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Clinical Development Intern Jobs in Wisconsin (NOW HIRING)

IMAGING INTERN - CT SCAN

Wausau, WI · On-site

$16 - $21.50/hr

Clinical experiences occur under the general supervision of a registered technologist until competencies for their modality are met. The Imaging Intern is a member of the patient care team and is ...

New

IMAGING INTERN - CT SCAN

Wausau, WI · On-site

$16 - $21.50/hr

Clinical experiences occur under the general supervision of a registered technologist until competencies for their modality are met. The Imaging Intern is a member of the patient care team and is ...

New

Performs work assignments linked to clinical department projects/goals. * Performs functions within scope of authority as defined by the manager. * Organizes and prioritizes work assignments, raising ...

Clinical Intern Sleep Lab

Appleton, WI · On-site

$14.75 - $19.50/hr

Performs work assignments linked to clinical department projects/goals. * Performs functions within scope of authority as defined by the manager. * Organizes and prioritizes work assignments, raising ...

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Showing results 1-20

Clinical Development Intern information

What is the difference between Clinical Development Intern vs Clinical Research Associate?

AspectClinical Development InternClinical Research Associate
Required CredentialsTypically pursuing or recent graduate in life sciences or related fieldBachelor's degree in life sciences; often requires certification or experience
Work EnvironmentSupportive, learning-focused, often in pharmaceutical or biotech companiesField and office-based, monitoring clinical trials at sites
Employer & Industry UsageInternship programs in pharma, biotech, or medical device companiesFull-time role in clinical trial management companies or sponsors

The Clinical Development Intern role is an entry-level position focused on supporting clinical trial processes and gaining industry experience. In contrast, a Clinical Research Associate is a more experienced role responsible for monitoring clinical trials, ensuring compliance, and managing trial sites. While both roles are integral to clinical research, the intern position is more educational and supportive, whereas the CRA role involves active trial oversight and requires more experience.

What does a Clinical Development Intern do?

A Clinical Development Intern assists with various phases of clinical research and drug development under the supervision of experienced professionals. Their responsibilities may include supporting the design and implementation of clinical trials, organizing data, preparing study documentation, and ensuring compliance with regulatory guidelines. Interns often collaborate with cross-functional teams, gaining exposure to the processes involved in bringing new medical treatments to market. This internship is an excellent opportunity for students or recent graduates interested in clinical research or pharmaceutical development.

What are the key skills and qualifications needed to thrive as a Clinical Development Intern, and why are they important?

To thrive as a Clinical Development Intern, you need a background in life sciences or a related field, with strong analytical and research skills. Familiarity with clinical trial protocols, regulatory guidelines (like GCP), and data management systems is typically expected. Attention to detail, effective communication, and a collaborative mindset are essential soft skills for this role. These skills are important to ensure high-quality clinical research, regulatory compliance, and smooth teamwork in fast-paced clinical environments.

What types of projects or tasks can a Clinical Development Intern expect to work on during their internship?

As a Clinical Development Intern, you can expect to participate in a variety of projects that support the design and execution of clinical trials. Typical tasks may include assisting with protocol development, data collection, and documentation, as well as helping coordinate communication between clinical sites and internal teams. You may also be involved in reviewing regulatory documents and supporting the preparation of study reports. This role often requires strong attention to detail and the ability to collaborate with cross-functional teams, providing valuable exposure to the clinical research process.
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What job categories do people searching Clinical Development Intern jobs in Wisconsin look for? The top searched job categories for Clinical Development Intern jobs in Wisconsin are:
What cities in Wisconsin are hiring for Clinical Development Intern jobs? Cities in Wisconsin with the most Clinical Development Intern job openings:
Maydm Intern - Process Development

Maydm Intern - Process Development

Catalent Pharma Solutions

Madison, WI • On-site

$15 - $20.25/hr

Full-time

Posted 9 days ago


Catalent rating

7.4

Company rating: 7.4 out of 10

Based on 52 frontline employees who took The Breakroom Quiz

53rd of 73 rated pharmaceutical


Job description

Internship: Process Development

Position Summary:

  • Work Schedule: Monday - Friday
  • 100% on-site
  • Internship

Catalyst + Talent

A Catalent internship offers you countless opportunities to have direct impact on the health and well-being of millions of people globally! Your passion for learning coupled with Catalent's superior technologies will help drive the advancement of medicine in collaboration with leading pharmaceutical, biotech and health care innovators.

The Catalent Internship Experience includes:

  • Opportunity to make an impact in the lives of patients all over the world!
  • Experience through hands-on projects that support more superior drug development and delivery technologies than anyone else.
  • Exposure to top-tier scientistsand industry leaders.
  • Commitment from dedicated managers and mentors who are advocates for your success and career development.
  • Access to collaborative and highly engaged colleagues across the globe excited to share their knowledge and provide you support.

The Process/Product Development team supports the development and delivery of scalable, cost-effective processes for cell and gene therapies from pre-clinical through Phase III production. In this internship, you will assist with non-GMP lab activities across Process Development and Manufacturing, gaining hands-on experience with equipment, documentation standards (GLP vs. GMP), and process mapping. The Process Development Intern also includes maintaining lab organization, supporting purification operations, preparing reagents, documenting work per SOPs, and contributing to team operations and continuous improvement efforts.

The Role:

  • Maintain organization and uphold 5S standards in development and pilot labs
  • Conduct and document 5S audits, implementing updates as needed
  • Support large-scale purification operations and lab activities
  • Perform data entry and ensure accurate recordkeeping
  • Maintain batch production records and complete documentation in compliance with SOPs
  • Execute routine and preventative maintenance on laboratory equipment
  • Prepare buffers and contribute to writing equipment and media SOPs
  • Provide general lab support, including cleaning, and actively participate in team meetings
  • Other duties as assigned

The Candidate:

  • Eligible to legally work in the United States
  • Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds

Why you should join Catalent:

  • Potential for career growth on an expanding team
  • Abundance of cross-functional exposure to other areas within the organization

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.


What Catalent employees say

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Benefits

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About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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