Clinical Supply Specialist

hace 2 semanas

Desde casa, México Parexel A tiempo completo

**Primary Location**: Mexico, Remote**Additional Locations**: Argentina, Remote; Brazil, Remote**Job ID** R **Category** Clinical Logistics**ABOUT THIS ROLE**:The CSS/Senior CSS has responsibility for the execution of the clinical trial supply logistics strategy on the project.**Key Accountabilities**:**Project Management**- Engaging with Clinical Supply Leader to develop logistics concepts and solutions in order to meet the client’s satisfaction and meeting the- profitability of the projects- Keeping up to date with study scope and progress to ensure that study/project timelines and budgets are met in accordance to the contractual agreement including proactive management and communication of any changes and/or risks.- Ensure that study specific management tools and documents are in place- Management of own resources assigned to the project to ensure the CTSL FTE assigned is appropriate and meeting the study’s requirement**Financial Management**- Pass Thru Cost (PTC) management with controls and reporting of costs for internal service fees and external providers.**Operational Strategy and Management**- Collaborate with team to develop a clinical supply, sourcing and distribution strategy with relevant stakeholder and make sure that required documentation is in place- Communicate with 3rd party providers and negotiate scope of work in conjunction with procurement.- Develop and plan inventory according to strategy, quantities and forecast- Develop supply schedule, seek feedback from Clinical team on study progress and adjust accordingly and provide feedback to depots**(Senior) Ensure Quality and Process Improvement**- Identify and initiate process improvements- Mentoring of Clinical Supply Specialists and Clinical Supply Assistants**Skills**:- Client focused approach to work- Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail- Proven consultative selling and negotiation, communication and customer management skills.- Ability to support team members.- Ability to develop creative solutions.- Sound/Excellent operational understanding.- Self- Motivated with a professional attitude.- Capacity to work effectively in a matrix environment and value the importance of teamwork.- Basic Project management skills- Proficient use of MS office suite- Excellent interpersonal, verbal and written communication skills- Good/Very good understanding of the GxP regulatory framework**Knowledge and Experience**:- Extensive experience of pharmaceutical/Clinical research/consulting industry.- Profound/Superior experience in clinical logistics or related field within the biopharmaceutical industry.- Project management experience- Individuals should have a strong understanding of cross functional activities- Profound multinational work experience.- Fluent in English**Education**:- Educated to B.A/ B.S. or Master degree, or equivalent (e.g. Pharm. D.), in biology, pharmacy, or other health -related discipline, international trade, business administration or logistics or relevant work experienceLI-REMOTE

  • Manager of Clinical Supplies

    hace 5 días

    Desde casa, México ICON A tiempo completo

    As a Manager of Clinical Supplies you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: - Represent Clinical Supply Chain on Clinical Study Teams and provide a high service level to internal stakeholders. - Works with Clinical Operations to understand...

  • Senior Clinical Specialist

    hace 3 semanas

    Desde casa, México Signant Health A tiempo completo

    (This is a remote role located in Mexico)*****Want to do the Best Work of Your Life?**Working at Signant Health puts you at the very heart of the world’s most exciting sector - a high-growth, dynamic company in an extraordinary industry. We’re radically changing the clinical trial landscape, driving change through the technology and innovations we create...

  • Clinical Quality Compliance Specialist

    hace 2 semanas

    Desde casa, México ICON A tiempo completo

    As a Clincial Quality Compliance Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: - Under the leadership of the Operations Quality Lead, develop, contribute, and support facilitation, presentation, and communication of GCP Lessons Learned, GCP...

  • Senio Clinical Data Specialist, Latam

    hace 3 semanas

    Desde casa, México IQVIA A tiempo completo

    **POSITION TITLE**: Senior Clinical Data Specialist**REPORTS TO**: Associate Manager/Manager, Data Management or Designee**BASIC FUNCTIONS**:**ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES**:- Clinical Data and Query Review:- Create listings using ad hoc query tools- Issue queries and review query responses with the highest level of quality based upon...

  • Clinical Data Specialist

    hace 2 semanas

    Desde casa, México IQVIA A tiempo completo

    **Job Overview** Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager....

  • Clinical Supplies Project Manager

    hace 5 días

    Desde casa, México ICON A tiempo completo

    **Clinical Supplies Project Manager** ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we...

  • Clinical Research Associate

    hace 2 semanas

    Desde casa, México Parexel A tiempo completo

    Parexel is looking for multiple **CRAs** with 1+ year of experience in Mexico!The **Clinical Research Associate**will be responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted in line with the Study Monitoring Plan and will be performed virtually for the...

  • Regulatory Affairs Specialist

    hace 2 semanas

    Desde casa, México ICON A tiempo completo

    As a Regulatory Affairs Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: - Regulatory advice to drug development is key to ensuring our clients pursue first time right strategies to overall product development and to clinical programme...

  • Systems Validation Specialist Ii

    hace 2 semanas

    Desde casa, México Parexel A tiempo completo

    Mexico, Remote**Job ID** R **Category** Quality Management**ABOUT THIS ROLE**:We are seeking a System Validation Specialist to join our SVS team. This role will support and improve the compliance of our technology solutions by implementing standardized, harmonized, and streamlined validation/qualification activities based on current GxP requirements and risk...

  • Regulatory Affairs Specialist

    hace 2 semanas

    Desde casa, México ICON A tiempo completo

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...