דרושים Director Evaluation & Validation Mcicc ב-Msd ב-China, Huairou District

Job Description

Position Objective

Duties and Responsibilities

• Identify innovative assets from academic institutes, research centers and industry.
• Participate in external project evaluation, collect and analyze information on specific topics related to project of interest to support evaluation, and responding to special due diligence request.
• Write formal reports and prepare presentation materials, such as project evaluation reports, project progress update reports, due diligence reports, data summary presentation, project update presentation etc.
• Generate knowledge graph for disease-indication-therapeutic target
• Analyze scientific literatures on disease and target MOA and related preclinical and clinical data, generate insights on unmet medical needs, critical challenges, emerging development trends, key benchmarks for new drug development, etc.
• Conduct primary research due diligence on indications / targets / technologies of interest, conduct deep dive comparisons on current and emerging treatment options, and identify pipelines to be prioritized as benchmarks, and write comprehensive research reports.
• Monitor scientific and industry progress and update the reports with newly emerging insights periodically.

Key Requirement

Education and background:M.D. in Medicine or Ph.D. in Biology

3-8 years of work experience in assets evaluation, literature research or competitive intelligence of pharmaceutical R&D. Medical training preferred. Previous roles in biotech-focused consulting, biotech equity research, biotech investment analyst with experience in asset-level scientific diligence preferred.

Skills:

• Knowledge of innovations/assets in academic and translational research center
• Strong information search & collection capability, proficient skills in using commercial & public database and various other sources.
• Sharp analytical skills in dissecting preclinical and clinical data with rigorous attention to detail
• Excellent written and verbal communication & presentation skills in Chinese and English.
• High proficiency in writing and formatting reports and presentation, proficient skills in using Microsoft Office tools

Current Contingent Workers apply

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

Job Description

Job Responsibilities:

1- Build and maintain good communication with central government stakeholders including National Healthcare Security Administration (NHSA) and related government agencies.

2- Monitor the timeline, principle and related policy of NRDL adjustment. Enlist key products on NRDL. Drive NRDL listing program as a key coordinator to generate and deliver key value message through cross-department cooperation, and engage different stakeholders including physicians, pharmacists, HE experts.

4- Initiate, design, and carry out projects of reimbursement policy research with associations. Communicate our recommendation on value to government through these projects. Utilize the outcomes to support business strategy.

Job Requirements:

1- Solid work experience in the healthcare industry, at least 8 years of experience in market access

2- Extensive experience in NRDL adjustment.

3- Strong policy sensitivity and strategic thinking.

4- Fluent in speaking and writing English.

5- Proven proficiency in Microsoft Office, including Excel, Word, PowerPoint, etc.

6- Be professional skills in oral and written English.

Current Contingent Workers apply

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

Job Description

The Associate Director, PV is responsible for adverse event management including aggregate and individual case safety report (ICSR) health authority submissions and compliance monitoring.

The Associate Director, PV is also responsible for other activities (as delegated by the PV Lead) which may include but are not limited to: management and negotiation of local PV agreements, local due diligence activities, participation in audits and inspections and related readiness activities, review of local initiatives for compliance with PV requirements, SOP management, local training, communication of safety issues, people development, special projects as assigned, and is able to work on these delegated activities independently.

The PV Associate Director may serve as the Back-up (BU) Local PV Contact / BU Local Responsible PV person as required per local PV legislation. In the absence of the PV Lead, they manage day-to-day PV activities and serve as their back-up.

The primary activities include and not limited to:

1)Serves as the point of contact for the local Health Authority for PV related questions when assigned by the PV Lead and in their absence.

2)If serving as the Local Responsible PV Person Backup, complies with all requirements mentioned in the local laws and regulations.

3) May be responsible for management of one or more direct reports includingecruitment, training, development, and performance management as applicable.

5) May coordinate translation of PV documents and ensure a QC check is performed by a second person for any in-house translations (as applicable).

6)Serves as a SME and supports local PV audits and inspections including readiness activities and supports other audits/inspections including the development of CAPAs in response tofindings/observations.

7) Responsible for reporting adverse experiences or events (AE) or product quality complaints (PQCs) associated with the use of our company products in compliance with Corporate Policy 01: Patient Safety.

8)Participates in and supports audits of contractual partners/vendors as necessary.

10) Develops and maintains local procedures (in compliance with regional and global standards), to ensure global quality PV data and evaluates processes for potential improvement in efficiency and effectiveness.

11)Supports PV Lead in maintaining the local PV Training matrix and onboarding plans as assigned. 12)Supports the development and maintenance of local PV controlled documents (e.g.,

13)Conducts and/or supports PV self-inspections as required by PV Legislations (where applicable). 14)Proactively identifies procedural gaps and challenges and implements solutions in collaboration with all affected stakeholders.

15)Responsible for completing all required/applicable trainings assigned at time of hire and after hire by the due dates, before performing the activity.

17)Responsible for managing and performing local literature screening and assessment in accordance with company procedure and local requirements (as applicable).

18) May be responsible for Health Authority Website Monitoring for potential safety issues, safety alerts, and new/revised PV requirements in compliance with company procedures and local legislation (as applicable).

19)May be assigned responsibility for ensuring appropriate PV language is included in country PV agreements, liaising with business partners, vendors and Alliance Managers as required, performing local qualification/due diligence activities, compliance reviews, and ensuring maintenance of the business partner data tracking system.

21) May be responsible for reviewing, providing input and approving local initiatives (e.g., digital interfaces, marketing initiatives/ patient programs, organized data collection systems, etc.), and other programs to ensure compliance with PV requirements, as applicable.

23)As assigned by PV Lead, responsible for ensuring appropriate implementation and oversight of Risk Minimization Measures, and Additional Risk Minimization Measures locally as per department policy and ensures compliance with local legislations.

24)As assigned by PV Lead,prepare/maintain/submitlocal RMPs to the local HA (as applicable).

25) May participate in PV engagement in relevant externalassociations/industryforums, and regulatory authorities, as applicable

27)Ensures the filing, storage and archiving of safety-related documentation in accordance with company’s policies and local requirements.

33) May participate on special projects or rotational assignments within or outside of China PV as part of their professional development.

Current Contingent Workers apply

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

Job Description

Duties and Responsibilities

• Write formal reports and prepare presentation materials, such as project evaluation reports, project progress update reports, due diligence reports, data summary presentation, project update presentation etc.
• Collect and summarize preclinical and clinical data from various sources for comprehensive landscape mapping of indications, drug targets, and new modalities / technologies, conduct deep dive comparisons on current and emerging treatment options and compose research reports.
• Analyze scientific literatures on disease and target MOA, generate insights on unmet medical needs, critical challenges, emerging development trends, key benchmarks for new drug development, etc.
• Perform in-depth research on emerging technologies and platforms related to RNA, identify significant scientific advancements and trends, and establish prioritized strategies for the development of RNA-related therapeutics.
• Monitor scientific and industry progress and update reports with newly emerging insights periodically.
• Participate in external project evaluation, collect and analyze information on specific topics related to project of interest to support evaluation, and responding to special due diligence request.

Key Requirement

Education and background:Ph.D. / Postdoc in biology with a specialization in RNA-related studies is required. Hand-on experience in RNA biology-related assays.

1-3 years of work experience in one of the following areas: 1) market research or competitive intelligence of pharmaceutical R&D OR 2) academic research or drug R&D focused on RNA biology or RNA structure. Previous positions that involved asset-level scientific diligence (such as roles in biotech-focused consulting, biotech equity research, biotech investment analyst or pharmaceutical pipeline strategy) are preferred but not required.

Skills: Proficient in managing and analyzing substantial volumes of data and able to compile and write reports and presentations in a fast-paced environment

• Strong information search & collection capability, proficient skills in using commercial & public database and various other sources.
• Sharp analytical skills in dissecting preclinical and clinical data with rigorous attention to detail
• Excellent written and verbal communication & presentation skills in Chinese and English.

Current Contingent Workers apply

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

Job Description

• A. Position Objective

• We are looking for a highly motivated individual with expertise in drug design, synthesis, as well as small molecule drug development and evaluation. The overall role is to work on small molecule drug evaluation and validation, and work closely with biologists in the team for assay development and experimental design.

  B. Duties and Responsibilities
• Utilize expertise in drug synthesis and small molecule drug development to lead the initial assessment and screening of small molecule projects, identifying those with the potential for further evaluation and development.
• Conduct in-depth analysis of molecule structures, synthetic routes, and compound properties, integrating molecular and functional group assessments to ensure comprehensive and reliable drug evaluation, and monitor project progress for developmental efficiency.
• Provide critical insights to guide decision-making on potential collaborations, leveraging expertise in small molecule projects.
• Drive and oversee the execution of small molecule project milestones, ensuring coordinated data verification, quality control, and strategic guidance to support innovative collaborations with partners and advance project goals.
• Offer strategic recommendations for optimizing small molecule compound structures, physicochemical properties, and synthesis routes, contributing to the enhancement of project efficiency and success.
• Collaborate closely with the biology team to develop assays and experimental designs, facilitating an integrated approach to small molecule drug evaluation.
• Develop and expand capabilities in the evaluation and collaboration of RNA and peptide-based drug projects, contributing to the exploration of innovative and potential high-impact projects.

Current Contingent Workers apply

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

Job Description

JOB DESCRIPTION – Technology platform evaluation

Job Title: Manager / Senior Manager

Position Objective

Duties and Responsibilities

• Write formal reports and prepare presentation materials, such as project evaluation reports, project progress update reports, due diligence reports, data summary presentation, project update presentation etc.
• Collect and summarize preclinical and clinical data from various sources for comprehensive landscape mapping of indications, drug targets, and new modalities / technologies, conduct deep dive comparisons on current and emerging treatment options and compose research reports.
• Analyze scientific literatures on disease and target MOA, generate insights on unmet medical needs, critical challenges, emerging development trends, key benchmarks for new drug development, etc.
• Perform in-depth research on emerging technologies and platforms related to RNA, identify significant scientific advancements and trends, and establish prioritized strategies for the development of RNA-related therapeutics.
• Monitor scientific and industry progress and update reports with newly emerging insights periodically.
• Participate in external project evaluation, collect and analyze information on specific topics related to project of interest to support evaluation, and responding to special due diligence request.

Key Requirement

Education and background:Ph.D. / Postdoc in biology with a specialization in RNA-related studies is required. Hand-on experience in RNA biology-related assays.

1-3 years of work experience in one of the following areas: 1) market research or competitive intelligence of pharmaceutical R&D OR 2) academic research or drug R&D focused on RNA biology or RNA structure. Previous positions that involved asset-level scientific diligence (such as roles in biotech-focused consulting, biotech equity research, biotech investment analyst or pharmaceutical pipeline strategy) are preferred but not required.

Skills: Proficient in managing and analyzing substantial volumes of data and able to compile and write reports and presentations in a fast-paced environment

• Strong information search & collection capability, proficient skills in using commercial & public database and various other sources.
• Sharp analytical skills in dissecting preclinical and clinical data with rigorous attention to detail
• Excellent written and verbal communication & presentation skills in Chinese and English.

Current Contingent Workers apply

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.