Join Our Dynamic Clinical Research Team in Redmond!
Behavioral Health Market Context
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Job Description
ory standards.
A valid and current Registered Nurse (RN) license in the State of Washington is a mandatory requirement for this position. Applications without a Washington RN license will not be considered.
DUTIES & RESPONSIBILITIES
Responsibilities:
- Assist with patient screening and recruitment for clinical trials.
- Support the informed consent process under the direct supervision of a senior CRC or manager.
- Perform basic clinical data entry and management into -Electronic Data Capture (EDC) systems.
- Assist with scheduling patient visits and procedures.
- Help with the preparation of source documents and study binders.
- Maintain inventory of study supplies and equipment.
- Handle processing and shipment of lab samples following IATA/DOT regulations (with training).
- Attend study meetings and complete required training (GCP, HIPAA, Protocol-specific).
- Perform nursing assessments and conduct protocol-related procedures (vitals, ECGs, infusions, pharmacokinetic sampling, etc.).
- Administer investigational products (drugs, devices, biologics) per protocol.
- Monitor patient responses to investigational products and provide clinical care.
- Assess, document, and report Adverse Events (AEs) and Serious Adverse Events (SAEs) to the PI and sponsor.
- Provide patient education and serve as a clinical resource for participants throughout the study.
- In addition to the specific responsibilities outlined above, this role may perform other tasks or projects as assigned by a supervisor or manager. These additional duties will fall within the scope of the role and contribute to the overall success of the team.
A valid and current Registered Nurse (RN) license in the State of Washington is a mandatory requirement for this position. Applications without a Washington RN license will not be considered.
DUTIES & RESPONSIBILITIES
Responsibilities:
- Assist with patient screening and recruitment for clinical trials.
- Support the informed consent process under the direct supervision of a senior CRC or manager.
- Perform basic clinical data entry and management into -Electronic Data Capture (EDC) systems.
- Assist with scheduling patient visits and procedures.
- Help with the preparation of source documents and study binders.
- Maintain inventory of study supplies and equipment.
- Handle processing and shipment of lab samples following IATA/DOT regulations (with training).
- Attend study meetings and complete required training (GCP, HIPAA, Protocol-specific).
- Perform nursing assessments and conduct protocol-related procedures (vitals, ECGs, infusions, pharmacokinetic sampling, etc.).
- Administer investigational products (drugs, devices, biologics) per protocol.
- Monitor patient responses to investigational products and provide clinical care.
- Assess, document, and report Adverse Events (AEs) and Serious Adverse Events (SAEs) to the PI and sponsor.
- Provide patient education and serve as a clinical resource for participants throughout the study.
- In addition to the specific responsibilities outlined above, this role may perform other tasks or projects as assigned by a supervisor or manager. These additional duties will fall within the scope of the role and contribute to the overall success of the team.
Qualifications
- •A valid and current Registered Nurse (RN) license in the State of Washington is a mandatory requirement for this position
- •Applications without a Washington RN license will not be considered
Benefits
Responsibilities
- •This role is an entry-level role focused on learning the fundamental principles of clinical research coordination under close supervision
- •This individual supports the research team by performing routine data collection and administrative tasks, ensuring compliance with protocols and regulatory standards
- •Assist with patient screening and recruitment for clinical trials
- •Support the informed consent process under the direct supervision of a senior CRC or manager
- •Perform basic clinical data entry and management into -Electronic Data Capture (EDC) systems
- •Assist with scheduling patient visits and procedures
- •Help with the preparation of source documents and study binders
- •Maintain inventory of study supplies and equipment
- •Handle processing and shipment of lab samples following IATA/DOT regulations (with training)
- •Attend study meetings and complete required training (GCP, HIPAA, Protocol-specific)
- •Perform nursing assessments and conduct protocol-related procedures (vitals, ECGs, infusions, pharmacokinetic sampling, etc.)
- •Administer investigational products (drugs, devices, biologics) per protocol
- •Monitor patient responses to investigational products and provide clinical care
- •Assess, document, and report Adverse Events (AEs) and Serious Adverse Events (SAEs) to the PI and sponsor
- •Provide patient education and serve as a clinical resource for participants throughout the study
- •In addition to the specific responsibilities outlined above, this role may perform other tasks or projects as assigned by a supervisor or manager
- •These additional duties will fall within the scope of the role and contribute to the overall success of the team
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