Aktualne oferty pracy związane z R/SQL Developer in Clinical Trials - Warszawa, Mazovia - PSI CRO AG

  • Clinical Programmer

    4 tygodni temu

    Warszawa, Mazovia, Polska Advanced Clinical Pełny etat

    Brief DescriptionThe Clinical Programmer will be responsible for the provision of data review and trial management deliverables across all compounds and trials for which these are required, and for all functional groups that require those deliverables.Essential Functions/ResponsibilitiesProgram simple to complex data review listings, exception reports,...

  • Technical Lead, Clinical Trials Business

    4 dni temu

    Warszawa, Mazovia, Polska IQVIA Argentina Pełny etat

    Job Title: Technical Lead, Clinical Trials BusinessAbout the JobWe are seeking a Technical Lead, Clinical Trials Business to lead the design and development of data science applications that support clinical trials business. The successful candidate will have a strong background in software development and data science, with a proven track record of success...

  • Clinical Trials Manager Assistant

    2 tygodni temu

    Warszawa, Mazovia, Polska Hobson Prior International Ltd Pełny etat

    Drive groundbreaking medical research forward as a Clinical Research Coordinator with Hobson Prior International Ltd.This part-time freelance role in Warsaw requires an experienced professional to coordinate clinical studies at research sites, ensuring smooth operations and data management within clinical trials.The successful candidate will have a strong...

  • Research Coordinator

    2 tygodni temu

    Warszawa, Mazovia, Polska TN Poland Pełny etat

    Research Coordinator - Clinical TrialsWe are seeking a highly skilled Research Coordinator - Clinical Trials to join our team at Thermo Fisher Scientific. In this role, you will be responsible for providing technical support to our clinical research team, ensuring the smooth execution of clinical trials.About the Position:This is a client-dedicated position,...

  • SAS Programmer in Clinical Trials

    4 tygodni temu

    Warszawa, Mazovia, Polska PSI CRO Pełny etat

    We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.Job...

  • Clinical Trials Support Professional

    2 tygodni temu

    Warszawa, Mazovia, Polska ICON plc Pełny etat

    Role SummaryThe Clinical Trials Support Professional role is responsible for supporting the collection, documentation, and reporting of safety data related to medications and clinical trials. This role requires strong organizational skills, attention to detail, and effective communication and collaboration skills.Key Responsibilities:Support the collection,...

  • Clinical Trials Management Specialist

    1 tydzień temu

    Warszawa, Mazovia, Polska Care Access Research Pełny etat

    About the RoleCare Access Research seeks a Clinical Trials Management Specialist to join our team. As a key member of our operations team, you will be responsible for overseeing the day-to-day activities at a clinical research site, ensuring delivery of enrollment goals while maintaining adherence to local regulations and SOPs.This is an exciting opportunity...

  • Project Manager in Clinical Trials

    9 godzin temu

    Warszawa, Mazovia, Polska beBee Careers Pełny etat

    Key ResponsibilitiesThe successful candidate will be responsible for monitoring study timelines, patient recruitment, and budget at the start-up phase. They will also participate in bid defense, client, investigator, and team meetings.This role requires strong leadership skills, with the ability to manage multiple projects simultaneously and prioritize tasks...

  • Clinical Trials Manager

    5 dni temu

    Warszawa, Mazovia, Polska TN Poland Pełny etat

    Job DetailsThe Clinical Trials Manager role involves managing the execution of assigned clinical studies from initiation through to closeout. As a Centralized Monitor, you will be responsible for reviewing and managing study-specific analytics based on applicable study-specific plans and contributing to developing new analytics proposals as per customer's...

  • Administrative Assistant Clinical Trials

    2 tygodni temu

    Warszawa, Mazovia, Polska Parexel International Pełny etat

    Administrative Assistant Clinical Trials Role SummaryWe are seeking an experienced Administrative Assistant to support our Clinical Trials team. The successful candidate will provide high-quality administrative support, maintaining the highest level of professionalism and discretion.ResponsibilitiesAdministrative Tasks: Providing administrative support to...

  • Clinical Trials Logistics Manager

    3 dni temu

    Warszawa, Mazovia, Polska TN Poland Pełny etat

    Clinical Supply Chain Manager Key ResponsibilitiesThe Clinical Supply Chain Manager is responsible for leading the clinical supply chain team and ensuring timely delivery of trial materials.This involves managing interactions with internal and external stakeholders, creating effective solutions, and ensuring compliance with all relevant regulations.Key...

  • Clinical Trials Specialist

    5 dni temu

    Warszawa, Mazovia, Polska PSI CRO Pełny etat

    Company OverviewPSI CRO is a leading Contract Research Organization with over two decades of experience in the industry, offering a unique blend of stability and innovation to both clients and employees.We focus on delivering high-quality services across various therapeutic areas.Job DescriptionAs a PSI CRO Medical Monitor, you will provide critical medical...

  • SAS Programmer in Clinical Trials and Beyond

    2 tygodni temu

    Warszawa, Mazovia, Polska PSI CRO Pełny etat

    About UsPSI CRO is a dynamic, global company that cares about its employees. We are seeking a highly skilled SAS Programmer in Clinical Trials and Beyond to join our team. In this role, you will work with clinical trials patient and operational data, developing new data solutions and setting up Risk-based Monitoring systems.You will participate in the...

  • Clinical Trials Coordinator

    3 dni temu

    Warszawa, Mazovia, Polska ICON plc Pełny etat

    About ICON plcWe're a world-leading healthcare intelligence and clinical research organization. Our mission is to shape the future of clinical development by fostering an inclusive environment that drives innovation and excellence.We're currently seeking a Logistics Coordinator I to join our diverse and dynamic team. As a Logistics Coordinator I at ICON, you...

  • Global Clinical Trials Coordinator

    6 dni temu

    Warszawa, Mazovia, Polska Merck Sharp & Dohme Corp. Pełny etat

    Work ExperienceWe are looking for candidates with:Min. 1 year of experience in clinical trials.Proven skills in site management, including management of site performance and patient recruitment.Good IT skills, ability to learn and operate new IT applications.Ability to understand and analyze data/metrics.RequirementsFluent in English (verbal and written) and...

  • Research Associate

    9 godzin temu

    Warszawa, Mazovia, Polska beBee Careers Pełny etat

    **About the Role:**This is an exciting opportunity to join our clinical trials team as a Site Management Specialist. As a key member of the team, you will be responsible for managing trial sites, ensuring compliance with regulatory requirements, and collaborating with internal stakeholders.You will work closely with the Local Trial Manager (LTM), Clinical...

  • Clinical Trials Manager Position

    1 tydzień temu

    Warszawa, Mazovia, Polska PSI CRO AG Pełny etat

    **About the Role**We are looking for a motivated Senior Clinical Trial Specialist to become a part of our international team at PSI CRO AG.The successful candidate will be responsible for providing feasibility services, contributing to the development of the company's business, and ensuring smooth and predictable conduct of newly awarded trials.Conduct...

  • Contract Specialist for Clinical Trials

    1 tydzień temu

    Warszawa, Mazovia, Polska BlueSnap, Inc Pełny etat

    About the RoleWe are seeking a highly skilled and experienced Contract Specialist for Clinical Trials to join our team. As a key member of the Site Selection and Contracting team, you will be responsible for preparing, negotiating, and executing contracts and budgets with investigator sites.This is an exciting opportunity for a motivated and organized...

  • Operational Excellence Associate for Clinical Trials

    2 tygodni temu

    Warszawa, Mazovia, Polska Pfizer, S.A. de C.V Pełny etat

    Operational Excellence Associate for Clinical TrialsWe're looking for an experienced Operational Excellence Associate to join our Clinical Trials team at Pfizer. In this role, you will be responsible for the operational execution and oversight of our Clinical Trial Data Sharing (CTDS) program.The Operational Excellence Associate will serve as a point of...

  • SAS Programming Expert

    2 tygodni temu

    Warszawa, Mazovia, Polska IQVIA Argentina Pełny etat

    This is an exciting opportunity to join IQVIA Argentina as a SAS Programming Expert - Clinical Trials, where you will play a key role in developing and implementing programming scripts for data retrieval, transformation, and representation.Job DescriptionIn this position, you will collaborate with interface departments such as Biostats and Data Management to...

R/SQL Developer in Clinical Trials

1 miesiąc temu

Warszawa, Mazovia, Polska PSI CRO AG Pełny etat

Company Description
We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description
Actual Position name: Clinical Data Scientist
Reporting to the Clinical Data Science Manager, the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data, develop new data solutions and set up Risk-based Monitoring systems in Process Improvement department.
Hybrid work in Sofia.

  • Participate in selection of the Risk-Based Monitoring (RBM) system and provide relevant training to the project team and/or Sponsor.
  • Set up and maintain RBM systems, collaborating with the Central Monitoring Manager.
  • Manage complex datasets from multiple sources, including data extraction, transformation, and loading into PSI data platform.
  • Program and produce data listings, tables, and figures for Clinical Data Reviewers and Central Monitoring Managers.
  • Calculate Key Risk Indicators and Quality Tolerance Limits, applying advanced analytical techniques to identify data trends for Centralized Monitoring.
  • Collaborate cross-functionally to identify study challenges and develop data solutions using advanced analytics.
  • Communicate data findings and solutions to stakeholders effectively.
  • Contribute to the development of databases, software products, processes, and Quality System Documents for Centralized Monitoring.

Qualifications
Must have:

  • Degree in Data Science, Mathematics, Statistics, Computer Science or equivalent; or relevant work experience and professional qualifications.
  • At least 5 years of experience in Data Management, Biostatistics, and Centralized Monitoring.
  • At least 4 years of experience in one or more of the following: R, R Shiny, SAS, SQL and associated packages and libraries.
  • At least 2 years of experience in data engineering area including one or more of the following: relationship databases, data warehousing, data schemas, data stores, data modeling, testing, validation and analysis.
  • Full professional proficiency in English and Polish.
  • Strong analytical and logical thinking.
  • Communication and collaboration skills.

Nice to have:

  • Experience with CluePoints RBM system.
  • Knowledge of statistical methods and techniques for analyzing data.
  • Experience using Machine Learning techniques and products testing and validation.

Additional Information
What we offer:

  • We value your time so the recruitment process is as quick as 3 meetings.
  • We'll prepare you to do your job at the highest quality level with our extensive onboarding and mentorship program.
  • You'll have excellent working conditions - spacious and modern office in a convenient location, and a friendly, supportive team who love to hang out together.
  • You'll have a permanent work agreement at a stable, privately owned company.
  • We care about our employees - aside from competitive salary, you'll have good work-life balance with flexible working hours and additional days off, life and medical insurance, sports card, lunch card.
  • We're constantly growing which means opportunities for personal and professional growth.

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

Seniority level

Associate

Employment type

Full-time

Job function

Analyst

Industries

Pharmaceutical Manufacturing

#J-18808-Ljbffr