Research Coordinator 2

Job Description

Your Job: In this highly technical, fast-paced, and challenging position, you'll collaborate with multidisciplinary team members to provide the very best care for our patients. The Research Coordinator 2 performs coordination of all phases of the research process.

Responsibilities

• Attainment of the approval process required
• Coordination of data collection, management, patient follow-up and tracking
• Available to sponsor monitors upon study site visits
• Maintain statistical information
• Following all rules and regulations from the FDA, IRB, and other agencies designated by the sponsors
• Initiating and maintenance of IRB regulations (including completion of all required documents for submitting for IRB approval)
• Coinciding all phases of assigned clinical trials: Ensuring protocol compliance; Collecting, interpreting and reporting all clinical data
• Maintaining drug inventory
• Preparing charts for clinic: Pull charts prior to clinic visit
• Organization of data pertinent to clinic visit
• Completing case report forms
• Attending regular meetings with physicians and other research staff in order to get updates on the progress of the research studies/patients on treatment
• Tracking lab results and obtaining final result for NP or Physicians to review: Making sure lab results are received in a timely manner
• Triaging all phone calls for patients (research related or standard of care) considering treatment, on treatment or being followed after treatment
• Assistance with writing protocols
• Performing study related procedures (lab processing, etc)
• Follow patients throughout study
• Developing a working knowledge of disease process under study
• Performing rating scales and/or tools under investigation
• Communicate clearly and openly
• Build relationships to promote a collaborative environment
• Be accountable for your performance
• Always look for ways to improve the patient experience
• Take initiative for your professional growth
• Be engaged and eager to build a winning team

Requirements

• Bachelor degree or Medical Assistant in appropriate discipline
• RN Degree preferred
• Medical Assistant Certification, and/or a Certified Clinical Research Coordinator (CCRC) required
• LVN or RN license, preferred
• 2 or more years of related experience

Qualifications

• None specified

Skills

• Excellent communication skills
• Strong organizational skills
• Attention to detail
• Ability to work independently and as part of a team
• Knowledge of regulatory requirements
• Proficiency in Microsoft Office Suite

Benefits

• Comprehensive health insurance
• Retirement plan
• Flexible work schedule
• Professional development opportunities
• Employee assistance program

Pay

• Competitive salary based on experience and qualifications

Schedule

• 40 hours per week
• Monday through Friday