Key Responsibilities:Collaborate with research staff to identify, recruit, and enroll eligible patients for clinical trials virtuallyCollect, maintain, and store all relevant data associated with clinical research trialsInteract with potential participants to educate them regarding clinical research...
The UCLA Center for LGBTQ+ Advocacy, Research, and Health (C-LARAH) is part of the Fielding School of Public Health, within the Department of Epidemiology. The mission of C-LARAH is to maintain an interdisciplinary, research-driven, evidence-based platform used to carry out public policy initiatives...
A company is looking for a Clinical Research Associate on the East Coast. ...
The Clinical Research Coordinator will be the main operational interface with study subjects during the conduct of a clinical trial. Resolves study source document discrepancies including supervising and reviewing completion of documentation of discrepancies by clinical research staff. Schedules and...
Key Responsibilities:Conducting clinical monitoring activitiesEnsuring compliance with protocols, regulatory requirements, SOPs, and monitoring plansParticipating in site feasibility and selectionRequired Qualifications:Bachelor's degree in a scientific discipline or healthcare fieldMinimum of 2 yea...
Spanish and have at least 1-2+ years in clinical research experience. ...
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...
Minimum of [insert number] years of experience in clinical research coordination or related role, preferably in a clinical trial site or research organization. The Clinical Research Coordinator will be responsible for supporting the planning, implementation, and coordination of clinical trials condu...
Spanish and have at least 1-2+ years in clinical research experience. ...
We are a global Clinical Research Institute that has been conducting Clinical Trials over the last 25 years. Clinical Research Coordinator (sponsor-backed trials) Highly Preferred BA/BS in a scientific discipline. We have successfully completed over 1,000 clinical studies together with our primary. ...
The CTRC supports innovative, patient-oriented research, offers clinical research training and recognition programs, and provides researchers with an environment for seeing patients when they take part in clinical research studies. To learn more, please visit Clinical & Translational Research Center...
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...
With minimal supervision, the Clinical Research Coordinator II (CRC-II) is responsible for providing coordinator support to multiple human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities. Association of Clinical Research...
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...
Odyssey Systems Consulting Group, .We focus on people, processes, and performance to deliver superior results.Since our inception in 1997, our commitment to mission success and customer satisfaction has been recognized with exponential growth and exceptional past performance ratings.We accept challe...
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 Data Associate III manages the data for assigned research studies. In addition, may supervise clinical research staff or clinical data managers, perform sophisticated statistical analysis, and work with bioinformatics to develop and maintain trial management and validation syst...
Acquires and utilizes knowledge of clinical trial design to develop specific study concept sheets and protocols. Anticipates moderately complex obstacles within a clinical study and with guidance implements solutions. Excellent verbal and written communication skills and interpersonal skills are req...
The ideal candidate is an experienced professional or leader who has direct responsibility for the implementation of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or progr...
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. ...
Participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support. Bachelors degree with 4+ year experience as a Clinical Trials Asso...
The Clinical Research Coordinator Supervisor (CRC-Su) functions independently and is responsible for the complete coordination of multiple assigned human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities. Association of Cl...
Minimum one (1) year of experience in clinical trials protocols involving research methodology/research study design, and hypothesis testing; OR. If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Minimum one (1) year of training and/or experience in research methodol...
Under moderate supervision, the Clinical Research Coordinator I (CRC-I) is expected to perform all core Clinical Research Coordinator (CRC) responsibilities for human subjects’ (clinical) research. Preferred: Clinical research experience in a hospital setting and/or pediatric clinical research exper...