Clinical Systems Specialist-POLAND
2 tygodni temu
The Clinical Systems Specialist is responsible for providing support to internal end users for the Clinical Systems including training, troubleshooting, reporting, and managing user access.
More specifically, the Clinical Systems Specialist:
- Manage and support the Clinical Systems, including system implementation, set-up, maintenance, support, training, testing, and documentation;
- Manage user access to the system;
- Program reports and dashboards;
- Assess the training needs of end users and design effective training materials and techniques for individuals with different levels of computer literacy;
- Conduct software application trainings to end users;
- Research, interpret, explain and apply information from computer software technical manuals and guides, videos and online materials;
- Develop an in-depth understanding of operational workflows in order to develop and implement system processes;
- Support end users by providing technical support, troubleshooting and identifying opportunities for system improvements;
- Communicate with vendor for system support, development, improvement, and maintenance;
- Respond to client audits and questions;
- Prepare, execute, and document all aspects of Validation Testing for the system;
- Provide routine or ad-hoc reports to executives;
- Collaborate with other Department/Teams to integrate processes/systems;
- Review billing requests from Vendors.
Employee may be assigned to other responsibilities that do not pertain to their former description, if they have the required experience, are qualified and/or have received adequate training.
Requirements:
- Post-secondary education;
- 3-5 years of relevant experience;
- Previous experience working in a CRO, pharmaceutical or biotechnology industry, an asset;
- Proven expertise working with Sharepoint (support, configuration, and programming);
- Excellent knowledge of the Microsoft Office Suite;
- Good knowledge of MS Reporting Services;
- Good understanding of working in a controlled and validated environment;
- Ability to develop training material and conduct training sessions for end users;
- English- excellent oral and written skills;
- Good organizational and prioritization skills;
- Ability to work in a fast-paced environment;
- Meticulous attention to detail and accuracy;
- Ability to troubleshoot and resolve issues effectively;
- Ability to work in a team environment and establish good relationships with colleagues.
- Good knowledge of good clinical practices, GxP and applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines.
Our company:
The work environment
At Indero, you will work with brilliant and driven professionals. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.
As a Clinical Systems Specialist you will be eligible for the following perks:
- Permanent full-time position
- Flexible schedule
- Vacation
- Home-based position
- Ongoing learning and development
About Indero
Indero is a contract research organization (CRO) specialized in dermatology and Rheumatology. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Indero continues to grow and expand in North America and Europe.
Indero is committed to providing equitable treatment and equal opportunity to all individuals. As such, Indero will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.
Indero only accepts applicants who can legally work in Poland.
Brand name:
Indero
-
eCOA & RTSM Application Specialist (Poland)
1 dzień temu
zdalnie, Polska Indero Pełny etatThe eCOA and RTSM Application Specialist is responsible for supporting the design, deployment, configuration, and oversight of electronic Clinical Outcome Assessment (eCOA) solutions—including ePRO, eConsent, and other patient-centric electronic data capture tools— and of Randomization and Trial Supply Management (RTSM) across global clinical...
-
Senior Clinical Data Manager
1 tydzień temu
zdalnie, Polska Indero Pełny etat 60 000 zł - 120 000 zł rocznieAs a Senior Clinical Data Manager, you will ensure that data captured in multiple clinical trials undertaken or managed by Indero is collected, managed, and reported clearly, accurately and securely.This role will be perfect for you if:You want to work on studies end-to-end (involved from protocol review to database lock)You have the experience and...
-
Regulatory Affairs Specialist-POLAND
1 tydzień temu
zdalnie, Polska Indero Pełny etat 40 000 zł - 80 000 zł rocznieDue to ongoing global expansion, Indero is looking to hire a Regulatory Affairs Specialist. In this position, you will be responsible for preparation and submission of part I and/or part II following EU CTR and other applications created within or outside of the company to ensure documentation comply with applicable regulations and guidelines and contractual...
-
Senior Clinical Data Coordinator
1 tydzień temu
zdalnie, Polska Indero Pełny etat 40 000 zł - 80 000 zł rocznieThe Senior Clinical Data Coordinator will participate in various clinical data management activities required to ensure that data captured in clinical trials undertaken, or managed by Indero, are collected, managed, and reported clearly, accurately and securely. In addition, this position is required to conduct all these activities in conformance with...
-
Freelance Regional Clinical Trial Coordinator
1 tydzień temu
zdalnie, Polska RHO Inc Pełny etat 40 000 zł - 60 000 zł rocznieWe are seeking a detail-oriented and collaborative Regional Clinical Trial Coordinator (RCTC) to support the execution of clinical trials at the site level. This role ensures operational excellence through administrative coordination, documentation oversight, and system management in compliance with ICH-GCP and local regulations.Key...
-
Senior Regulatory Affairs Specialist
7 dni temu
zdalnie, Polska Indero Pełny etat 100 000 zł - 150 000 zł rocznieThe Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions.This role will be responsible for sponsor-facing regulatory leadership and management of regulatory deliverables...
-
External Sales Representative Poland
2 tygodni temu
zdalnie, Polska Electrical Safety & Instrumentation Specialists Ldt (ESIS) Pełny etat 160 000 zł - 190 000 zł rocznieAbout ESIS Ltd.ESIS Ltd. (Electrical Safety & Instrumentation Specialist Ltd.) is a leading technical solutions provider serving the electrical, industrial, OEM, and distribution sectors across Europe. We represent high-quality manufacturers and deliver specialist products, technical support, and customer-focused service.We are a growing and dynamic team...
-
CRM Systems
2 tygodni temu
zdalnie, Polska WestLink Pełny etat 40 000 zł - 60 000 zł rocznieAbout the RoleWe're looking for a CRM Systems & Automation Specialist to lead the full audit, cleanup, and optimization of our CRM environment.The ideal candidate will ensure our CRM operates as a clean, integrated, and reliable system that supports seamless workflows between Omniview, QuickBooks, and Outlook.You'll be responsible for establishing data...
-
Risk Manager
3 dni temu
zdalnie, Polska Indero Pełny etatThe Risk Manager plays a pivotal role in developing and executing risk-based monitoring strategies, ensuring data quality and integrity in clinical research projects. This position involves cross-functional collaboration to identify, assess, and mitigate risks throughout the clinical trial lifecycle, supporting the seamless implementation of Risk-Based Study...
-
Freelance Data Analyst, Poland
5 dni temu
zdalnie, Polska bb-8765-43b4-9ac1-7ab205575f0a Pełny etatJoin us in redefining what it means to work for a CRO.When you work at Rho, it's more than just a job—you become part of the Rho Factor. We're a proud bunch of science nerds who love tackling big challenges together. We're not your typical CRO, and we're not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at...