Clinical Trial Coordinator

Job Description:We are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our Clinical Operations team in Poland, Estonia, Lithuania, or Latvia. The successful candidate will have experience in Clinical Trials and possess excellent organizational, communication, and teamwork skills.Key Responsibilities:Preparation of ISFs...

OverviewJoin us in redefining what it means to work for a CRO. Working at Rho, you'll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity's biggest challenges.At Rho, we're committed to you just as you're committed to us. You'll have the opportunity to...

TN Poland is seeking a detail-oriented and organized individual to fill the role of Associate Site Manager.Responsibilities:The Associate Site Manager will be responsible for ensuring site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases.This role also involves contributing to site...

We are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our Clinical Operations team in Poland, Estonia, Lithuania, or Latvia. The successful candidate will have experience in Clinical Trials and possess excellent organizational, communication, and teamwork skills.Key Responsibilities:Preparation of ISFs (Investigator Site...

Are you an expert in graphic design looking to apply your skills in a fast-paced environment? Do you have a passion for creating visually appealing documents?We're seeking a highly skilled Clinical Trial Document Specialist to join our team at PSI CRO. As a specialist, you'll be responsible for designing and developing clinical trial documents that meet...

OverviewRho is a global contract research organization (CRO) dedicated to healthcare and clinical research. We take a personalized approach to working with our clients, understanding their unique needs and challenges.We are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our team in Poland, Estonia, Lithuania, or Latvia. As a...

RequirementsEducation BSN/BS/MS or BA required.Minimum of 1 year experience in clinical environment as CTA.Excellent written and oral communication skills.Knowledge of Microsoft Office applications especially Excel.Ability to collaborate and build strong partnerships/relationships with all functions involved in the trial.Fluent English.Why ICON?Our success...

About the Role:The Global Study Manager will be responsible for managing clinical studies from initiation to closure, ensuring timely delivery, within budget and to the required quality standards.This role will involve working cross-functionally with internal and external partners to deliver delegated aspects of the clinical study in accordance with the...

About the RoleWe are seeking an experienced Trial Operations Associate to join our team.In this role, you will be responsible for supporting the management of clinical trials from start-up to close-out.You will work closely with investigators, site staff, and other stakeholders to ensure that trials are managed effectively and efficiently.The ideal candidate...

Role SummaryThis is a full-time position as a Clinical Trials Coordinator, requiring a College/University degree in Life Sciences or an equivalent combination of education, training, and experience. The ideal candidate should have minimum 2 years of experience in independent on-site monitoring in Poland and full working proficiency in Polish, English, and MS...

Job OverviewWe are seeking a highly motivated and detail-oriented Clinical Trial Assistant to join our team at ICON Strategic Solutions. As a key member of our clinical operations team, you will be responsible for providing support to Site Managers (CRA) by distributing and tracking investigator feasibility questionnaires, as well as summarizing results.In...

Job SummaryThis position involves working as a senior-level safety scientist on various clinical trials, ensuring that all aspects of trial operations meet the highest standards. The ideal candidate will have extensive knowledge of clinical trials, data review tools, and regulatory guidelines, as well as excellent analytical and communication skills. This...

OverviewJoin us in redefining what it means to work for a CRO. Dokumeds has become part of Rho, an award-winning, full-service CRO based in North America. As one company, we will deliver global full-service clinical development services and unmatched customer support – worldwide. Working at Rho, you'll be joining a team who take healthcare and clinical...

About the Role:We are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our Clinical Operations team in Poland, Estonia, Lithuania, or Latvia. The successful candidate will have experience in Clinical Trials and possess excellent organizational, communication, and teamwork skills.Key Responsibilities:Preparation of ISFs...

About the Role:The Global Study Manager will be responsible for supporting the delivery of clinical studies within Global Medicines Development (GMD) to time, cost, and quality.This role will involve working cross-functionally with internal and external partners to deliver delegated aspects of the clinical study in accordance with the Global Study Associate...

At Comac Medical, we are seeking a talented Clinical Research Associate to join our team. As a critical member of our clinical research department, you will be responsible for ensuring the success of our clinical trials.Key ResponsibilitiesThe successful candidate will be responsible for developing and maintaining strong relationships with sites...

Job DescriptionClinical Trial Safety Scientist:  Key Responsibilities  Ensure consistent processes and efficient review of critical clinical/safety data.Review patient-level clinical/safety data on an ongoing basis to ensure medical accuracy and completeness, coding consistency, and generate applicable queries as needed for appropriate medical assessment...

Clinical Research OpportunitiesWe are seeking a highly skilled Clinical Research Collaborator to join our team. As a key member of our Clinical Research department, you will play a crucial role in designing and preparing local clinical trials, overseeing their progress, and providing medical reporting.Your primary responsibility will be to collaborate with...

At Indero, we are committed to providing a stimulating work environment that fosters innovation, collaboration, and excellence. We are seeking a highly skilled Clinical Trial Coordinator to join our team in Poland. As a Regulatory Affairs Specialist, you will be responsible for ensuring the quality and compliance of regulatory documents and submissions.\The...

Job TitleClinical Research Associate SMDescriptionThis is an exciting opportunity to join our team as a Clinical Research Associate. The successful candidate will be responsible for performing site monitoring visits, working with sites to adapt and track subject recruitment plans, administering protocol and related study training, and ensuring site documents...