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Intern Start Work Tomorrow Jobs in Ohio (NOW HIRING)

This group plays a key role in the study start-up/site activation process at Medpace by ... Availability to work full-time (40 hours/week) in our Cincinnati, OH office. Travel: None Medpace ...

This group plays a key role in the study start-up/site activation process at Medpace by ... Availability to work full-time (40 hours/week) in our Cincinnati, OH office. Travel: None Medpace ...

Purchasing Intern

Columbus, OH · On-site

$17.50 - $23.50/hr

If you're willing to contribute and create value for tomorrow's cleaner and smarter mobility ... High performers. Globally minded people who aspire to work in a transforming industry, where ...

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Intern Start Work Tomorrow information

What is an intern start work tomorrow?

An 'Intern Start Work Tomorrow' position refers to an internship opportunity where the selected candidate is expected to begin working as soon as the next day. This typically indicates an urgent hiring need, and the responsibilities can vary depending on the industry and employer. Interns may assist with administrative tasks, support ongoing projects, or gain hands-on experience in their field of study. It’s important to be ready to adapt quickly and learn on the job. Applicants should be prepared to start immediately and demonstrate flexibility and eagerness to contribute from day one.

What can I expect during my first week as an intern starting immediately?

During your first week as an intern, you can expect a combination of orientation activities, training sessions, and introductory meetings with your team. You'll likely spend time learning about company policies, familiarizing yourself with workplace tools, and understanding your primary responsibilities. It's common to shadow team members and participate in small assignments to get hands-on experience. Don't hesitate to ask questions—your supervisors and colleagues expect you to be new and are there to help you succeed. Building relationships early on will set a positive tone for your internship.

What are the key skills and qualifications needed to thrive as an intern, and why are they important?

To thrive as an Intern, you generally need a foundational knowledge in your field of study, relevant coursework or training, and a willingness to learn. Familiarity with standard productivity tools like Microsoft Office or Google Workspace, and sometimes basic knowledge of industry-specific software, is often expected. Strong communication, adaptability, and a proactive attitude help interns stand out and build positive relationships within the team. These skills and qualities are important for making a strong impression, contributing effectively, and maximizing learning opportunities during the internship.

What is the difference between Intern Start Work Tomorrow vs Intern Assistant?

AspectIntern Start Work TomorrowIntern Assistant
Required CredentialsHigh school diploma or ongoing college courseworkHigh school diploma or college coursework, sometimes with specific skills
Work EnvironmentEntry-level, supervised, temporaryEntry-level, supervised, temporary
Industry UsageCommon in various industries for initial trainingCommon in administrative, healthcare, and technical fields
Search & Comparison IntentUnderstanding start date and role expectationsClarifying responsibilities and role differences

Intern Start Work Tomorrow typically refers to an internship beginning the next day, focusing on initial training and observation. Intern Assistant often indicates a supportive role assisting with tasks, sometimes with specific skills. Both are entry-level, temporary positions, but the main difference lies in the role's focus and responsibilities.

Study Start-Up Intern

Medpace, Inc.

Cincinnati, OH • On-site

Other

Medical, Retirement, PTO

Posted 19 days ago


Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

16th of 75 rated research


Job description

Job Summary
Our clinical operations activities are growing rapidly, and we are seeking a full-time, office-based intern to support our Regulatory Submissions team within our Site Activation and Maintenance (SAM) Department for fall 2026. This group plays a key role in the study start-up/site activation process at Medpace by communicating with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in a clinical trial. The Regulatory Submissions Intern will provide support to the Regulatory Submissions Coordinators and Managers as they maintain start-up timelines, review and collect regulatory documents, and proactively identify solutions to regulatory issues.
Responsibilities
  • Provide support to the study start-up team through completion of compliance tasks
  • Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF);
  • Gain hands-on training and exposure to the clinical trial start-up phase through our Site Activation & Maintenance (SAM) Training Program as outlined below.

SITE ACTIVATION & MAINTENANCE (SAM) TRAINING PROGRAM
  • Medpace training programs are curated to educate and support experienced associates, as well as those that are new to the industry. The SAM Training Program embraces evidence based learning & development models to advance professional learning and employee performance. In the program, you will...
  • Complete independent learning modules, interactive exercises, and team workshops through the core curriculum;
  • Gain exposure to real-world tasks through a robust mentoring program; and
  • Join other professionals revolutionizing efficient and seamless study start-up to advance clinical trials.

Qualifications
  • High School Diploma, pursuing Bachelors degree in life science field
  • Graduating in December 2026 or May 2027
  • Excellent organizational and prioritization skills
  • Knowledge of Microsoft Office
  • Availability to work full-time (40 hours/week) in our Cincinnati, OH office.

Travel: None
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture
    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development
    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits
    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience
    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

What Medpace employees say

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Benefits

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992