Monitors clinical studies at sites in an assigned territory (and others as requested) to ensure compliance with applicable regulatory requirements, Good Clinical Practice, and accuracy standards inclusive of site initiation, periodic, and close-out visits. Ensures both regulatory and clinical protoc...
Understanding of clinical research activities including tasks associated with study start-up, interim monitoring, closeout, data collection, and central files. Support and/or lead clinical research study start-up activities (including creation of study binders, study logs, work instructions, case re...
Clinical Research Associate (SCRA) on a hybrid capacity in their SF office. Working with a precision IO biotechnology company to build out their clinical operations team and they are currently looking for a Sr. Supporting study operational activities under the direction of the clinical study lead. ...
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...
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...
Job Title: Clinical Research Associate - B. Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Cont...
We are seeking a highly motivated Clinical Research Associate (CRA) to be responsible for supporting the Clinical Development Team to ensure the execution of assigned trials according to the study timelines and company goals and in compliance with ICH GCP, country regulations, and SOPs. Clinical Res...
Job Title: Clinical Research Associate - B. Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Cont...
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, a...
As a vital member of our clinical team, the Clinical Research Associate will be responsible for conducting Phase I-IV single or multi-center studies in adherence to Federal Regulations and ICH guidelines. The ideal candidate should possess a minimum of 2 years of experience in clinical research moni...
You will be working side-by-side with the clinical trial manager and helping oversee the Contract Research Organization. Full time in support of clinical trials for a disease-modifying drug for osteoarthritis. Orthopedic clinical trial experience a "nice to have". ...
Must have a minimum of 2 years experience with "clinical research monitoring". Education: Minimum Associate degree (but prefer Bachelor's) and 2 years of Monitoring experience. ...
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...
Job Title: Clinical Research Associate - B. Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Cont...
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...
The Associate Clinical Research III will assist in the clinical execution and management of all aspects of assigned clinical studies. Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial man...
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...
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...
Job Title: Clinical Research Associate - B. Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Cont...
Supporting study operational activities under the direction of the clinical study lead. ...
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, ...
Responsibilities: As a vital member of our clinical team, the Clinical Research Associate will be responsible for conducting Phase I-IV single or multi-center studies in adherence to Federal Regulations and ICH guidelines. Experience: The ideal candidate should possess a minimum of 2 years of experi...