Clinical Research Assistant

We are looking for a Clinical Research Assistant to support the Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols while providing an impeccable patient experience in every single interaction.

Requirements

• Works directly with the site operations team to coordinate the trial process.
• Assists in educating patients about the nature of their disease and the benefits and risks of participating in a clinical drug trial.
• Determines protocol-related needs to conduct the trial and order supplies and equipment.
• Recruits and screens potential patients and obtains informed consent.
• Assists in providing patient education on the benefits and risks of participating in a clinical drug trial.
• Completes source documents and forms to facilitate accurate data collection and record keeping.
• Conducts in-service programs and summarizes study schedules to assist in understanding and implementing a protocol.
• Schedules patient visits and laboratory and diagnostic test procedures.
• Assists with investigational product shipments, storage, and accountability.
• Reviews trends, problems encountered, patient adverse events, and patient progress.
• Performs other clinical skills as required by the trial protocol, including vital signs, ECGs and blood glucose testing.

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
• 15 days of PTO + 8 paid holidays and 2 floating holidays