Job Description

Requisition Number 07381
Department Name: G&A - Li
Position Type: Full Time
Position Title Medical Monitor
Position Summary:

The Medical Monitor will be responsible for providing safety oversight and reviewing the protocol and information about the study investigation product as it becomes available, such as the Investigational Brochure (IB), and reported safety events including SAE narratives, SUSARs and communicating with sites if new information emerges. In consultation with the CMO, the protocol team and clinical review committees (or Data Safety Monitoring Boards), will provide safety review during the execution of the clinical trial.

Position Description

* Provides medical oversight for clinical trials including reviewing safety information and providing applicable recommendations.
* Recommends, as appropriate, medical management to site investigators
* Updates members of the study team regarding safety information
* Facilitates early detection of safety signals and maximizes the chances for continued appropriateness of the research and protection of human subjects.
* Undertakes activities as may be requested by the CMO time to time

Location: San Diego, California
Additional Information:
Physical Requirements:

This position works in a typical office environment. With or without reasonable accommodation, employees in this position must be able to sit and type at a computer terminal for up to 8 hours per day with appropriate breaks and perform tasks that require fine dexterity and repetitive motions using the arms, hands, wrists and fingers. Further details of the physical requirements of established essential functions for this position will be addressed/discussed during the interview process. Frequent travel to clinical sites required.

Basic Qualifications:

* MD Required
* Specialization in Oncology or related field
* 5-10 years direct experience in the pharmaceutical industry, preferably in a
medical monitoring role.
* Understanding of drug safety regulations and processes and clinical trial oversight
* Experience providing input into key regulatory documentation.
* Excellent interpersonal and communication skills with ability to relate to both internal and external stakeholders.
* Strong communication and presentation skills as well as an ability to communicate clearly and concisely in writing.
* Experience presenting to a wide variety of audiences including internal teams and medical/scientific communities

Preferred Qualifications:
Compensation: DOE
Job Closing Date:
Open Until Filled Yes
Job Posting Category Scientific & Technical
EEO Statement

The Scripps Research Institute is an Equal Opportunity Employer. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other legally protected characteristic or status.

Application Instructions

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