Clinical Research Coordinator - Bydgoszcz

IQVIA Inc; Bydgoszcz; Ibrido; PLN 83.000 - 154.000; Part-time

Descrizione del lavoro

IQVIA Inc. is seeking a Clinical Research Coordinator in Bydgoszcz, Poland. This 24-hour per week role supports a clinical site for an initial ~6-month period, with immediate start.

You will prescreen participants, maintain study docs, support patient screening and enrollment, manage IP and inventory, and coordinate lab shipments and EMR certification. Ideal candidates hold a life sciences degree and have at least 2 years of clinical research assistant/coordinator experience, strong English, and

Competenze

• Bachelor’s degree in life sciences or equivalent.
• Experience in clinical research coordination or related role.
• Familiarity with study protocols, consent forms, and schedules.
• Experience with lab samples processing and IRT/IWRS systems.
• Excellent communication and organizational skills; fluent in English.

Mansioni

• Assist in prescreening and screening tasks and patient enrollment.
• Maintain study documents, CRFs, EDC, and eTMFs.
• Coordinate study procedures and communications with monitors.
• Manage IP accountability, inventory, and lab shipments.
• Provide administrative and patient scheduling support.

Conoscenze

Clinical research experience

English fluency

Communication skills

Organizational skills

Attention to detail

Formazione

Bachelor’s degree in life sciences

Strumenti

IRT/IWRS systems

MS Office

EMR systems

Descrizione del lavoro

Clinical Research Coordinator - Bydgoszcz### Clinical Research Coordinator - BydgoszczApply: Bydgoszcz, Poland: Part time: Posted Today: R1577170**Clinical Research Coordinator in Bydgoszcz** **Working Hours:** 24 hours per week**Start Date**: Immediately **Duration**: Approximately 6 months IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Bydgoszcz .This **24h hour per week** role offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment. **Key Responsibilities**As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including: * Prescreening and Screening tasks* Review charts from the site data base* Maintaining and updating study documentation, including protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems and eTMFs* Supporting patient screening and enrollment, including handling informed consent and privacy documentation* IP - site accountability including IP - patient compliance* Use of IRT/IWRS systems for subject randomization, investigational product assignment, inventory management, and site-level clinical trial operations* Processing and shipment of lab samples process* Patient scheduling support* Printing and certifying EMR* Coordinating logistical activities for study procedures in line with the study protocol* Communicating with study monitors and responding to study-related inquiries* Carrying out general administrative tasks related to the study **Your Profile** We are looking for candidates who bring a combination of education, experience, and skills:* Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)* Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules* Experience with lap samples and IRT/IWRS systems* Good knowledge of medical terminology* Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)* **Must have at least 2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site*** Excellent interpersonal and communication skills* Strong organizational skills and attention to detail* Fluency in English **Why Join IQVIA?** At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference. **Interested?** If this sounds like the right opportunity for you, we encourage you to apply today. #LI-HCPN#LI-CES#LI-DNP#LI-NS#LI-OnsiteIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.The potential base pay range for this role, when annualized, is zł83,000.00 - zł154,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.