Clinical Research Coordinator

Fortus Healthcare Resources is seeking a Travel Clinical Research Coordinator Non-Clinical for an immediate opening in Sacramento, CA . Clinical, Research, Coordinator, Clinic, Healthcare, Staffing

We are looking for a self-starter to join our team as a Clinical Research Coordinator. We are looking for someone to take ownership of their clinical studies and who can work autonomously to problem solve and stay organized. We are also open to those looking to relocate to California. If you're a Clinical Research professional ready to take the next step in...

We are looking for a self-starter to join our team as a Clinical Research Coordinator. We are looking for someone to take ownership of their clinical studies and who can work autonomously to problem solve and stay organized. We are also open to those looking to relocate to California. If you're a Clinical Research professional ready to take the next step in...

We are looking for a self-starter to join our team as a Clinical Research Coordinator. We are looking for someone to take ownership of their clinical studies and who can work autonomously to problem solve and stay organized. We are also open to those looking to relocate to California. If you're a Clinical Research professional ready to take the next step in...

The Clinical Research Coordinator is primarily responsible for coordinating research patientvisits, and study protocols.Physical Qualifications:Requires prolonged sitting with some standing, some bending, stooping and stretching, hand-eye coordination and manual dexterity to operate keyboard, photocopies, telephone, officeequipment, pertinent clinical...

The Clinical Research Coordinator is primarily responsible for coordinating research patientvisits, and study protocols.Physical Qualifications:Requires prolonged sitting with some standing, some bending, stooping and stretching, hand-eye coordination and manual dexterity to operate keyboard, photocopies, telephone, officeequipment, pertinent clinical...

The Clinical Research Coordinator is primarily responsible for coordinating research patientvisits, and study protocols.Physical Qualifications:Requires prolonged sitting with some standing, some bending, stooping and stretching, hand-eye coordination and manual dexterity to operate keyboard, photocopies, telephone, officeequipment, pertinent clinical...

Responsibilities: Coordinate daily activities for clinical trials and ensure smooth operation. Administer sponsor-required surveys. Collaborate with colleagues to manage study supplies. Train staff on study procedures and keep records of training. Create and maintain trial documents. Attend meetings as requested. Understand and review study protocols. Assist...

Responsibilities: Coordinate daily activities for clinical trials and ensure smooth operation. Administer sponsor-required surveys. Collaborate with colleagues to manage study supplies. Train staff on study procedures and keep records of training. Create and maintain trial documents. Attend meetings as requested. Understand and review study protocols. Assist...

Job Description Come join our team! The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection,...

Job DescriptionResponsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team.Essential Duties And ResponsibilitiesParticipate and assist in design and preparation of protocols and case report forms.Generate clinical SOPs, policies,...

Job Description The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study.  Evaluates and abstracts research data and ensures compliance with protocol and research objectives.  Responsible for completing case report forms, entering...

Job DescriptionJob DescriptionSalary: $45-$65 HourlyJob SummaryThe clinical coordinator(s) must be responsible for coordinating clinical education as assigned by the program director. The clinical coordinator must evaluate and ensure the effectiveness of the clinical affiliate/clinical education centers. The clinical coordinator's responsibilities must...

Job SummaryThe clinical coordinator(s) must be responsible for coordinating clinical education as assigned by the program director. The clinical coordinator must evaluate and ensure the effectiveness of the clinical affiliate/clinical education centers. The clinical coordinator's responsibilities must include coordination, instruction, and evaluation. The...

Job DescriptionJob DescriptionSalary: 38-45Job SummaryThe clinical coordinator(s) must be responsible for coordinating clinical education as assigned by the program director. The clinical coordinator must evaluate and ensure the effectiveness of the clinical affiliate/clinical education centers. The clinical coordinator's responsibilities must include...

Job DescriptionCome join our team!The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection,...

Job Description The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case report forms, entering clinical...

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Position SummaryThe research assistant is primarily responsible for assisting in research patient visits according to ICH-GCPguidelines and according to the IRB-approved study protocol and/or manual of procedures. Day-to-dayactivities may include all or some of the essential functions listed below, depending upon individualexperience / knowledge and the...

Position SummaryThe research assistant is primarily responsible for assisting in research patient visits according to ICH-GCPguidelines and according to the IRB-approved study protocol and/or manual of procedures. Day-to-dayactivities may include all or some of the essential functions listed below, depending upon individualexperience / knowledge and the...