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Program

Come learn more about opportunities in the growing field of clinical research! 

Clinical Research Internship Program - 


Infinite Clinical Trials provide interns with real world industry experience. Interns will complete an eight-week internship twice per week for 4 hours. We pride ourselves in helping student to find careers in the field of clinical research! Instructional topics are presented in varying order depending on the flow of the trials taking place at the internship site and the time allotted for the internship.

Come learn more about opportunities in the growing field of clinical research! 

Clinical Research Internship Program - 

Infinite Clinical Trials provide interns with real world industry experience. Interns will complete an eight-week internship twice per week for 4 hours. We pride ourselves in helping student to find careers in the field of clinical research! Instructional topics are presented in varying order depending on the flow of the trials taking place at the internship site and the time allotted for the internship.

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1.1 lntroduction to Clinical Visit FIow

Interns will shadow clinical visits throughout the day over various studies. Shadowing experience may include, but is not limited to, exposure to informed consent process, observing visit procedures, charting, and data entry.

1.1 lntroduction to Clinical Visit FIow

Interns will shadow clinical visits throughout the day over various studies. Shadowing experience may include, but is not limited to, exposure to informed consent process, observing visit procedures, charting, and data entry.

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1.2 Recruiting

Interns will be provided with protocols and observe the recruitment process.

1.2 Recruiting

Interns will be provided with protocols and observe the recruitment process.

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1.3 Clinical Skills Training

Students will train with site staff and practice competency on blood pressures and vital signs.

1.3 Clinical Skills Training

Students will train with site staff and practice competency on blood pressures and vital signs.

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1.4 Medical Terminology


Interns will be provided with medical records and observe medical histories being taken.

1.4 Medical Terminology

Interns will be provided with medical records and observe medical histories being taken.

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1.5 Laboratory Skills

Interns will observe lab procedures, learn how a centrifuge works, observe sample processing and shipping lab samples

1.5 Laboratory Skills

Interns will observe lab procedures, learn how a centrifuge works, observe sample processing and shipping lab samples

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1.6 Documentation Review

Interns will review charts, letters and other important study documents utilized by clinical research staff and gain an understanding of the filing and documentation systems.

1.6 Documentation Review

Interns will review charts, letters and other important study documents utilized by clinical research staff and gain an understanding of the filing and documentation systems.

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1.7 Quality Assurance

Interns will be given subject charts to review. Interns will have the opportunity to read monitor letters and observe how visits are prepped for review. Interns will observe informed consent review on an entire trial.

1.7 Quality Assurance

Interns will be given subject charts to review. Interns will have the opportunity to read monitor letters and observe how visits are prepped for review. Interns will observe informed consent review on an entire trial.

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1.8 Clinical Trials Overview and Data Management Systems

Students will meet department staff in Business Development, Budgets and Contracts, Accounting, lT, Recruitment, Source Document Development and Regulatory review. Interns will also view data management systems and learn to enter data and answer queries.

1.8 Clinical Trials Overview and Data Management Systems

Students will meet department staff in Business Development, Budgets and Contracts, Accounting, lT, Recruitment, Source Document Development and Regulatory review. Interns will also view data management systems and learn to enter data and answer queries.

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1.9 Observation Visits

Interns will observe screening and interim visits. Interns will observe Pharma/Clinical Research Organization / Clinical Research Associate visits (PSSV, SlV, lMV, COV) if time permits.

1.9 Observation Visits

Interns will observe screening and interim visits. Interns will observe Pharma/Clinical Research Organization / Clinical Research Associate visits (PSSV, SlV, lMV, COV) if time permits.

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2.0 Presentation

Interns will be provided with a Protocol to study. Interns will create a Power Point Presentation to present to the staff, other students, and potentially an lnvestigator.

2.0 Presentation

Interns will be provided with a Protocol to study. Interns will create a Power Point Presentation to present to the staff, other students, and potentially an lnvestigator.

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TrainingLess

Training

  • Regulatory Documents and Binder Maintenance

  • Source Documents 

  • Standard Operating Procedures 

  • Adverse Events and Safety Monitoring 

  • Preparing for Audits 

  • Institutional Review Boards, Informed Consent 

  • Good Clinical Practice Testing 

  • IATA Testing 

  • Curriculum Vitae

  • Regulatory Documents and Binder Maintenance

  • Source Documents 

  • Standard Operating Procedures 

  • Adverse Events and Safety Monitoring 

  • Preparing for Audits 

  • Institutional Review Boards, Informed Consent 

  • Good Clinical Practice Testing 

  • IATA Testing 

  • Curriculum Vitae

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EligibilityLess

Eligibility

The Program is limited to U.S. citizens (or persons having U.S. Permanent Resident status)

  •  Must be at least 21 years of age.

  • Pursing a career as a Clinical Research Coordinator: 2 years of college credit, licensed vocational nurse diploma, or medical assistance license.

  • Pursuing a career as a Clinical Research Associate: an undergraduate degree at an accredited US college or university.

  • A passing drug screen and background check with no felonies.

  • Applying interns should have a strong desire to pursue a career in the field of clinical research and healthcare.

The Program is limited to U.S. citizens (or persons having U.S. Permanent Resident status)

  •  Must be at least 21 years of age.

  • Pursing a career as a Clinical Research Coordinator: 2 years of college credit, licensed vocational nurse diploma, or medical assistance license.

  • Pursuing a career as a Clinical Research Associate: an undergraduate degree at an accredited US college or university.

  • A passing drug screen and background check with no felonies.

  • Applying interns should have a strong desire to pursue a career in the field of clinical research and healthcare.

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To ApplyLess

To Apply

Fill out the form below, including your preferred timeframe to start . Once it’s been submitted you will receive a call from one of our admissions advisors, and they will help you through the rest of the application process.

Fill out the form below, including your preferred timeframe to start . Once it’s been submitted you will receive a call from one of our admissions advisors, and they will help you through the rest of the application process.

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To apply, please initiate the form

To apply, please initiate the form

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Submit