Clinical Research Coordinator

Clinical Research Coordinator

Eastside Research Associates

Eastside Research Associates is a fast-growing medical research company that is seeking an experienced, professional Clinical Research Coordinator to execute clinical research studies according to ICH/GCP guidelines and FDA regulations. We are looking for someone who can take the initiative and coordinate multiple studies at one time. Someone who has worked in a high-paced, fast-moving environment will work well at Eastside Research Associates. Previous experience in a private research setting is a must.

Responsibilities:

• Direct oversight and management of at least 1 active research study from beginning to end
• Coordinates the operations of research studies in multiple specialties in collaboration with other research coordinators
• Provide input regarding IRB correspondence and regulatory documentation. Submit documentation as required
• Serves as the main point of contact with sponsors
• Serve as a liaison between clinical teams, patients, and sponsors
• Creates and maintains regulatory binders for each study assigned to
• Manages study data and study results
• Direct Patient care
• Review study candidates’ medical records for study eligibility
• Establishes and maintains research patient records and databases
• Oversite of the RA staff on the studies
• Consent patients for clinical research studies
• Maintain case report forms, charts, and documentation
• Ensure strict compliance with established research protocols and standards along with all applicable laws, regulations, policies, and procedural requirements
• Data collection and entry
• Manage investigational devices and drug inventory
• Take EKGs and vital signs
• Completes case report forms based on source documentation and protocol parameters
• Enters and tracks patient information and activity in research study databases
• Processes and ships research specimens per protocol
• Creates and maintains regulatory binders for each study assigned to
• Misc. duties as assigned

Qualifications:

• Clinical skills; MA or equivalent preferred
• Phlebotomy experience preferred
• Minimum 2 to 3 years of clinical research coordinator experience in a private research setting
• Excellent communication and organizational skills
• Detail-oriented
• Strong organizational and time management skills
• Familiarity with the Code of Federal Regulations as they pertain to human subject protection
• Strong computer skills

Job Type: Full-time

Salary: $30.00 - $45.00 per hour

Schedule: Monday to Friday

Work Location: Redmond, WA (on-site)

Education: AA degree or above

Benefits:

• 401(k)
• Dental Insurance
• Health Insurance
• Paid time off
• Vision Insurance
• Wireless Internet Stipend

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