Aktualne oferty pracy związane z Clinical Research Coordinator - Warszawa, Mazovia - ICON
-
Clinical Research Coordinator
3 tygodni temu
Warszawa, Mazovia, Polska PharmiWeb: Global Life Science Jobs Pełny etatAre you looking to drive groundbreaking medical research and make a real impact? Join our client as a Clinical Research Coordinator and lead the way in advancing clinical researchHobson Prior is seeking a Clinical Research Coordinator for a part-time freelance role in Warsaw. This position requires someone with experience in coordinating clinical studies at...
-
Clinical Research Coordinator
3 tygodni temu
Warszawa, Mazovia, Polska Hobson Prior International Ltd Pełny etatAre you looking to drive groundbreaking medical research and make a real impact? Join our client as a Clinical Research Coordinator and lead the way in advancing clinical researchHobson Prior is seeking a Clinical Research Coordinator for a part-time freelance role in Warsaw. This position requires someone with experience in coordinating clinical studies at...
-
Clinical Research Coordinator Role
5 dni temu
Warszawa, Mazovia, Polska beBee Careers Pełny etatAre you looking to drive groundbreaking medical research and make a real impact?This part-time freelance Clinical Research Coordinator role in Warsaw requires someone with experience in coordinating clinical studies at research sites.The successful candidate will be responsible for managing clinical trials, handling data entry, and resolving data-related...
-
Clinical Research Coordinator
7 dni temu
Warszawa, Mazovia, Polska beBee Careers Pełny etatJob Title: Clinical Research CoordinatorThe Clinical Research Coordinator works with various teams to provide administrative support for clinical trial activities through all phases of the lifecycle. They ensure timely completion, quality, and customer satisfaction.Key Responsibilities:Site Activation: Coordinate the preparation of Investigator Sites by...
-
Clinical Research Coordinator
1 tydzień temu
Warszawa, Mazovia, Polska beBee Careers Pełny etatJob DescriptionWe are seeking an experienced Clinical Research Coordinator to join our team. As a key member of our team, you will be responsible for providing administrative and coordinating support for site activation activities and other site level deliverables through all phases of the clinical trial lifecycle.About the PositionIn this role, you will...
-
The Role of a Clinical Research Coordinator
3 tygodni temu
Warszawa, Mazovia, Polska ICON Pełny etatThe Role of a Clinical Research CoordinatorClinical research plays a crucial role in advancing medical knowledge and improving patient care. At the heart of every successful clinical research study is a Clinical Research Coordinator (CRC). As a CRC, you serve as the linchpin between researchers, study participants, and regulatory bodies.In this comprehensive...
-
Clinical Research Coordinator II Lead
1 tydzień temu
Warszawa, Mazovia, Polska beBee Careers Pełny etatJob Overview">We are seeking a highly skilled Clinical Research Coordinator II Lead to join our team. In this role, you will oversee the development and maintenance of clinical study tools and templates, including the Clinical Monitoring Plan.">You will also coordinate initial and ongoing training to the study team regarding protocol specificities, Case...
-
Clinical Research Associate
6 dni temu
Warszawa, Mazovia, Polska beBee Careers Pełny etatAbout the RoleWe are seeking a highly organized and detail-oriented Clinical Research Coordinator to support Investigator Site staff in conducting clinical research studies according to project-specific requirements and regulatory guidelines.The successful candidate will serve as the primary point of contact for Investigator Site Staff and Sponsor...
-
Senior Clinical Research Coordinator
6 dni temu
Warszawa, Mazovia, Polska beBee Careers Pełny etatAs a Senior Clinical Research Coordinator, you will play a key role in planning, executing, managing and monitoring clinical research projects. You will be responsible for adapting existing templates and processes to meet the needs of regional, single modality or therapeutic area projects.Key ResponsibilitiesProject PlanningDevelop and implement project...
-
Advanced Clinical Trials Coordinator Role
6 dni temu
Warszawa, Mazovia, Polska beBee Careers Pełny etatJob OverviewWe are seeking a part-time freelance Clinical Research Coordinator for a role in Poland.This position requires experience in coordinating clinical studies at research sites and ensuring smooth operations and data management within clinical trials.Key Responsibilities:Manage clinical trials at the research site to ensure successful...
Clinical Research Coordinator
1 miesiąc temu
Clinical Research Coordinator - Bielsko-Biala/Ustron, Poland - office-based
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Clinical Research Coordinator is responsible for supporting Investigator Site staff in conducting clinical research studies according to project-specific requirements and regulatory guidelines.
The role involves assisting in study-related activities at the site level, ensuring compliance with protocols, Standard Operational Procedures (SOPs), and international and local clinical trial regulations (ICH GCP Guidelines, CFR, GDPR, HIPAA, etc.).
Location: Bielsko-Biala/Ustron, Poland
Part-time contract
What You Will Be Doing:
- Serve as a primary point of contact for Investigator Site Staff and Sponsor representatives.
- Support organization and execution of monitoring visits and audits at the Investigator Site, including arranging visits, preparing documentation, and coordinating with relevant site personnel.
- Enter patient-specific data into applicable clinical systems (eCRF, ASM, etc.) and assist in resolving data queries.
- Arrange and coordinate patient visits and communication.
- Collaborate with external service providers, such as central laboratories and couriers.
- Maintain assigned sections of the Investigator Site File and patient documentation.
- Participate in internal meetings and teleconferences.
- Assist with additional study-related tasks as per the Investigator's requirements.
- Report any issues encountered during site operations to the Line Manager.
- Prepare reports on completed activities as per established timelines.
- Perform a wide range of administrative tasks connected to the assigned studies, mainly working with eCRF (data entry, query resolution), ISF maintenance, being the first point of contact for the CRA, monitoring visit support, etc.
- Perform other duties as assigned by the direct Line Manager.
Your Profile:
- Bachelor's degree in a relevant field such as business administration, project management, or a related discipline.
- Experience in a similar role or environment, with a focus on oncology project support.
- Strong analytical skills and attention to detail, with the ability to work effectively in a team.
- Excellent communication and interpersonal skills, with a collaborative approach to problem-solving.
- Proficiency in relevant software applications and tools to support project execution.
What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work-life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family's needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we've done to become a more inclusive organisation. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply.
#J-18808-Ljbffr