Clinical Trial Manager - Irvine, United States - Provident Research Inc

Provident Research Inc
Provident Research Inc
Verified Company
Irvine, United States

2 weeks ago

Mark Lane

Posted by:

Mark Lane

beBee recruiter
Description

Clinical Trial Manager - Major Medical Device CorpWe'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 onsite 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, $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 required)

Work Location:
In person
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