Associate Director, Study Patient Operations

1 miesiąc temu


Warsaw, Polska AstraZeneca Pełny etat

Location: Warsaw, Poland or Barcelona, Spain

Competitive Salary and Benefits

Make a more meaningful impact to patients’ lives around the globe

AstraZeneca’s R&D Data Office is an industry-leading enabler of data and AI strategy. The Data Office provides data services, technology, and data products, supported by data and AI policy and governance, to unlock the value of data that drive innovative science.
The Data Office’s Data Products and Platforms Team are responsible for the end-to-end hosting, processing and management of study and patient data, including clinical, imaging and omics data and associated study information, to enable cross R&D use; they will make data “FAIR” (Findable, Accessible, Interoperable and Reusable) and ensure the data is managed appropriately.


You will be responsible for managing the data, with both curation and operational aspect of data for the Data Office Products and Platform teams. 


Within the team you will work autonomously, supervising the work of others where needed, to ensure that the right study patient content is available to downstream users and is appropriately and compliantly managed. Your responsibilities include responding to and performing requests for study patient data services, including data operations such as data ingestion, curation, information completeness and reporting upon study and patient data assets. As a part of this execution, you will have oversight of automated flows into systems and catalogues, plus manual data stewardship and data management tasks.


You will take a strong customer oriented approach and achieve outcomes for requesters contributing to development of structured measures of operational activity (, operational metrics on data utilisation) and then use the information to actively contribute to the continuous improvement of study patient data services. When changes to processes are commissioned, you will ensure that these are appropriately documented, versioned and applied. Throughout these processes, you will make sure that operations align with associated data policies and standards, to help manage data risks, , data privacy risk. You are likely to have a background in pharma and being familiar with the set up, conduct and data managment of a clinical study.

Education, Qualifications, and Experience and skills:

Essential:

A university degree in a Computer Science, Data Management or other relevant subject area (Pharma, R&D, Finance, HR etc) and cross trained or equivalent number of years of experience  Hands-on experience from Agile development, preferably in a business context. Relevant degree in Information/Data Science, Computer Science, Informatics, IT, or other related discipline. Business Acumen (pharma and the life sciences): Understanding of the business domain (clinical studies and products) and industry trends, enabling effective decision-making and alignment of analytics initiatives with business goals. Demonstrable experience in a clinical data managment, data analyst or business analysis role aligned to data and information management with practical examples of performing data analysis, data management or data processing according to gathered requirements Business process mapping expertise: using as-is and to-be process mapping and ability to author requirements or other structured technical documents including supporting others in requirements analysis and data management activities Excellent communication skills and ability to build strong relationships Experience of running project in a GxP regulated environment Problem-solving: Ability to identify and resolve complex analytical and technical challenges, ensuring the accuracy and reliability of analytics solutions. Travel – willingness and ability to travel domestically & internationally.

Desirable:

Post-graduate degree in IT, Data Management Experience of achieving tangible and acknowledged value in a similar position and scale of challenge and opportunity.  Knowledge of Drug Discovery and Development practice in BioPharma Strong Change Management track record. Experience project manager with a great understanding of the project phase and the connection between classic project management and Agile ways of working Professional qualification in a specific subject area including Data Management or IT business analysis

Date Posted

21-maj-2024

Closing Date

14-cze-2024

  • Warsaw, Polska 9605 GSK Services Sp z o.o. Pełny etat

    We are building a Global Clinical Delivery Team within our hub based in Poland and looking for Associate Director Study Delivery Management who will lead a group of Study Delivery Specialists (SDSs) and Study Managers (SMs), who will perform tasks and activities in support of studies being delivered on time, at budget and within ICH-GCP quality framework....

  • Global Study Manager

    1 miesiąc temu


    Warsaw, Polska AstraZeneca Pełny etat

    Global Study Manager is a member of extended global study team supporting delivery of clinical studies within Global Medicines Development (GMD) to time, cost and quality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study archiving. The GSM works...

  • Global Study Manager

    4 tygodni temu


    Warsaw, Polska AstraZeneca Pełny etat

    Global Study Manager is a member of extended global study team supporting delivery of clinical studies within Global Medicines Development (GMD) to time, cost and quality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study archiving. The GSM works...


  • Warsaw, Polska AstraZeneca Pełny etat

    Locations: Barcelona, Spain (on-site) Warsaw, Poland (on-site) Mississauga, Canada (on-site) The Global Study Director (GSD) is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the operational planning and delivery of high priority and complex clinical studies or multiple...


  • Warsaw, Polska IQVIA Pełny etat

    IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle. The Patient Centered Solutions (PCS) team leads the industry in generating data to ensure that the patient voice is incorporated into the development and commercialization of medication and other drug/non-drug...


  • Warsaw, Polska AstraZeneca Pełny etat

    The Global Study Associate Director (GSAD) is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the delivery of clinical studies. The GSAD is responsible for leading a cross-functional study team and for providing the team with direction and guidance to enable successful study delivery....


  • Warsaw, Polska AstraZeneca Pełny etat

    The Global Study Associate Director (GSAD) is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the delivery of clinical studies. The GSAD is responsible for leading a cross-functional study team and for providing the team with direction and guidance to enable successful study delivery....

  • Global Study Manager

    1 miesiąc temu


    Warsaw, Polska AstraZeneca Pełny etat

    Global Study Manager is a member of extended global study team supporting delivery of clinical studies within Global Medicines Development (GMD) to time, cost and quality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study archiving. The GSM works...

  • Global Study Manager

    4 tygodni temu


    Warsaw, Polska AstraZeneca Pełny etat

    Global Study Manager is a member of extended global study team supporting delivery of clinical studies within Global Medicines Development (GMD) to time, cost and quality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study archiving. The GSM works...


  • Warsaw, Polska 1925 GlaxoSmithKline LLC Pełny etat

    Pharmacovigilance Scientists - Associate Director/ Director/ Senior Director Positions in GSK Safety Evaluation and Risk Management (SERM) - Specialty Safety Business. Exciting opportunities to make a significant impact on patients’ lives Provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK...


  • Warsaw, Polska 1925 GlaxoSmithKline LLC Pełny etat

    Pharmacovigilance Scientists - Associate Director/ Director/ Senior Director Positions in GSK Safety Evaluation and Risk Management (SERM) - Specialty Safety Business. Exciting opportunities to make a significant impact on patients’ lives Provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK...


  • Warsaw, Polska IQVIA Pełny etat

    Job Overview The medical department consists of a Chief Medical Officer, Medical Directors, medical writers, and safety associates. The Medical Director provides medical and scientific support to clinical research programs, study teams and investigators. The Medical Director also provides review, advice, and leadership for potentially or awarded clinical...


  • Warsaw, Polska AstraZeneca Pełny etat

    Associate Director, Statistical Programming, Late Stage Respiratory & Immunology Location : Warsaw (PL) Salary: Competitive, with excellent benefits. Hybrid model of work : 3 days in office, 2 days remote per week Reporting to: Director, Statistical Programming (Late Stage Respiratory & Immunology) Would you like to lead a Programming team,...


  • Warsaw, Polska AstraZeneca Pełny etat

    Associate Director, Statistical Programming, Late Stage Respiratory & Immunology Location : Warsaw (PL) Salary: Competitive, with excellent benefits. Hybrid model of work : 3 days in office, 2 days remote per week Reporting to: Director, Statistical Programming (Late Stage Respiratory & Immunology) Would you like to lead a Programming team,...


  • Warsaw, Polska 1925 GlaxoSmithKline LLC Pełny etat

    We’re excited to be moving to our vibrant new home on New Oxford Street in central London from the end of June 2024. At GSK HQ, we’re building an energising space where we can connect, collaborate and get ahead of disease together. Designed especially for us, it’ll be one of the healthiest workplaces in the world, with best-in-class tech and bright,...


  • Warsaw, Polska Precision Medicine Group Pełny etat

    Precision for Medicine is seeking an experienced Clinical Data Associate/Senior Clinical Data Associate to provide comprehensive data management support throughout all phases of the clinical trial data management process. Under direct supervision, you will ensure adherence to Standard Operating Procedures (SOPs), regulatory guidelines, and study-specific...


  • Warsaw, Polska IQVIA Pełny etat

    The Associate Director: Attack Surface Reduction role presents a dynamic opportunity to ensure the secure operation of the IQVIA global information technology (IT) infrastructure and processes through developing and implementing new cybersecurity safeguards, amending and improving existing safeguards, as well as contributing to implementation of necessary...

  • Wicedyrektor szkoły

    19 godzin temu


    Warsaw, Polska NOVA STUDY sp. z o.o. Pełny etat

    Wicedyrektor szkoły Miejsce pracy: Warszawa Twój zakres obowiązków Planning and ensuring the implementation of the Polish program at NS Preparation of the year plan, study schedule Selection, management and development of teachers of the Polish program. Maintaining school documentation Participation in events for teachers, self-development and...


  • Warsaw, Polska AstraZeneca Pełny etat

    Statistical Programming Associate Director, Late Stage Respiratory & Immunology Location : Warsaw (PL) Salary: Competitive, with excellent benefits. Hybrid model of work : 3 days in office, 2 days remote per week Reporting to: Director, Statistical Programming (Late Stage Respiratory & Immunology) Would you like to lead clinical studies,...


  • Warsaw, Polska AstraZeneca Pełny etat

    Statistical Programming Associate Director, Late Stage Respiratory & Immunology Location : Warsaw (PL) Salary: Competitive, with excellent benefits. Hybrid model of work : 3 days in office, 2 days remote per week Reporting to: Director, Statistical Programming (Late Stage Respiratory & Immunology) Would you like to lead clinical studies,...