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Clinical Research Coordinator
Palm Springs, California Desert Regional Medical CenterEmbark on a rewarding career with Desert Regional Medical Center hospital. If you are a compassionate healthcare professional eager to contribute to patient care, this is your opportunity where your skills make a difference every day. Join us in delivering exceptional healthcare with a personal touch.
At Desert Regional Medical Center, we understand that our greatest asset is our dedicated team of professionals. That’s why we offer more than a job – we provide a comprehensive benefit package that prioritizes your health, professional development, and work-life balance. The available plans and programs include:
- Medical, dental, vision, and life insurance
- 401(k) retirement savings plan with employer match
- Generous paid time off
- Career development and continuing education opportunities
- Health savings accounts, healthcare & dependent flexible spending accounts
- Employee Assistance program, Employee discount program
- Voluntary benefits include pet insurance, legal insurance, accident and critical illness insurance, long term care, elder & childcare, auto & home insurance
Note: Eligibility for benefits may vary by location and is determined by employment status
A Clinical Research Coordinator is responsible for a variety of duties including the following:
• Overseeing the trouble-free running of clinical trials
• Collecting data obtained from research, coding and analyzing it
• Managing budgets set aside for research
• Communicating with participants regarding study objectives
• Administering questionnaires and monitoring participants to ensure they adhere to the study’s rules
• Liaising with laboratories regarding research findings
• Monitoring the study to ensure that it complies with protocols, is ethically-conducted and follows regulatory standards
• Maintaining research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelines
• Directing the collection, labeling, storage and transport of all specimens
• Making sure that all equipment and supplies needed for the study are in-stock and in good working order
Shift: Day
Job type: Full Time
Hours:
POSITION SUMMARY:
A competent Clinical Research Coordinator should be able to perform various duties and responsibilities. Proper fulfillment of a Clinical Research Associate’s duties and responsibilities brings success to your company. Clinical Research Associates should assist in organizing and monitoring the different stages of clinical trials. The following are other duties and responsibilities a should be able to execute:
• Supervise study sites and activities to ensure adherence to appropriate industry protocols and terms of the study
• Collect and authenticate data collection forms otherwise known as case report forms
• Screen potential study participants through medical record reviews, interviews and follow-ups with healthcare providers
• Coordinate with ethics committees to safeguard the rights, safety and wellbeing of all research subjects and research activities
• Maintain specific records of research activity to include regulatory forms, drug dispensation records, case reports and consent forms
• Prepare final reports, occasional manuscripts or publication, New Drug Applications (NDAs) and Biological License Applications (BLAs)
• Ensure proper transmission of clinical case data to the data management centers, review case reports questions and problems and clarify or obtain alterations to data as appropriate
• Oversee research, technical and administrative staff, to include training, hiring, goal setting and distribution of workload
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