Job Summary:
A clinical research coordinator is a key figure in clinical research projects, responsible for
overseeing and managing various aspects of clinical trials and studies. Their primary role is to
ensure that research protocols are implemented efficiently, ethically, and in compliance with
regulatory requirements.

Duties/Responsibilities:
• Coordinate participant study visits
• Prepare charts and supplies for study visits
• Lead participant tests, procedures, and eDiary set up
• Data entry for study visits
• Maintain participant charts
• Send participant reminders for eDiary completion, fasting visits, etc.
• Attend SIV/IM for primary studies
• Study monitor interactions for site specific and/or patient issues
• Assist study monitors during scheduled IMV/COV
• Remote monitor interactions when needed
• Manage investigational product supplies for primary studies
• Dispense investigation product or study medication to participants
• Answer queries for primary studies as needed
• Complete necessary trainings
• Keep ISF logs updated for primary studies
• Point of contact for patient related escalations/issues (e.g. AE, SAE, compliance issues,
eligibility concerns, unblinding)
• Review medical records with investigator when received to ensure all study criteria are
met
• Attend and contribute to weekly CRC meetings
• Attend and contribute to quarterly staff meetings
• Daily emails (~25-50 emails)
Skills/Abilities:
• Previous laboratory or clinical research experience preferred
• Excellent organizational skills and ability to work in a fast-paced environment
• Calm under pressure and capable of solving sudden problems that may not have clear
answers or readily available resources
• Proficient in navigating unfamiliar technology and programs independently and adeptly
such as site CTMS
• Personable
• Effective communicator who can cooperate as a member of a team
• Ability to prioritize, multitask and work independently within a hierarchy
• Proficient with Microsoft Office 365 suite

Education and Experience:
• Bachelor’s degree or higher or equivalent clinical research experience preferred

Physical Requirements:
• Means and ability to commute to both offices in Media, PA and West Chester, PA
• Prolonged periods of sitting at a desk and working on a computer
• Must be able to lift up to 30 pounds

Wage/Salary: Starting at $22/hour