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.
Current Job Openings:
Coordinator
Diablo Clinical Research is a dedicated research facility that conducts Phase I-IV pharmaceutical studies across multiple therapeutic areas (diabetes, obesity/weight loss, cholesterol, hypertension, fibromyalgia, osteoporosis, osteoarthritis, neuropathy, migraines and more).
We have a staff of 6 MDs (2 endocrinologists, 2 internists, 1 cardiologist and 1 neurologist), 8 coordinators, 2 regulatory personnel, 1 internal data manager/monitor, 1 lab technician, 1 RD/CDE, 6 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.
This position requires flexibility, excellent organizational/communication skills and attention to detail.
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.
POSITION REQUIREMENTS:
Education: 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.
FT Monday - Friday with some evening and/or weekend work as needed.
Willing to travel to off-site investigator meetings as necessary.
Knowledge: Preferred knowledge of the design and conduct of clinical studies.
Please visit our website at www.diabloclinical.com to learn more about our growing company.
Interested applicants should submit a cover letter (referencing the applicable JobID) and a resume or Curriculum Vitae via e-mail to lvitti@diabloclinical.com. Please do not contact Diablo Clinical Resesarch by telephone or by facsimile. If you are selected to interview for a position with Diablo Clinical Research, our Human Resources Department will contact you.
At Diablo Clinical Research we currently offer the following benefits to our employees:
- 401(k) including employer matching contributions
- Health Insurance - 100% paid for the employee
- Dental Insurance
- Group Long Term Disability 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.
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