beBeeClinicalResearchAssociate Jobs in United States

Key Responsibilities of Clinical Research Associate II · The Clinical Research Associate II plays a pivotal role in the success of clinical trials. Key responsibilities include: · Designing and implementing clinical protocols and case report forms. · Developing and managing clini ...

Key Responsibilities · The onsite Monitoring Specialist will be responsible for: · Monitoring and evaluating the quality of study site practices · Evaluating and resolving quality issues as needed · Managing project expectations and tracking regulatory submissions and approvals · ...

Senior Clinical Research Associate Job Description · We are seeking a dedicated Clinical Research Associate to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and managing clinical ...

Job Role: · Clinical Research Associates drive the success of clinical trials by ensuring high-quality, compliant data collection and analysis. · The primary duties of a Clinical Research Associate involve: · Conducting site qualification and initiation visits to ensure trial sit ...

Clinical Research Associate 2 Job Overview · We are seeking a Clinical Research Associate 2 with on-site monitoring experience in GLP-1/Obesity/Diabetes or Cardiovascular clinical trials to join our team. Phase 1 experience is highly desirable. · ...

Job Description · As a key member of our team, you will be responsible for project activities associated with monitoring functions of phase I through phase IV clinical research studies and Real World Evidence (RWE) studies. You will develop knowledge of the drug development proce ...

Clinical Research Associate II Job Description · This position serves as a vital member of the clinical study team, providing comprehensive support for all clinical trials. · Under the direction of a supervisor or designee, this role will assist in designing and preparing protoco ...

The ideal candidate will have excellent communication and interpersonal skills, with the ability to build strong relationships with sites and colleagues. · Requirements · Bachelor's degree in a life science or healthcare-related field. · Minimum 1.5 years of on-site oncology moni ...

Job Description · This role involves performing site qualification, initiation, interim monitoring, site management activities and close-out visits to ensure regulatory compliance. The candidate will evaluate site performance, communicate with project teams, and maintain knowledg ...

Clinical Research Associate · The role involves conducting site monitoring responsibilities for clinical trials with a high level of independence. · Qualify, initiate, conduct interim and close-out visits to ensure proper documentation. · Prepare accurate and timely visit reports ...

Job Title: Clinical Research Associate · We are seeking a highly skilled Clinical Research Associate with 1.5 years of on-site oncology monitoring experience to join our team. · About the Role: · Perform site monitoring visits in accordance with contracted scope and regulatory re ...

Clinical Research Associate Role Overview · The Clinical Research Associate will play a pivotal role in the execution of clinical trials, ensuring compliance with study protocols and regulatory requirements. Key responsibilities include monitoring and managing clinical sites, con ...

Clinical Research Associate Role · Design and implement clinical trials, interpreting complex medical data to contribute to innovative treatments and therapies. Key responsibilities include conducting site qualification visits, ensuring protocol compliance, collaborating with inv ...

Clinical research associates are crucial to the execution of successful clinical trials. We are looking for a motivated individual to conduct site visits, monitor compliance, and manage expectations. · This role requires strong analytical skills to assess site performance, escala ...

Clinical Trial Execution and Compliance · The ideal candidate for this Clinical Research Associate role will have a minimum of 1 year of on-site monitoring experience and a strong understanding of GCP and ICH guidelines. · Key responsibilities will include: · Conducting site visi ...

Job Title: Clinical Research AssociateWe are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a critical role in ensuring the success of our clinical studies by conducting site monitoring visits, working with s ...

Clinical Research Associate Role Overview · Our team is seeking a dedicated Clinical Research Associate to execute clinical trials successfully. · Conduct site visits to implement effective recruitment strategies, monitor progress, and resolve issues. · Collaborate with site staf ...

Clinical Research Associate Role Description · This position is responsible for ensuring the quality and integrity of clinical research and clinical trial sites through on-site assessments and assistance with clinical research efforts. · The ideal candidate will have a strong und ...

Role Summary: · We are looking for a highly skilled Clinical Research Associate II to join our team. As a key member of the clinical study team, you will provide support for all clinical trials, working under the direction of a supervisor or designee. · Main Responsibilities: · D ...

Remote Clinical Research Associate Role · Omni-Inclusive is seeking a highly skilled Clinical Research Associate to join our Clinical Affairs Department. As a key member of our team, you will play a vital role in supporting clinical activities to generate evidence for product reg ...