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Form of workJob Description
We seek a full-time Clinical Research Coordinator II with at least three years of Clinical Research coordinating experience and has been the lead coordinator on five or more research studies. This CRC must also have rater experience.
If you are detail-oriented, self-starter, positive, and prioritize professional working relationships with patients and sponsors, you would be a good fit for our position.
This is an in-person role at our research clinic in Chandler, Arizona. You will be key in conducting and monitoring neurological clinical trials to ensure compliance with procedures and protocols. This will include documenting your findings, recording data, and entering data into electronic data capture systems. Your role is to ensure all aspects of the clinical trials run smoothly and efficiently, ensuring patient safety.
Duties:
Maintains a strong understanding of assigned protocols, protocol requirements for patient visits, obtaining informed consent, patient visit schedules, test procedures, laboratory information, and drug accountability requirements.
Completes all study documentation forms, including case report forms and other study-specific documents.
Coordinates and conducts patient care visits (e.g., drawing blood, collecting vital signs, performing ECGs, processing specimens, shipping laboratory samples) and assures all procedures comply with the study protocol.
Prepares for visits, including monitoring lab supplies, study kits, and patient documents per site procedures.
Interacts with Principal Investigator and Sub-Investigator to ensure the patient receives appropriate medical evaluation and care when needed and alerts Principal Investigator or Sub-Investigator of serious adverse events.
Cultivates close communication with the sponsors Clinical Research Associate to facilitate the sponsor monitoring and database clean-up procedures.
Conducts recruitment calls to potential subjects to gather interest and prescreen for general inclusion/exclusion.
Completes data entry promptly and addresses queries as needed.
Protects confidentiality regarding PHI and other sensitive sponsor information.
Greets and aids visitors, patients, and employees professionally and courteously.
Conforms to site standards of performance and conduct, including those about patient rights, so that the best possible care may be provided.
Requirements:
Minimum requirement: Associate degree in a related field.
Must possess a high degree of integrity and ability to maintain confidentiality with HIPAA guidelines, patient matters, and other sensitive information.
An RN or LPN license or Certification as a Clinical Research Coordinator is a plus.
Strong proficiency in Microsoft Office programs (Outlook, Word) and Web applications.
Laboratory processing experience is preferred.
Phlebotomy skills are preferred.
Psychometric and cognitive assessment experience preferred.
Excellent verbal and written communication skills.
Benefits:
If you are detail-oriented, self-starter, positive, and prioritize professional working relationships with patients and sponsors, you would be a good fit for our position.
This is an in-person role at our research clinic in Chandler, Arizona. You will be key in conducting and monitoring neurological clinical trials to ensure compliance with procedures and protocols. This will include documenting your findings, recording data, and entering data into electronic data capture systems. Your role is to ensure all aspects of the clinical trials run smoothly and efficiently, ensuring patient safety.
Duties:
Maintains a strong understanding of assigned protocols, protocol requirements for patient visits, obtaining informed consent, patient visit schedules, test procedures, laboratory information, and drug accountability requirements.
Completes all study documentation forms, including case report forms and other study-specific documents.
Coordinates and conducts patient care visits (e.g., drawing blood, collecting vital signs, performing ECGs, processing specimens, shipping laboratory samples) and assures all procedures comply with the study protocol.
Prepares for visits, including monitoring lab supplies, study kits, and patient documents per site procedures.
Interacts with Principal Investigator and Sub-Investigator to ensure the patient receives appropriate medical evaluation and care when needed and alerts Principal Investigator or Sub-Investigator of serious adverse events.
Cultivates close communication with the sponsors Clinical Research Associate to facilitate the sponsor monitoring and database clean-up procedures.
Conducts recruitment calls to potential subjects to gather interest and prescreen for general inclusion/exclusion.
Completes data entry promptly and addresses queries as needed.
Protects confidentiality regarding PHI and other sensitive sponsor information.
Greets and aids visitors, patients, and employees professionally and courteously.
Conforms to site standards of performance and conduct, including those about patient rights, so that the best possible care may be provided.
Requirements:
Minimum requirement: Associate degree in a related field.
Must possess a high degree of integrity and ability to maintain confidentiality with HIPAA guidelines, patient matters, and other sensitive information.
An RN or LPN license or Certification as a Clinical Research Coordinator is a plus.
Strong proficiency in Microsoft Office programs (Outlook, Word) and Web applications.
Laboratory processing experience is preferred.
Phlebotomy skills are preferred.
Psychometric and cognitive assessment experience preferred.
Excellent verbal and written communication skills.
Benefits:
- Comprehensive health, dental, and vision insurance
- 401k
- Paid time off and sick time off
- Holidays off
- EAP
