Most applicants have degrees and certificates, but few have structured CRO internship experience, giving you experience comparable to a year of early industry exposure and stronger positioning with hiring managers.
This fully remote placement is structured and guided, designed to fit alongside work or school, and built within a 4 week pathway so you gain internship level exposure without pausing your life.
This placement with CRO partners follows a structured internship framework with guided clinical research tasks, creating a career focused pathway built for aspiring professionals.
Successful interns receive an official recommendation letter recognizing their performance and completion of their clinical research internship placement with our CRO partners.
Join our accelerated 4 week program and gain one year equivalent CRO industry experience. Completion is fully remote with flexible scheduling, so you can advance your clinical research career without taking time off work or school.
Gain structured experience in trial operations support, documentation workflows, study coordination processes, and CRO communication systems.
Develop exposure to monitoring principles, source documentation review, protocol compliance, and site-level regulatory processes aligned with CRA responsibilities.
Build foundational exposure to safety reporting concepts, adverse event documentation principles, regulatory standards, and clinical data review processes.
Select a structured internship track aligned with your intended clinical research role and build targeted experience designed to support your long term professional direction.
This pathway builds a strong operational foundation for individuals seeking flexibility across roles such as Clinical Trial Assistant, Clinical Research Coordinator, TMF Manager, Study Support roles, and future CRA pathways. It is ideal for those who want to strengthen core competencies and keep multiple career options open. Apply Now
Develop strong foundational exposure to monitoring principles, source documentation review, protocol compliance concepts, investigational product accountability, and site-level regulatory processes aligned with Clinical Research Associate responsibilities.
This track is intentionally designed to build core competencies that are essential not only for the CRA pathway, but also foundational for entry into multiple clinical research roles, including Clinical Research Coordinator, Clinical Trial Assistant, and other site and sponsor-facing positions. Apply Now
Build foundational exposure to safety reporting concepts, adverse event documentation principles, regulatory safety standards, and clinical data review processes. This track is structured for those interested in drug safety and pharmacovigilance careers. Apply Now
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“Excellent training, valuable internships, and strong career support. Obedtek stands out as a unique pathway with strong impact for anyone serious about breaking into clinical research.”
"Internships help you get in the door, learn on the job, and can lead to full-time roles."
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