Clinical Research Coordinator
2 weeks ago
We are looking for an experienced CRC to join a multi-site organization in Sacramento, CA. This is a great opportunity to set your roots down with a growing team that offers great benefits and provides a welcoming environment that fosters growth. Apply today
Duties:
- Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study
- Administer sponsor required questionnaires (i.e. VFQ)
- Works with team member responsible for ordering study supplies (lab kits, shippers, etc.) to ensure adequate inventory is on hand
- Ensures study staff is properly trained on study-related information (i.e. protocol, ICF, manuals, etc.) and that the training is documented
- Creates, manages, and maintains source documents for each trial
- Attends teleconferences and Investigator Meetings as requested by research director
- Reviews and comprehends all study protocols, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections
- Works with other members of the study team and clinical team to recruit eligible candidates to meet enrollment goals
- Screens subjects for eligibility using protocol-specific inclusion and exclusion criteria, documenting each potential participant's eligibility accurately
- Efficiently completes all study tasks delegated to them (i.e. scribing, VFQ, IOP, etc.)
- Collects updated medical history, adverse events and serious adverse events that need to be reported to the sponsor and IRB within required time frame
- Conducts and/or participates in the informed consent process/discussion with research participants, including answering any questions related to the study
- Assures that amended consent forms are appropriately implemented and signed
- Acts as a secondary reviewer to provide oversight so that the ICF process is conducted accurately
- Collects data as required by the protocol and enters information into the electronic data capture (EDC) system in the specified timeframe indicated in the study contract.
- Oversees data and ensures that it is being entered correctly and resolves any queries issued within required time frame
- Collects and reports ALL Adverse Events
- Collects and reports ALL Serious Adverse Events
- Responsible for ensuring all SUSAR/Safety Reports are acknowledged and reviewed
- Coordinates monitor site visits and assists with preparation of site visit documentation
- Works with the monitor to make any corrections needed to meet requirements and deadlines as needed
- Manages and maintains all regulatory information about the study including the protocol, investigator brochure, IRB documents, Investigator disclosures, CVs, training documentation, instructions on reporting requirements for the IRB and the sponsor
- Obtain any applicable additional/required sponsor training and/or certifications
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Clinical Research Coordinator
1 month ago
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Clinical Research Coordinator
2 weeks ago
Sacramento, United States Medix Full timeWe 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...
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Clinical Research Coordinator
1 month ago
Sacramento, United States Medix™ Full timeWe 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...
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Clinical Research Coordinator
1 month ago
Sacramento, United States Medix™ Full timeWe 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...
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Clinical Research Coordinator
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Sacramento, United States Medix™ Full timeWe 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...
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Clinical Research Coordinator
4 weeks ago
Sacramento, United States Medix™ Full timeThe 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...
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Clinical Research Coordinator
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Sacramento, United States Medix™ Full timeThe 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...
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Sacramento, United States Medix™ Full timeThe 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...
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Clinical Research Coordinator
2 weeks ago
Sacramento, United States Medix™ Full timeThe 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...
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Clinical Research Coordinator
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Sacramento, United States Medix™ Full timeWe are looking for an experienced CRC to join a multi-site organization in Sacramento, CA. This is a great opportunity to set your roots down with a growing team that offers great benefits and provides a welcoming environment that fosters growth. Apply today!Duties:Facilitates and coordinates the daily clinical trial activities and plays a critical role in...
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Sacramento, United States University of California-Davis Full time#CA-FTThe Assistant Clinical Research Coordinator will support, facilitate and coordinate the daily clinic trial activities for the department research and clinical studies under the direction of the Clinical Research Supervisor. This position will also work with the PIs, other department personnel, and sponsors to support and provide guidance on the...
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Sacramento, United States University of California-Davis Full time#CA-FT The Assistant Clinical Research Coordinator will support, facilitate and coordinate the daily clinic trial activities for the department research and clinical studies under the direction of the Clinical Research Supervisor. This position will also work with the PIs, other department personnel, and sponsors to support and provide guidance on the...
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Sacramento, United States Medix™ Full timeResponsibilities: 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...
