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The Study Pro Jobs (NOW HIRING)

Pro Bono - ABA UNPAID Intern

Chicago, IL · On-site

$15.50 - $20.50/hr

The intern will be responsible for conducting research on pro bono services and programs ... Please specify any relevant program or area of study directly related to the purpose of the ...

The study will also evaluate the impact of banning menthol cigarettes. The Research Assistant will contribute to data collection in the UNC Mini Mart. The Mini Mart is a physical convenience store ...

The study PI is an assistant professor in the college of nursing. Other co-Is are from Emory ... Robust experience with Tobii Pro Lab, particularly exporting data to be analyzed. * Must be ...

Pro-actively communicate with the Project team and vendors in order to meet sponsor requirements * Work with the study teams, advising and informing on the processes that have to be completed to ...

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How much do the study pro jobs pay per hour?

As of Jun 7, 2026, the average hourly pay for the study pro in the United States is $22.63, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $25.00 per hour, depending on experience, location, and employer.

How does a Study Pro typically collaborate with students, parents, and educators to support academic success?

A Study Pro works closely with students to develop effective study habits, time management skills, and personalized learning strategies. They regularly communicate with parents to provide updates on progress and suggest ways to reinforce positive habits at home. Additionally, they may collaborate with teachers or school counselors to align their support with classroom expectations and address specific academic challenges. This collaborative approach helps ensure that each student receives comprehensive support tailored to their unique needs.

What is the difference between The Study Pro vs Academic Tutor?

AspectThe Study ProAcademic Tutor
CredentialsVaries; often requires subject expertise or certificationsTypically requires a degree or ongoing education in the subject
Work EnvironmentOnline or in-person sessions, flexible hoursIn-person or online, often one-on-one sessions
Industry UsageEducational support, test prep, skill developmentAcademic assistance, homework help, exam prep

The Study Pro and Academic Tutor both provide educational support, but The Study Pro often offers more flexible, broader services including test prep and skill development, while Academic Tutors focus primarily on subject-specific assistance. Both roles require relevant knowledge and certifications, with work environments ranging from online to in-person sessions.

What are the key skills and qualifications needed to thrive as a Learning Coach at The Study Pro, and why are they important?

To thrive as a Learning Coach at The Study Pro, you need a background in education or child development, strong organizational skills, and experience supporting students' academic growth. Familiarity with digital learning platforms, progress tracking tools, and educational software is often required. Exceptional communication, patience, and the ability to motivate and engage students are critical soft skills in this role. These skills ensure effective personalized support, foster student independence, and help learners achieve academic success in a structured environment.

What is a Study Pro and what do they do?

A Study Pro is an educational coach or tutor who specializes in helping students develop effective study habits, executive function skills, and academic strategies. They work with students to improve organization, time management, goal setting, and test preparation. Study Pros may also support students with learning challenges by providing personalized guidance and accountability. Their goal is to empower students to become independent, confident learners.
More about The Study Pro jobs
What states have the most The Study Pro jobs? States with the most job openings for The Study Pro jobs include:
Infographic showing various The Study Pro job openings in the United States as of May 2026, with employment types broken down into 6% Locum Tenens, 16% Full Time, 5% Part Time, 5% Temporary, 65% Contract, and 3% Nights. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution, with an average salary of $47,067 per year, or $22.6 per hour.
(Associate) Medical Director - Neurology

(Associate) Medical Director - Neurology

Thermo Fisher Scientific

Cornelius, NC

Full-time

Posted 5 days ago


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 396 frontline employees who took The Breakroom Quiz

186th of 516 rated manufacturers


Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Discover Impactful Work:

The (Associate) Medical Director will provide medical support and medical advice for clinical trials and safety evaluation within the Pharmacovigilance department.

A day in the Life:

  • Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, involved in review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials
  • Real time Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well study subject safety, while ensuring medical issues are identified early. Pro-active customer concern and correction of issues in consultation with the Global Medical Indication Lead
  • During initial review of protocol, consults with internal groups and support staff regarding procedural and budgetary items and the necessity for change due to any subsequent protocol amendments. Acquires other functions’ dedication to close gaps and address issues timely and effectively. Serves as chief liaison between sponsor and all PPD, part of Thermo Fisher Scientific internal departments performing the required tasks during all study phases. Educates Investigator sites by delivering a protocol specific lab procedures presentation and demonstration during an investigator meeting. Controls, handles and follows day to day activities during the course of the clinical trial to resolve any issues and answer queries
  • Medical point of contact for all internal and external stakeholders: Interact with the investigators as needed, answer questions of IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; medical training of site staff at Investigator meetings; CRA training in new indications
  • Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP
  • Closely collaborate with the cross functional study team members in order for medical risks, issues, and results to be clear to all involved parties

Education

  • MD, MB/BS or equivalent degree and strong medical knowledge, shown clinical experience running Neurology patients in hospital practice.
  • Epileptology experience would be an advantage

Knowledge, Skills, Abilities

  • Significant experience within pharmaceutical industry, clinical trials and pharmaceutical medicine is critically important
  • Is fluent in spoken and written English
  • Shown understanding and experience with NDA submission process.
  • Shown understanding of regulatory guidelines for adverse event reporting
  • Strong communication & presentation skills and is a strong teammate

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Apply today! http://jobs.thermofisher.com

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.


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