Jobs at Msd in Kenya, Nairobi

Job Description

Administrative Support: to manage line manager’s schedules, coordinate appointments and meetings, prioritize incoming requests and deadlines and work on expense claim reports, ensuring timely completion.

Travel Planning:to manage travel documents (incl. VISA, Passport), domestic and inter-continental flights, hotel, ground transportations, ensuring a smooth connection.

Data Management:perform regular data analytic based on Visier or Workday raw data, including generate report, maintain monthly HR dashboard, conduct comparison or analysis, then drive insight.

Confidentiality:often entrusted with sensitive and confidential information, must maintain a high level of confidentiality and exercise discretion when handling such information.

Technology Skills Support:is expected to be proficient in using various software applications, communication tools, and office equipment.

Current Contingent Workers apply

No Travel Required

Not ApplicableNot Indicated

*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

1. HPV female & male team market performance insight generation (primary & secondary data);

2. Annual finance forecasting model;

3. HPV Team key initiatives integration and tracking

4. Annual business planning integration and execution plan integration

5. Management report and dashboard

6. Assessment on pipeline opportunities

Current Contingent Workers apply

No Travel Required

Not ApplicableNot Indicated

*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 CTA is an administrative support role for clinical trials. The role responsibilities include but not limited to the following activities:
Basically：
 Safety reports distribution and tracking.
 TMF support for country level document uploading to eTMF, assist with eTMF reconciliation, CDA collection, etc.
 Support HGRAC site filing documents collection and archiving.
 Coordinate with vendor for office supply purchasing, trial related documents printing and translation activity.
 Responsible for ABAC (Anti-Bribery and (Anti-)Corruption) check
 On site support for investigator meeting.
 Support CRM for tracker maintenance and run report from various systems and other activities based on CRM’s requirement.
 Contribute to CTA team knowledge by acting as mentor and/or sharing best practices, leading initiatives as required.
 Using IT technology to develop tool or work out solution to increase work efficiency and improve work accuracy will be preferred.
For the senior position:
 Take initiatives or POC and have leadership to support CTA managers or SMEs on process management or internal and external stakeholder management.

Current Contingent Workers apply

No Travel Required

Not ApplicableNot Indicated

Adaptability, Adaptability, Anti-Bribery and Corruption (ABC), Applied Engineering, Business Management, Clinical Information Systems, Clinical IT, Clinical Research, Clinical Research Ethics, Clinical Site Management, Clinical Site Monitoring, Clinical Study Management, Clinical Testing, Clinical Trial Compliance, Communication, Data Analysis, Drug Development Research, Good Clinical Data Management Practice (GCDMP), Interpersonal Relationships, Management Process, Mentorship, New Technology Integration, Organizational Management (OM), Peer Mentoring, Project Management {+ 5 more}

*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 Overview
  • Drive the early planning, development, and lifecycle management of new product portfolio to ensure commercial success in a competitive market from a value access perspective.

• Key responsibilities
  • Proactively monitor external environment, customers, and competitors to identify access opportunities for new product portfolio.
  • Analyze unmet needs and market access dynamics in new target therapeutic areas for pipeline products.
  • Identify value evidence needs and provide inputs to global R&D, value evidence generation, and access strategy planning from a China access perspective, and support global execution of relevant studies in China.
  • Timely provide input to cross-functional teams based on local access policies and dynamics.
  • Build long-term relationships with KOLs and industry associations in access.

• Qualifications
  • Master’s degree or higher in Pharmaceuticals, Life Sciences, Health Economics, and Pharmacy Administration, or related fields.
  • Experience: 8+ years in the pharmaceutical industry, deep knowledge of drug development processes, market access policies and HEOR. Experience in supporting new products is a plus.
  • Skills & Competencies: Strong analytical skills with Strategic thinking. Exceptional English and communication skills.

Current Contingent Workers apply

No Travel Required

Not ApplicableNot Indicated

*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

准入策略制定与执行

​安全运营策略

• 制定成熟产品的安全运营策略，包括院内保留列名及在院内管控期间推动解限，确保产品院内最大化患者可及性

​跨部门协作与项目管理

• 主导安全运营相关项目的全流程管理，包括设计，立项，落地及执行，确保关键KPI达成
• 协调内外部资源，推动安全运营策略一致性并落地整合实施

​内容设计与培训赋能

• 设计安全运营及EDL准入相关的核心材料，如政策解读工具包等，确保内容符合公司合规要求
• 组织内部培训与外部专家沟通会，提升团队对安全运营及准入政策的认知与执行能力

Current Contingent Workers apply

Not Applicable

*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

岗位职责：

• 执行公司年度招标策略方案，根据辖区各省情况，提出省级招标方案落地计划；
• 影响省级年度招标方案和目录，跟进年度招标关键节点，审核投标文件，参与现场（网上）开标，做好议价应对，推动所有产品的省级准入
• 配合公司准入产品策略：推动新产品、新剂型、新适应症的及时补标备案；
• 辖区各省的省级招标报价风险管理，省级招标风险预估及提出应对建议；
• 跨部门资源整合：GAMA（政务、KA、价格）/市场部/销售部等共同执行省份准入计划，共同搭建核心客户的市场活动平台；
• 整合外部资源：与商业公司、RDPAC等一起解决共性的招标问题
• 应对未来，提早准备，做好核心客户互动。加强省级招标重点客户拜访，包括省医保局，招采中心等；及时了解招标信息（招标政策方案等），省级招标相关政策沟通影响；搭建客户核心客户有效互动平台，加强省级招标相关客户有效互动

大客户管理经验，较强的客户沟通能力；

能力要求：

Current Contingent Workers apply

No Travel Required

Not ApplicableNot Indicated

*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

About the Role:

As a technical expert, this individual will utilize a variety of analytic software to integrate PK drug concentration-time measures, pharmacodynamic responses, and clinical safety and efficacy information for PK/PD and modeling and simulation (M&S) analyses. This individual will perform high-quality PMx analyses, including population PK modeling, PK-PD modeling, exposure-response analysis, and PBPK modeling to inform critical dose selection decisions in the early clinical development and support late development for regulatory filing.

Candidate Requirements:

• Ph.D. in pharmacometrics, pharmaceutical sciences, or related discipline with 2-4 (Manager) or 5+ (Sr. Manager) years of post-doctoral experience in a similar role in pharmaceutical drug development or academia.
• Expertise in pharmacometrics (like model-based meta-analysis, dose-response and exposure-response analyses, disease modelling, machine learning methods) with ability to understand how model-informed drug discovery can support regulatory decisions
• Deep knowledge of drug development, pharmacokinetics and pharmacology and basic science skills required
• Team spirit, bright, persistent, organized, and flexible.
• Fluent in both English and Chinese (oral and written).
• Proficiency in at least two of the following languages: NONMEM, R, Matlab/ SimBiology

Preferred Requirements:

• industry experience in drug development is preferred

Current Contingent Workers apply

No Travel Required

Not ApplicableNot Indicated

Adaptability, Adaptability, Biopharmaceuticals, Clinical Development, Clinical Research, Clinical Testing, Clinical Trial Development, Clinical Trials Monitoring, Clinical Trials Operations, Data Analysis, Dedication to Patient Care, Drug Development, Drug Discovery Process, Ethical Standards, Good Clinical Practice (GCP), ICH GCP Guidelines, Leadership Mentoring, Machine Learning Algorithms, Management Process, Medicinal Chemistry, Pharmaceutical Development, Pharmaceutical Research, Pharmaceutical Sciences, Pharmacodynamics, Pharmacokinetics {+ 5 more}

*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.