference for our patients.
    • Committed to extending access to innovative medicines.
    • Act with Speed & Integrity to collaborate with stakeholders in commercialization.
    • continually strive towards Standards of Excellence.

Responsibilities:

• Manage global or regional studies and involve in the design, conduct, monitoring, data interpretation and reporting of individual clinical trials.
• Provide expert scientific and clinical input to Clinical Development, Regulatory Affairs, Biostatistics, Data Management, and other related departments.
• As a trial level physician and medical monitor for clinical studies.

Qualifications:

• M.D. degree, 2Y+ industry drug development experience.
• Experience specific to oncology preferred.
• Fluent in English, both verbal and written.

Responsibilities:

• Perform Medical Review of adverse event reports including but not limited to all serious, events of special interest.
• Provide input to key internal safety documents, including Risk Management documents (RMPs), development and updates/maintenance of expectedness guides.
• Provide support for investigator brochures, protocols, informed consents, final study reports, as appropriate.

Qualifications:

• M.D. degree & 5Y+ pharmacovigilance experience in drug development pharma/biotech industry.
• Experience specific to hematology preferred.
• Fluent in English, both verbal and written.

Responsibilities:

• Be responsible for study protocols, CRF, ICF, lab manual, pharmacy manual, clinical monitoring plan.
• Keep closely relationship with site and submissions for ICH-GCP, site contract process and governor approval.
• Contribute to PI and site identification, communications, and initiation.
• Contribute to site feasibility process.

Qualifications:

• Bachelor degree or above in Clinical Medicine/Pharmacy.
• 1Y+ clinical project management, oncology project experience preferred.

International project experience is preferred.

Responsibilities:

• Research, write, and edit clinical documents, including clinical study protocols, clinical study reports, IB, ICF, RMP, clinical plan outlines, and scientific manuscripts.
• Review statistical analysis plans and mock statistical output to assist in determining appropriateness of content/format for clinical writing.
• Provide medical editing review of draft and final documents.
• Perform literature searching and reviews as necessary.

Qualifications:

• Medical related degree & 2Y+ medical writing experience.
• Experience in clinical study design and protocol development and CSR/writing.
• Fluent in English, both verbal and written.

Responsibilities:

• Establish Medical Strategy for pre-launch brand and pipeline products.
• Conduct productive engagement with key national stakeholders.
• Design and compose study protocol post launch.
• Design and implement medical activities.
• Provide strategic advice and support for corporate business development.

Qualifications:

• Master degree or above in Clinical Medicine/Biology.
• 3Y+ medical experience on Hematology/Solid Tumor area.
• Experience of clinical trial design and implementation.

Responsibilities:

• Establish regional KOL list and implement KOL engagement plan, develop our core KOL and build up academic branding.
• Deliver Lasted therapeutic area knowledge and product information to our clients, collect regional insights and identify clinical unmet needs and KOL’s needs.
• Support medical team to follow up Post-Launch clinical trials with high quality and efficiency.
• Execute local and central medical education activities, and train sales and marketing team in terms of brand and therapeutic area.
• Across-Function support: Support sales, marketing, clinical development, and other functions.

Qualifications:

• Master’s degree or above, medical related subjects, clinical background will be a plus.
• At least 1 year working experience of MSL, especially with MNC MSL experience.
• Strong affinity, positive, a good team player, and strong communication skills.
• Previous experience of hematological malignancy or oncology area.
• Fluent read and written English, ability to communicate orally in English will be a plus.

Responsibilities:

• Define the product vision and drive the roadmap for new products.
• Plan and develop brand strategies and initiatives that are in line with the growth drivers and business objectives.
• Internalize and represent the customers’ voice throughout the product lifecycle.
• Collect and measure key product metrics against goals to inform success of each release and plan iterations accordingly.
• Develop critical relationships with national Key Opinion Leaders and other allied health care professionals.
• Set up KOLs communication workshops to understand the patients /physicians’ insights.

Qualifications:

• Bachelor’s degree or above in Clinical Medicine/ Pharmacy or other related major.
• 5+ years’ experience in product management, experience with Oncology products is preferred.
• Good Customer Insight including understanding customer needs, behaviors, motivational drivers.
• Fluent read and written English.

Responsibilities:

• Conduct regular audits and special projects independently according to IA Manual and audit plan.
• Timely complete reports and working papers with sufficient information / evidence obtained.
• Set up regular communication to Management on any risks, findings, and recommended action plans after full alignment with relevant owners.
• Closely follow up on remediation status and results, providing control suggestion wherever needed.
• Fully support on company internal controls improvement.
• Provide proactive supports on compliance monitoring programs.
• Assist on regular AC or CCC (Compliance Committee) meetings preparation.

Qualifications:

• Bachelor’s degree or above, CPA or CIA is a plus.
• 3-5 years of audit or internal control experience in multinational company and is familiar with audit methodologies. Experience in Pharm / healthcare industry is preferred.
• Around 20% of travel (short duration) is required as needed.
• Good verbal and written English and Chinese.
• Have passion in audit work and interest in fast-growing company.
• Good leadership and great team spirit; Ability to interact with multiple BPs in complicated organization.

Responsibilities:

• Establish ATG training system, including training center, training system, training materials, training plan and training delivery.
• Develop yearly training objectives, training plan and manage training budget accordingly to different level targets.
• Define certification standard of all staff at different levels and function.
• Support to global/local staff to develop technical and non-technical training course according to predefined objectives and plan.
• Work closely with supplier on training preparation and implementation to ensure training delivery quality and efficiency.
• Participating and supervising training course delivery.
• Developing and conducting training evaluation to collect trainee feedback on training delivery. Using the result to improve training quality and efficiency, as well as training environment setup.

Qualifications:

• Bachelor and above degree.
• 5+ years’ training experience in pharmaceutical industry.
• Strong analytical background with strategic and user centric thinking capabilities, influencing skills, attention to detail and ability to effectuate change.
• Solid understanding of training strategy.
• Good communication skill and team spirit.
• Fluent English speaking.