The International Clinical Trials Registry Platform (ICTRP) has a strong internship program which welcomes interested and enthusiastic students, professionals, and researchers from a wide range of disciplines. The internship with the ICTRP is flexible and tailored to individual learning goals to provide interns with the best possible experience with the ICTRP at the World Health Organization.
Internships with the ICTRP provide an excellent opportunity to participate in the work of health policy related to clinical trials, research transparency, and knowledge sharing.
Yale University – New Haven, CT
An internship that provides an opportunity to develop professional skills in a wide variety of fields and to support various University initiatives. Observes and gains expertise in applicable areas. Assists and completes various projects, programs, and assignments.
1. Supports and coordinates a range of academic programs.
2. Works on various programs throughout the year; including researching and writing of highly confidential material and working with other departments within the University.
3. Interacts with faculty, students and staff within and outside of the University.
Varian Medical Systems – Seattle, WA
They are in charge of generating clinical evidence to support business needs. As an intern on our team, you will have the opportunity to immerse yourself in clinical evidence gathering and analysis of clinical evidence relating to oncology treatments and associated medical devices. Gathering clinical evidence is an important activity to bringing a medical device to market and is essential in meeting requirements for keeping a released medical device on the market, and it might be obtained through clinical studies, registry studies, and published literature. This aspect of medical device development is often not made apparent to students, so it would allow the intern to gain wider exposure to clinical evidence gathering and related analysis methods that they would normally not have from an academic field. The intern is also responsible for developing electronic data collection forms for gathering data from clinical/registry studies, analyzing the data, and generating reports.
Pharmaceutical Product Development – Wilmington, NC
Between a pharmaceutical and biotechnological innovation and a drug delivered, between an idea for a cure and a population that needs it.
Thousands of employees in locations worldwide connected by tenacity and passion for our purpose which is to improve health.
Their Clinical Internship program helps you start your career in the field and to also apply your industry knowledge to real-life challenges. As an intern, you will be exposed to a range of areas within PPD but spend the majority of your time dedicated to one department. You'll also have the opportunity to experience different pieces of training and shadow professionals in a variety of roles.
CRA job opportunities
As a Clinical Research Associate (CRA), you will have a key role in the success of clinical trials. You will be the primary contact and support for trial sites, ensuring that the study is conducted according to the protocol, ICH-GCP, regulatory requirements and standard operating procedures (SOPs).
The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them.
Take courses from CCRPS and learn more on how to become a clinical research associate.
Discover more from Clinical Research Training | Certified Clinical Research Professionals Course