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Clinical Research Rater Remote Jobs in Kansas (NOW HIRING)

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Clinical Research Associate II

Lenexa, KS · Remote

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

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Clinical Research Associate II

Lawrence, KS · Remote

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

Syneoshealth

Our Clinical Solutions team members act with a drug development mindset, applying their years of ... US or Canada (Hybrid/Remote) Position Overview The Research Associate/Senior Research Associate ...

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CRA II and Senior CRA

Lawrence, KS · Remote

$91K - $114K/yr

S.) ICON is a global healthcare intelligence and clinical research organisation united by a mission ... MM2 #LI-Remote Employment with ICON is contingent upon having the legal right to work in the ...

410 ICR United States USA

CRA II

Lawrence, KS · Remote

$91K - $114K/yr

CRA II (Home-based in U.S.) ICON is a global healthcare intelligence and clinical research ... MM2 #LI-Remote Employment with ICON is contingent upon having the legal right to work in the ...

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Clinical Research Rater Remote information

What is a clinical research rater?

A Clinical Research Rater (Remote) is a professional who works from a remote location to assess and evaluate participants in clinical research studies. They are responsible for administering psychological or cognitive assessments, interviews, and questionnaires to study subjects according to research protocols. The data they collect is used to determine the effectiveness and safety of medical treatments or interventions being studied. This position requires strong attention to detail, excellent communication skills, and the ability to follow standardized procedures. Remote raters typically collaborate with research teams via secure digital platforms and may require specific certifications or training.

What are the key skills and qualifications needed to thrive as a clinical research rater?

To thrive as a Clinical Research Rater (Remote), you need a background in psychology, neuroscience, or a related field, along with experience in clinical research and administering standardized assessments. Familiarity with electronic data capture (EDC) systems, clinical trial protocols, and certifications such as Good Clinical Practice (GCP) are highly valued. Attention to detail, strong organizational skills, and the ability to communicate clearly with research teams are crucial soft skills. These abilities ensure accurate data collection, adherence to study protocols, and high-quality research outcomes in a remote environment.

What are some typical challenges faced by remote clinical research raters, and how can they be addressed?

Remote Clinical Research Raters often face challenges such as maintaining consistent communication with study teams and ensuring accurate, unbiased assessments when working independently. To address these, it's important to establish clear protocols for virtual collaboration, regularly attend team meetings, and utilize secure data management systems. Staying organized and proactively reaching out for clarification when needed can help maintain high-quality data collection and foster a supportive remote work environment.

What is the difference between Clinical Research Rater Remote vs Clinical Data Entry Specialist?

AspectClinical Research Rater RemoteClinical Data Entry Specialist
Required credentialsHigh school diploma or equivalent; some roles may require clinical or research experienceHigh school diploma or equivalent; data entry skills preferred
Work environmentRemote, flexible hours, often part-timeRemote or on-site, regular hours, often full-time
Employer and industry usagePharmaceutical companies, research organizations, clinical trial sitesHealthcare providers, research organizations, hospitals

While both roles involve working remotely in the healthcare and research industry, Clinical Research Rater Remote focuses on evaluating patient data and clinical outcomes, whereas Clinical Data Entry Specialists primarily input and manage clinical data. The roles differ in responsibilities, with the former emphasizing assessment and analysis, and the latter concentrating on data accuracy and entry.

What are the most commonly searched types of Clinical Research Rater jobs in Kansas?

The most popular types of Clinical Research Rater jobs in Kansas are:

What are popular job titles related to Clinical Research Rater Remote jobs in Kansas?

For Clinical Research Rater Remote jobs in Kansas, the most frequently searched job titles are:

What job categories do people searching Clinical Research Rater Remote jobs in Kansas look for?

The top searched job categories for Clinical Research Rater Remote jobs in Kansas are:

What cities in Kansas are hiring for Clinical Research Rater Remote jobs?

Cities in Kansas with the most Clinical Research Rater Remote job openings:

Clinical Research Rater Remote jobs near you

Home Health Nurse (Clinical Research)

Manhattan, KS • On-site, Remote

Medical Research Network
Offices of Mental Health Practitioners • 1 - 10 employees
Learn more about Medical Research Networkexternal

Part-time

Re-posted 10 days ago

Job description

Company Description
The Medical Research Network is the leader in the innovative field of providing clinical trial treatment in a patient's home. We work with nurses across the US to administer study drugs, collect safety bloods and conduct other clinical activities. You will be working on ground breaking clinical trials, which can provide new and improved treatments.
Job Description
This is an excellent opportunity for an experienced Pediatric or Adult Nurse to join a unique organization and positively impact patients' quality of life, increasing patient recruitment and retention into clinical trials.
MRN offers home visits for patients on a per diem basis whereby the schedules are determined by the clinical trial protocol (for example; weekly, or monthly visits). Patients are referred, and the nurses are allocated to complete visits generally within a one-hour travel distance.
MRN works on clinical trials across the world and we require nurses with excellent clinical skills to join our team working at the forefront of clinical research.
Qualifications
Do you have the following skills and experience?
  • Registered Nurse license
  • At least 2 years' post registration experience required, with some community / home health care experience preferred
  • Experience in Clinical Research desirable with knowledge of GCP (Good Clinical Practice) desirable (not required as training will be given)
  • Experience as a Research Nurse is highly desirable
  • Experience in administration of intravenous therapies (Mandatory)
  • Cannulation and phlebotomy skills (Mandatory)
  • Experience in using Central Venous access Devices (Highly Desirable)
  • Enthusiastic, positive attitude with great attention to detail
  • Great organizational skills and ability to plan visit activities independently
  • Excellent communication skills and the ability to complete complex data requirements

Please note, you will be required to travel so a drivers licence and access to a vehicle is essential!
In return we can offer you:
  • Excellent rates of pay (including visits, training time and travel time)
  • Per diem schedule - variety of shifts available from mornings to evenings, dependent upon specific patient needs
  • Paid travel time and mileage reimbursement
  • Paid training on research studies - including GCP (Good Clinical Practice) training and certification
  • Opportunity to be a part of ground-breaking clinical trial research
  • Direct deposit
  • Referral Program

If you feel you have the skills, experience and attitude to be a success, then please Apply Today for immediate consideration!
Data Protection - Your Rights
Should you apply for a job opportunity at The MRN, we wish to inform you that it is our intention to retain the personal data provided by you for up to 2 years from the date it is received, at which point you will be asked to provide new consent. If you have any questions or concerns regarding our processes and how your personal data will be stored, please contact us for further reassurance.
Additional Information
All your information will be kept confidential according to EEO guidelines.

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