Clinical Research Professional

Job OverviewWe are seeking an experienced Clinical Research Associate to join our team at August Research. As a key member of our clinical research team, you will be responsible for site identification and selection, regulatory submissions, monitoring for clinical studies, and local safety reporting.This is a full-time position for candidates with at least...

Job OverviewCare Access Research is a unique multi-specialty network of research sites operating as one connected team of physician investigators, nurse coordinators, and operations managers. Our mission is to engage every healthcare professional in clinical research and make clinical trials a care option for every patient.Key ResponsibilitiesSupporting the...

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...

Job DescriptionWe are seeking an experienced Clinical Research Associate to join our team at August Research. The successful candidate will be responsible for:Site identification and selectionRegulatory submissionsMonitoring for clinical studiesLocal safety reportingThis is a full-time position for candidates with at least one year of monitoring experience....

Job DescriptionAt TN Poland, we are seeking a highly skilled Clinical Research Professional to join our international team. As a Senior Clinical Trial Specialist, you will play a crucial role in providing feasibility services, contributing to business development, and ensuring the smooth conduct of newly awarded trials.This is an excellent opportunity for...

Key ResponsibilitiesThe Clinical Research Associate will be responsible for:Identifying and selecting suitable sites for clinical studiesMaintaining accurate and detailed records of study activitiesEnsuring compliance with regulatory requirements and company policiesCommunicating effectively with internal stakeholders and external partnersRequirements and...

Comac Medical seeks a highly skilled Clinical Research Associate to join our team. As a key member of our clinical research department, you will play a critical role in ensuring the success of our clinical trials.About the RoleThe primary responsibility of this position is to develop and maintain strong relationships with sites participating in our clinical...

Job Title: Clinical Research AssociateAbout the Role:We are seeking a highly motivated and detail-oriented Clinical Research Associate to join our team at IQVIA Argentina. As a CRA, you will be responsible for monitoring and managing clinical trials, ensuring compliance with regulatory requirements and sponsor expectations.Key Responsibilities:Perform site...

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...

Clinical Programming RoleWe are looking for an experienced Clinical Programmer to join our team. The ideal candidate will have a strong background in programming in relational database settings using SQL and/or T-SQL or ETL, as well as experience with data reporting tools in a clinical trial setting.The selected candidate will contribute to the development...

As a Clinical Research Expert at TN Poland, you will be responsible for providing expert guidance on regulatory matters and ensuring compliance with complex regulatory issues and projects.Responsibilities:Conduct regulatory intelligence gathering to support development of regulatory roadmaps.Author and maintain documentation to sustain regulatory...

We are committed to helping change lives through our innovative approaches to cancer prevention, detection, and treatment. As a Clinical Research Advocate, you will play a crucial role in educating healthcare providers and patients about our products and services.You will be responsible for developing and executing outreach plans, mapping key accounts and...

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 Title: Clinical Research AssociateClinical Research Associate will verify the accuracy and completeness of trial data, protect human subjects' rights and well-being, and ensure conduct follows approved protocol, GCP, and local legislations.Key Responsibilities:Perform site selection, initiation, and closing activities in compliance with regulations,...

What is expected to be done?Conducts feasibility studies and site qualification visits;Develops and ensures a strong site relationship through all phases of the trial;Gains in-depth understanding of the study protocol and related procedures;Prepares study documentation eg draft protocols, draft CRFs;Collects, reviews, and monitors required regulatory...

Company OverviewPSI CRO AG is a global contract research organization committed to improving patients' lives through clinical studies. With offices across six continents, our team members enjoy autonomy in making decisions and creating an engaging work environment.

About Clinical ResearchClinical research plays a vital role in advancing medical breakthroughs and bringing life-changing therapies to patients. At Care Access, we unite standard patient care with cutting-edge treatments and research, paving the way for newer and greater treatments to reach the world.The Role of Operational Compliance AssociateThis position...

OverviewIQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry.Job DescriptionWe are seeking a highly skilled Clinical Research Associate to join our team. The successful candidate will be responsible for performing site monitoring visits, working with sites to adapt and...

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...

About the RoleKey AccountabilitiesDevelop and execute global contracting strategies to support business development and clinical trial initiation.Lead cross-functional teams to ensure effective execution of contracting activities.Maintain and develop strong relationships with sponsors, stakeholders, and internal teams.Ensure compliance with sponsor...