Clinical Operations Study Management Intern

7 days ago


Pleasanton, California, United States Roche Full time

Job Summary

The Clinical Operations Study Management Intern will play a key role in supporting the design, planning, execution, monitoring, and closure of clinical studies within Roche Diagnostics Solutions. This internship will provide hands-on experience in clinical operations, including training on RDS policies and procedures, creating and implementing training, processes, and tools to support the Clinical Operations Study Management team.

Key Responsibilities

  • Conduct clinical trials within Invitro Diagnostics
  • Support activities related to eClinical Support Solutions tools such as CTMS and eTMF
  • Collaborate with the Clinical Operations Study Management team to ensure compliance with regulatory requirements and sponsor responsibilities
  • Develop and implement training programs to support the Clinical Operations Study Management team

Program Highlights

  • Intensive 12-week paid internship
  • Opportunity to work with a talented team in the biotechnology industry
  • Ownership of challenging and impactful business-critical projects
  • Stipend provided to help alleviate costs associated with the internship

Requirements

  • BS or MS degree in a relevant field (Biology, Medical Technology, Biochemistry, Microbiology/Immunology)
  • Course work experience in Biological Sciences
  • Understanding of the regulatory environment and requirements of the In-Vitro Diagnostics development process
  • Minimum availability of 12 weeks

Preferred Qualifications

  • Excellent communication, collaboration, and interpersonal skills
  • Complements Roche's culture and standards (Integrity, Courage, and Passion)


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