Job Description

Clinical Research Coordinator

Must Haves: 1+ years of experience in clinical research, experience working in a fast paced setting

Hours: 40 hours per week, Monday-Friday onsite, normal business hours with some flexibility

Contract Duration: Direct Hire - permanent employee from day one

Benefits: Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 8 paid holidays and 2 floating holidays.

About the Role

RESPONSIBILITIES

• Obtaining informed consent per ICH/GCP and site SOPs.
• Reviewing and revising source documents and interviewing and collecting data from study participants.
• Participating in protocol training meetings and completing online training for protocol-specific software programs.
• Dispensing/collecting study medication and providing accurate Investigational Product accountability.
• Working with our lab specialist to obtain study participant laboratory specimens according to protocol (phlebotomy license and lab experience a plus, but not essential as we have a FT lab specialist on staff).
• Completing study participant tracking information (either electronic or manual) accurately and on a timely basis. Responding and resolving data queries in a prompt manner.
• Maintaining a thorough understanding of all data collection instruments and collecting data accurately and according to protocol.
• Performing basic data manipulation.
• Maintaining a thorough understanding of all assigned clinical trial protocols.
• Other duties as assigned.

QUALIFICATIONS

• Work experience as a CRC, preferably with a research site
• Bachelor's degree preferred.
• Phlebotomy and EKG experience preferred.
• Familiar with e-source reporting via an electronic platform
• A clear understanding of ICH, FDA, and GCP regulations
• Impeccable organizational skills and attention to detail
• Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources
• An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven
• High-level critical thinking skills
• Working knowledge of medical terminology and lab collection/processing/storage procedures
• Proficiency with computers and Microsoft Office Suite

Apply Today!

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