Qureos Mentor

Panoramic Health

Advancing Care Through Innovation
 Position is on-site Monday - Friday in Providence, RI
 Nephrology Associates Inc 314 Taunton Ave, East Providence, RI 02914
 
To learn more about Panoramic Science visit: https://panoramichealth.com/clinical-research/
 
Come Join Panoramic's Science Divison!
 
The Clinical Research Coordinator II leads the clinical research program at the site level: effectively recruiting and enrolling research patients under the clinical direction of the principal investigator, and always in compliance with institutional Standard Operating Procedures, protocol specifications, and good clinical practice. In addition, proactively develops an implements workflows to optimize recruitment, enrollment, and study execution.
 
Responsibilities: 
<ul>
<li>Read and understand assigned research protocols. Prescreen patients. Train site staff on study purpose, record attendance. Evaluate resources needed and on-hand to appropriately deploy the study</li>
<li>Proactively recruit potentially eligible patients for research studies by communicating eligibility criteria and flagging potentially eligible patients to referring physicians and clinic staff. Work collaboratively with clinic leadership and staff to identify and implement effective processes for communicating study opportunities to patients and providers. Work collaboratively with central Research departments, including Central Enrollment Team, to meet and exceed targets for referrals, consents and enrolled patients. Obtain and document informed consent per ICH/GCP and site SOPs. Timely, clean data entry according to ALCOA principle (“Attributable, Legible, Contemporaneous, Original and Accurate”)</li>
<li>Prepare for monitoring visits:</li>
<li>All Source Documents organized and readily available.</li>
<li>Responds in a timeline fashion to monitor letters assuring all outstanding items from prior monitoring visit are resolved.</li>
<li>No open queries from prior visit.</li>
<li>Temperature and accountability logs are kept current and readily available.</li>
<li>Ongoing Study oversight and management:</li>
<li>Plan subject visits according to protocol specific visit schedule. No protocol deviations due to out of window procedures.</li>
<li>Communication with location administration to make sure space and other resources are available as needed.</li>
<li>Reporting of Adverse and Serious Adverse Events to IRB, Sponsor and management in accordance with reporting guidelines.</li>
<li>Dispensing/collecting study medication and providing accurate Investigational Product accountability.</li>
<li>Collecting and processing subject laboratory specimens according to protocol.</li>
<li>Completing case report forms (CRFs) and other patient tracking information (either electronic or manual) accurately and on a timely basis as assigned.</li>
<li>Maintaining a thorough understanding of all data collection instruments and collecting data accurately and according to protocol</li>
<li>Communication with location administration to make sure space and other resources are available as needed</li>
<li>Reporting of Adverse Events to IRB, Sponsor and management in accordance with reporting guidelines</li>
<li>Dispensing and collecting medication and providing accurate Investigational Product accountability</li>
<li>Collecting and processing subject laboratory specimens according to protocol.</li>
<li>Completing case report forms (CRFs) and other patient tracking information (either electronic or manual) accurately and on a timely basis as assigned.</li>
<li>Maintaining a thorough understanding of all data collection instruments and collecting data accurately and according to protocol.</li>
<li>Perform other duties and responsibilities as required, assigned, or requested</li>
</ul>
Qualifications: 
<ul>
<li>MA Certification preferred</li>
<li>Bachelor’s degree in health-related field preferred</li>
<li>Good Clinical Practice and or ITIA Certification preferred</li>
<li>ACRP or Socra Certification preferred</li>
<li>Bilingual preferred (Spanish)</li>
<li>Minimum 3 year’s to 5 year’ss clinical research experience</li>
<li>Therapeutic area experience in CKD, nephrology, or vascular access a plus.</li>
<li>Must have knowledge of medical terminology/ research</li>
<li>Self-motivated individual who will drive patient safety, achievement of enrollment targets, quality timely data entry, and adherence to Good Clinical Practice (GCP).</li>
<li>Requires excellent interpersonal and communication skills.</li>
<li>Requires flexibility, excellent organizational/communication skills, and attention to detail.</li>
<li>Knowledge of and adherence to Good Clinical Practice (GCP), IATA and FDA regulations.</li>
<li>Must be able to do basic clinical procedures such as: blood work, vitals, height, weight, etc.</li>
<li>Must be able to do an ECG.</li>
<li>Must be able to multitask, able to handle a high volume of patients across multiple studies.</li>
<li>Open to working a flexible schedule.</li>
</ul>
The Company is committed to the principles of equal employment. We are committed to complying with all federal, state, and local laws providing equal employment opportunities, and all other employment laws and regulations. It is our intent to maintain a work environment which is free of harassment, discrimination, or retaliation because of age, race, color, national origin, ancestry, religion, sex, pregnancy (including childbirth, lactation and related medical conditions), physical or mental disability, genetic information (including testing and characteristics), veteran status, uniformed servicemember status, or any other status protected by federal, state, or local laws. The company is dedicated to the fulfillment of this policy in regard to all aspects of employment, including but not limited to recruiting, hiring, placement, transfer, training, promotion, rates of pay, and other compensation, termination, and all other terms, conditions, and privileges of employment
 
For information about our Privacy Policy, please visit here

Research | Clinical Research Coordinator II | Providence, Rhode Island

Advancing Care Through Innovation
 Position is on-site Monday - Friday in Ft. Worth, TX
 North Texas Kidney Associates - NTKDA 6331 Boulevard 26, #220, North Richland Hills TX 76180
 <ul>
<li>Position requires Phlebotomy Experience</li>
</ul>
To learn more about Panoramic Science visit: https://panoramichealth.com/clinical-research/
 
Come Join Panoramic's Science Divison!
 
Clinical Research Coordinator I will perform delegated duties such as protocol required visit procedures, administering questionnaires and subject material, administering, and dispensing medication, adhering to regulatory guidelines, and participating in subject recruitment efforts, under the oversight of the study Principal Investigator. The Clinical Research Coordinator needs to engage with the Principal Investigators, pharmaceutical companies (Sponsors) and contract research organizations (monitors) as well as the research subjects.
 
Responsibilities include: 
<ul>
<li>Read and understand assigned research protocols. Prescreen patients. Train site staff on study purpose, record attendance. Evaluate resources needed and on-hand to appropriately deploy the study.</li>
<li>Drive enrollment to meet contractual targets: Using the EMR, screen for eligible patients for discussion and qualification by the Principal Investigator. Obtain and document informed consent per ICH/GCP and site SOPs. Timely, clean data entry according to ALCOA principle (“Attributable, Legible, Contemporaneous, Original and Accurate”).</li>
<li>Prepare for monitoring visits: All Source Documents organized and readily available. All outstanding items from prior monitoring visit are resolved. No open queries from prior visit. Temperature and accountability logs readily available.</li>
<li>Ongoing Study oversight and management: Plan subject visits according to protocol specific visit schedule. No protocol deviations due to out of window procedures. Communication with location administration to make sure space and other resources are available as needed. Reporting of Adverse and Serious Adverse Events to IRB and Sponsor in accordance with reporting guidelines. Dispensing/collecting study medication and providing accurate Investigational Product accountability. Collecting and processing subject laboratory specimens according to protocol. Completing case report forms (CRFs) and other patient tracking information (either electronic or manual) accurately and on a timely basis as assigned. Maintaining a thorough understanding of all data collection instruments and collecting data accurately and according to protocol.</li>
<li>Perform other duties and responsibilities as required, assigned, or requested.</li>
</ul>
Qualifications: 
<ul>
<li>Bachelors’ degree required; Nursing or Health Science preferred.</li>
<li>Bilingual preferred (Spanish).</li>
<li>Minimum 2 years’ experience as a clinical research coordinator.</li>
<li>Therapeutic area experience in CKD, nephrology, or vascular access a plus.</li>
<li>Knowledge of and adherence to Good Clinical Practice (GCP), IATA and FDA regulations.</li>
<li>Must be able to do basic clinical procedures such as: blood work, vitals, height, weight, etc.</li>
<li>Must be able to do an ECG.</li>
<li>Travel to Investigator meetings or other study locations is expected with this position. Travel might be outside the local area and overnight.</li>
</ul>
The Company is committed to the principles of equal employment. We are committed to complying with all federal, state, and local laws providing equal employment opportunities, and all other employment laws and regulations. It is our intent to maintain a work environment which is free of harassment, discrimination, or retaliation because of age, race, color, national origin, ancestry, religion, sex, pregnancy (including childbirth, lactation and related medical conditions), physical or mental disability, genetic information (including testing and characteristics), veteran status, uniformed servicemember status, or any other status protected by federal, state, or local laws. The company is dedicated to the fulfillment of this policy in regard to all aspects of employment, including but not limited to recruiting, hiring, placement, transfer, training, promotion, rates of pay, and other compensation, termination, and all other terms, conditions, and privileges of employment
 
For information about our Privacy Policy, please visit here

Clinical Research Coordinator in Ft. Worth, Texas

Join Panoramic Health and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Panoramic Health

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Research | Clinical Research Coordinator II | Providence, Rhode Island

Clinical Research Coordinator in Ft. Worth, Texas