Employment Opportunities

Who We Are

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Diablo Clinical Research, Inc., a private research facility in Walnut Creek, California, is seeking highly motivated and competent individuals who enjoy contributing to high-quality research. At Diablo Clinical Research we conduct Phase 1-4 clinical studies across multiple therapeutic areas, including Diabetes, Diabetic Neuropathy, Obesity, Cholesterol, Migraines, Osteoporosis, Arthritis, Sexual Dysfunction, and more.

Our Benefits

At Diablo Clinical Research we currently offer the following benefits to our full-time employees:

  • 401(k) including employer matching contributions
  • Health Insurance
  • Dental Insurance
  • Group Life Insurance
  • Paid Vacation and Sick Time
  • Flexible Spending Plan

Diablo Clinical Research reserves the right to modify its employee benefits at any time. Diablo Clinical Research is an Equal Opportunity Employer (EOE). Qualified applicants are considered for employment without regard to age, race, color, religion, sex, national origin, sexual orientation, marital status, veteran status or disability.

Please inform us if you need assistance or an accommodation during the application process because of a disability. Diablo Clinical Research is pleased to provide such assistance, and no applicant will be penalized as a result of such a request.

Career Opportunities

Coordinator

Overview

Date Posted
4/1/13
City
Walnut Creek
Country
United States of America
Job Type
Regular

Description

We have a staff of 5 MDs (2 endocrinologists, 2 internists and 1 cardiologist, 7 coordinators, 2 regulatory personnel, 1 internal data manager/monitor, 1 lab technician, 1 registered dietician, 4 recruiters/marketing personnel and additional administrative staff to support our coordinators in the accurate and timely execution of their study protocols.

At our site, the coordinator is the primary point of contact for the study patient and sponsor representatives. The CRC works closely with the PI and Sub-Investigator to ensure the safety and well-being of the study patient is protected. We are a fast-paced office with coordinators seeing 3-5 patients per day.

Essential duties and responsibilities:

  1. Obtaining informed consent per ICH/GCP and site SOPs.
  2. Interviewing and collecting data from study participants.
  3. Scheduling subject visits.
  4. Obtaining subject vital statistics (including height, weight, BMI, pulse, respiratory rate, blood pressure, etc.) and ECGs.
  5. Dispensing/collecting study medication and providing accurate Investigational Product accountability.
  6. Collecting subject laboratory specimens according to protocol.
  7. Completing case report forms (CRFs) and other patient tracking information (either electronic or manual) accurately and on a timely basis as assigned.
  8. Maintaining a thorough understanding of all data collection instruments and collecting data accurately and according to protocol.
  9. Performing basic data manipulation.
  10. Other duties as assigned.

This position requires flexibility, excellent organizational/communication skills and attention to detail.

Minimum Requirements

  • Bachelor’s degree (BS) or RN and a minimum of 1 year experience in a clinical research setting
  • Phlebotomy certification and experience preferred;¬†Diabetes education and experience will be given priority; one of our primary study areas is diabetes and its related medical conditions (neuropathy, etc) and potential candidate would be the primary coordinator on studies for this indication
  • Preferred knowledge of the design and conduct of clinical studies
  • FT Monday – Friday with some evening and/or weekend work as needed
  • Willing to travel to off-site investigator meetings as necessary