Clinical Research Coordinator Job at Revival Research Institute, LLC, Elgin, IL

clgwRFZlU1RMalJxLzFMU2VpbWlLS3BwbkE9PQ==
  • Revival Research Institute, LLC
  • Elgin, IL

Job Description

Job Description

Job Description

Unique opportunity to make an Impact in the healthcare industry…  

Revival Research Institute, LLC was established in 2015, and headquartered in the Metro Detroit Region, and has been growing ever since. Revival now has a national presence in the  Metro-Detroit Region, Texas, Illinois, and Arizona. We have been nationally acknowledged for our diligence to provide the highest quality of data for our clinical research trials.

As  Revival Research Institute is growing, we are looking to add more qualified professionals to our team, who are looking for an opportunity to grow and learn with us.

We are seeking a full-time  Clinical Research Coordinator with a minimum of 1 year of clinical experience, for our Additionally, someone with a strong interest in the Clinical Research field would be an excellent fit for our entry level position, with room to grow. However, this interest and background is not necessary, as our ideal candidate is an individual who is detail orientated, being able to maintain organized records, as well as someone who is motivated to learn new things, as our company is always growing and expanding into new therapeutic areas. We are looking for individuals that want the opportunity to learn and grow with us.

Clinical Research Coordinators here at  Revival Research Institute , should be genuinely respectful of diverse points-of-view and strive for an environment in which inclusiveness drives productivity and results. Clinical Research Coordinators are responsible to coordinate and manage multiple studies. They are also responsible for assisting the Investigators along with other clinical staff, with any study related tasks as follows but not limited to: 

  1. Participates in research participant screening, recruitment and enrollment. Consent and conduct research visits for data collection/no risk trials or no study article/minimal risk trials with oversight. Responsible for collecting, processing and shipping of research specimens, where applicable. 

  2. Documents study related information in case report forms or electronic data capture systems, handles data queries and participates in monitoring visits. Obtain, review and maintain source documents. 

  3. Maintains organization of all trial related documents and correspondence. Implement quality control and assurance methods. 

  4. Communicate with study sponsors, research team and the Institutional Review Board. Assist with basic regulatory document preparation, with oversight e.g. study amendments, adverse event reporting, protocol deviation reporting. 

  5. Maintain professional and technical knowledge about Clinical trials. 

  6. Research participant/family communication, protect patient confidentiality. 

Preferred Qualifications: 

  1. Education/ Training: Bachelor's degree in health-related field with one to two years relevant clinical experience OR Master's degree in medical related field with no research experience. Individuals with more experience are preferred, if qualifications exceed entry level, higher positions available. 

  2. Phlebotomy skills preferred. 

  3. Psychology experienced with knowledge regarding the psychiatric rating scale is preferred.

  4. Certifications, Licensures, and Registrations: National Certification (CRA or ACRP), BLS Certification.

  5. Additional Qualifications: Expert database and computer skills: Microsoft Office (Word, Excel), Outlook, excellent verbal and written communication skills, ability to work independently and assume responsibility, excellent organizational skills, ability to meet data deadlines and maintain confidentiality. Maintain data integrity within the department. Must be able to work in a team consisting of physicians, nurses, technicians, secretarial staff and ancillary hospital staff. Knowledge of FDA Regulations and Good Clinical Practices. 

IMPROVE THE FUTURE AS OUR CLINICAL RESEARCH COORDINATOR!!! 

Powered by JazzHR

TLki8ovEMq

Job Tags

Full time,

Similar Jobs

DenkenSolutions Inc

Data Analyst - Workday Job at DenkenSolutions Inc

 ...interested please reply to me with your updated resume or feel free to reach out to me for more details at(***) ***-**** Data Analyst - Workday Location: Irving, TX Duration: 6 Months Contract Responsibilities: Run ad-hoc analysis to analyze and... 

Sanford Health

Respiratory Therapist - Bemidji Medical Center - Full Time Straight Nights Job at Sanford Health

 ...nearly 50,000 members of the Sanford Family who are dedicated to the work of health and healing across our broad footprint....  ...benefits, and a generous time off package to maintain a healthy home-work balance. For more information about Total Rewards, visit .... 

Fidelity Investments

Entry Level Customer Service - Merrimack, NH Job at Fidelity Investments

 ...Description: Join our team of Customer Relationship Advocates (CRA)...  ...and learn what it is like to work in this role. This is free for...  ...develop the skills needed to service customers and study for your FINRA...  ...in the office, working from home, overtime, etc.) Ability to... 

H.J. Martin and Son

Residential Flooring Installer Job at H.J. Martin and Son

Green Bay, WIResidential Flooring InstallerPosted on November 7, 2023Job ID: 1699383991Hours: Full-time; 40 or more hours per...  ...~Install LVT & LVP, VCT, carpet, sheet vinyl, wood, laminate, tile, and other specified flooring~Cut floor coverings and foundation... 

Home Buyers Realty

Agente de Bienes Raices Job at Home Buyers Realty

 ...la colaboracin y el apoyo entre colegas sea la norma. Cada miembro de nuestro equipo es valorado, y juntos, creamos una cultura de trabajo positiva y motivadora. Oportunidades de Capacitacin y Desarrollo Continuo: Te mantenemos a la vanguardia del sector con...