CDMA Clinical Operations Study Management Intern

Found in: Talent US C2 - 1 week ago

Pleasanton, United States Roche Full time

The Position

Department Summary

Roche Diagnostics Solutions innovates diagnostics, shape healthcare and change lives by ensuring that all studies are designed, planned, executed, monitored, closed out and documented in an appropriate manner within the planned timeframe and cost, securing that the sponsor responsibilities are fulfilled, while assuring compliance to all applicable regulatory requirements and providing oversight to outside support including CROs, consultants and/or medical advisors.

This internship position isFully remote.

Key Responsibilities

The candidate will conduct clinical trials within Invitro Diagnostics. Training on RDS policies and procedures involved in, and related to, Clinical Operations both in pre-launch and post-launch studies. Creating and implementing training, process and tools to support the Clinical Operations Study Management team

Support activities related to eClinical Support Solutions tools such as CTMS and eTMF

Program Highlights

Intensive 12-weeks paid internship.

Program start dates May/June (Summer 2024)

A stipend, based on location, will be provided to help alleviate costs associated with the internship. 

Ownership of challenging and impactful business-critical projects.

Work with some of the most talented people in the biotechnology industry.

Previous experience in the job duties listed, either through course work or industry/academia

Participation in student organizations and/or other leadership experience

Who You Are

Required Education

Just BS & MS: Undergraduates who have completed at least 3 years of undergraduate coursework at a university, or current graduate students pursuing a Masters or recent grads (BS or MS) within two years.

Preferred Majors: Biology, Medical Technology, Biochemistry, Microbiology/Immunology

​

Required skills: 

●Course work experience in Biological Sciences

●Understanding the regulatory environment and requirements of the In-Vitro Diagnostics development process.

●Completed at least 3 years of college/university to be eligible for the program.

●Must have a GPA

●Minimum availability of 12 weeks (Required start on or before program Welcome Reception and end date on or after Summer End Poster Symposium).

Other Preferred Qualifications

Excellent communication, collaboration, and interpersonal skills.

Complements our culture and the standards that guide our daily behavior & decisions: Integrity, Courage, and Passion.

The expected salary range for this position based on the primary location for this position in California is - per hour. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position also qualifies for paid holiday time off benefits

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