Clinical Research Site Specialist

ICON Clinical Research Clinical Research Coordinator (Przemysl, Poland) in Warsaw, PolandClinical Research Coordinator - Przemysl, Poland - FTICON 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...

Job SummaryCare Access Research is seeking a highly skilled and experienced Clinical Research Site Manager to oversee the day-to-day activities at our research site in Warsaw, Poland. As a key member of our team, you will be responsible for ensuring the successful execution of clinical trials, maintaining adherence to local regulations and Care Access SOPs,...

Experienced Clinical Research Associate (CRA)August Research, an Everest Clinical Research company, is looking for an experienced Clinical Research Associate (CRA) to join our team in Warsaw, Poland.This is a full-time CRA position for a candidate with at least one year of monitoring experience. Job responsibilities will include site identification and site...

Clinical Research Coordinator is a critical member of the investigative site team, responsible for ensuring the successful conduct of clinical research studies according to project-specific requirements and regulatory guidelines.This role involves assisting in study-related activities at the site level, ensuring compliance with protocols, Standard...

Career OverviewAugust Research, an esteemed clinical research company, seeks a highly experienced Clinical Research Associate (CRA) to join its team in Warsaw, Poland.

Clinical Research Coordinators play a vital role in supporting Investigator Site staff in conducting clinical research studies according to project-specific requirements and regulatory guidelines.The Clinical Research Coordinator is responsible for assisting in study-related activities at the site level, ensuring compliance with protocols, Standard...

Clinical research is a vital component of the healthcare industry, and professionals who excel in this field are in high demand. At ICON plc, we're proud to offer exciting opportunities for individuals to join our team as Clinical Research Coordinators.We're looking for talented and motivated individuals to support Investigator Site staff in conducting...

Clinical Research Associate (en)ICON plc is a leading healthcare intelligence and clinical research organization that fosters an inclusive environment driving innovation and excellence.The Clinical Research Associate role involves supporting Investigator Site staff in conducting clinical research studies according to project-specific requirements and...

As a Clinical Research Coordinator at ICON plc, you will play a critical role in supporting Investigator Site staff in conducting clinical research studies. This involves assisting in study-related activities at the site level, ensuring compliance with protocols, Standard Operational Procedures (SOPs), and international and local clinical trial...

Clinical Research Coordinator is a key role in supporting Investigator Site staff in conducting clinical research studies according to project-specific requirements and regulatory guidelines.The successful candidate will be responsible for assisting in study-related activities at the site level, ensuring compliance with protocols, Standard Operational...

About UsAt Thermo Fisher Scientific, we're dedicated to enabling our customers to make the world a healthier, cleaner, and safer place. With a global presence and a team of over 100,000 colleagues, we share a common set of values - Integrity, Intensity, Innovation, and Involvement. Our mission is to accelerate research, solve complex scientific challenges,...

Job Description:Indero, a renowned CRO in dermatology and rheumatology, seeks a skilled Project Coordinator to support site activation activities and other deliverables through the clinical trial lifecycle. This role is ideal for individuals with experience in project administration and clinical research.About the Role:We are looking for an organized and...

Clinical Research Associate Role DescriptionThe Clinical Research Associate will be responsible for performing monitoring and site management work to ensure the successful conduct of clinical trials. This includes:Conducting site initiation, monitoring, and close-out visitsMaintaining accurate and complete records of site activitiesDeveloping and...

Job OverviewAt Comac Medical, we are seeking a skilled Clinical Research Associate to play a key role in the success of our clinical trials. As a Clinical Research Associate, you will be responsible for conducting feasibility studies and site qualification visits, developing strong relationships with investigators, and ensuring compliance with regulatory...

Job DescriptionThe ideal candidate will have a graduate or postgraduate degree in a relevant field, preferably biology, pharmacy, or chemistry. At least 3 years of experience as a clinical research associate or monitor is required.Key responsibilities include:Conducting feasibility studies and site qualification visitsDeveloping and maintaining strong site...

About the RoleWe are seeking an experienced Research Facility Manager to join our team in Warsaw, Poland. As a key member of our operations team, you will be responsible for overseeing the day-to-day activities at our research site and driving enrollment goals. You will work closely with our Country Manager to ensure the successful execution of clinical...

Job DescriptionWe are seeking a highly skilled Clinical Research Operations Specialist to join our team. The successful candidate will be responsible for providing operational and administrative support for study delivery activities.Key ResponsibilitiesManage study execution from start-up through close-out in accordance with study timelinesCoordinate study...

Clinical Research Coordinator is a key member of the investigative site team, responsible for supporting the conduct of clinical research studies according to project-specific requirements and regulatory guidelines.This role involves assisting in study-related activities at the site level, ensuring compliance with protocols, Standard Operational Procedures...

Requirements and QualificationsBachelor's degree in computer science, Statistics, Mathematics, Life Sciences or other relevant scientific fields.Minimum 5 years of experience in developing software in a clinical trial environment using SQL, including at least 3 years of clinical programming experience.Strong programming skills in a relational database...

Clinical Research Coordinators at ICON plc play a critical role in ensuring the smooth operation of clinical trials by supporting Investigator Site staff in conducting clinical research studies according to project-specific requirements and regulatory guidelines.We're looking for a highly skilled and motivated individual to join our team as a Clinical...