Clinical Research Associate (CRA/Senior CRA for In-House Opportunity). Participate in providing guidelines for assessing the adequacy of potential clinical investigators and sites: including evaluating facilities, personnel, patient referral base, and adherence to Good Clinical Practices (GCP). Part...
Clinical Research Associate (Part-Time). Collaborate with Contract Research Organizations (CROs) and vendors to ensure efficient delivery of study materials and documentation to investigator sites. Minimum of 2+ years of clinical monitoring experience in oncology trials required. ...
Reporting to the Lead Clinical Research Associate, the CRA II/Sr. This role will collaborate closely with key cross-functional internal stakeholders including Clinical Operations, Medical Monitoring, Data Management, Supply Chain, and Clinical Compliance and Quality as well as external CRO and vendo...
The Senior Clinical Research Associate will report to Manager, Clinical Affairs, and will play a key role to proactively support the conduct of pre-market and post-market clinical studies to ensure compliance with all the regulatory requirements. Contribute to all clinical research activities to ens...
As the Clinical Research Associate, you will independently monitor clinical trial data by Good Clinical Practices (GCP), ICH, FDA, and internal standard operating procedures (SOPs). Thorough knowledge of clinical research concepts, practices, GCDMP, FDA regulations, and ICH Guidelines regarding drug...
Responsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions. Under the direction of supervisor or designee, this position will serve ...
CLINICAL TRIALS:Responsible for assisting in the selection and administration of appropriate clinical research trials by reviewing studies, adhering to federal regulations and ICH Guidelines, with an emphasis on good clinical practice and clinical Safety Data Management. Under direction of the Manag...
Under direction of the Manager of Grants & Special Projects, the Clinical Research Associate coordinates all aspects of clinical trials within the assigned unit. Responsible for assisting in the selection and administration of appropriate clinical research trials by reviewing studies, adhering to fe...
The Clinical Research Associate position is responsible to support and execute clinical project plans to identify and complete clinical trial milestones with accountability for successful completion of all project deliverables for clinical trials in accordance with GCP, all applicable regulations, ...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery at sites within established protocols and portfolio under gene...
The Clinical Research Associate I (CRAI) will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study. This role is responsible for completing case report forms (CRFs) and entering clinical...
Excellentknowledge of Clinical Research methods andprocedures. Scor other diploma from a Clinical Researchprogram. Avalid Clinical Researchlicense. Yourexpertise and opinions shall be valuable to us which shall help usin ourresearch. ...
The Clinical Research Associate I (CRAI) will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study. This role is responsible for completing case report forms (CRFs) and entering clinical...
Supporting study operational activities under the direction of the clinical study lead. ...
The Clinical Research Associate I (CRAI) will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study. This role is responsible for completing case report forms (CRFs) and entering clinical...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data analysis; and data reporting and interpretation. The Senior CRA will assist in the clinical execution and manage...
Under the supervision of Principal Investigator (PI), the clinical research coordinator (CRC) will perform duties related to the support and coordination of clinical research studies and may receive training and development to prepare and advance for journey-level work at the next level within the s...
The Clinical Research Associate is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out. The Clinical Research Associate will oversee the conduct of the trial at designated sites, ensuring the rights and well-be...
The Clinical Research Coordinator will plan, direct, or coordinate clinical research projects, and will evaluate and analyze clinical data. Works with PI, co-investigators and trainees on the research team to facilitate completion of research proposals, projects, manuscripts, abstracts and presentat...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...