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Clinical Operations Intern

Apply Share Job ID 816 Category Internship Job Location Redwood City, California Posted Date 04/21/2018

Overview:

POSITION OVERVIEW

The Clinical Operations intern will work closely with Clinical Operations staff to support the management of clinical studies for the development and commercialization of novel assays which lead to improved treatment decisions for oncology patients. This position will also support department projects and initiatives, as assigned.

The ideal candidate will be detail oriented, a self-starter, a strategic thinker, and interested in clinical trial management. Some knowledge of Good Clinical Practice (GCP) and ICH guidelines is a plus.

The Intern will report to a Senior Clinical Trial Manager within the Clinical Operations organization.

RESPONSIBILITIES / DUTIES

- Study file maintenance (electronic and/or hard copy);
- Document tracking and signature/approval follow-up (including Confidential Disclosure Agreements (CDAs), contracts, protocols, and other documents required in the study file);
- Creating and maintaining study/project contact lists and tracking tools for budget, enrollment, samples, site supplies, and other study-specific needs;
- Meeting scheduling and logistics (including food & beverage coordination, call/web conference activation, resolution of technical issues, distribution of agendas and generation of meeting minutes);
- Maintaining study timelines;
- Microsoft Office support for study and department documents;
- Other tasks/project support as assigned;
- Perform all responsibilities in accordance with applicable Standard Operating Procedures, guidelines and work instructions

QUALIFICATIONS

REQUIRED:
- Pursuing a BS in an applicable field with a specific interest in health care, genomics, clinical trial management and/or diagnostics.
- Demonstrated competence with Microsoft Office (Word, Excel, and PowerPoint)
- Well organized and detail-oriented;
- Comfortable in a fast-paced, rapid growth environment.
- Strong oral and written communicator with ability to maintain open communication with internal employees, managers and customers as needed
- Able to prioritize and drive to results with a high emphasis on quality
- Able to work as part of a team
- Able to integrate and apply feedback in a professional manner

PREFERRED:
- Knowledge of Good Clinical Practice (GCP) and ICH guidelines
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If you want to be part of a team that prides itself in teamwork and developing cutting-edge technology at Genomic Health, apply today!