Clinical Trial Manager

1 month ago


Irvine, United States Provident Research Inc Full time

**Clinical Trial Manager - Major Medical Device Corp**We're seeking an experienced Clinical Trial Manager or equivalent with at least 6 years of clinical trial management experience for this terrific role within a major Medical Devices Company. This is a Hybrid role that is divided into work-from-home and work from corp. offices in Irvine, CA.

This is a full-time salaried (W2) position with excellent compensation and benefits. As a Clinical Trial Manager, you will be working with clinical development colleagues focused on Ophthalmic medical devices.

Applicants **must have** medical or technical experience managing clinical research for either/or Ophthalmic **Medical Devices** or **Drugs.** You must have experience managing clinical trials working with Ophthalmologists, Optometrists, and other healthcare providers who treat illnesses or diseases of the eye.
- The CTM will be responsible for all aspects of project management from study planning and startup through completion and database lock.
- CPM is responsible for managing clinical projects while supporting regulatory affairs, data management, medical writing, biostatistics, and on-site monitoring functions.
- Experience with clinical study budgets and vendor selection & management is required.
- U.S. clinical project management experience is required, and familiarity with international studies is a plus.

Pay: $135,000.00 - $145,000.00 per year

**Benefits**:

- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance

**Experience**:

- Clinical trials management: 5 years (required)
- Ophthalmology: 2 years (required)

Ability to Commute:

- Irvine, CA 92618 (required)

Work Location: In person



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