Clinical Research Assistant

SQRL; Walnut Creek (CA); On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

401k with match

15 days PTO

Great opportunity in clinical research

Job summary

SQRL is seeking a dedicated individual for a clinical research role based in Walnut Creek, California. The role involves coordinating research trials, educating patients on trial specifics, and recruiting study participants while ensuring protocol adherence.

The ideal candidate will have at least 1 year of experience in a medical setting, preferably with a Bachelor's degree. Experience in phlebotomy and EKG is a plus. This position offers great benefits, including a 401k match and 15 days PTO.

Qualifications

• 1+ years of experience in a medical setting, working with patients.
• Preference for Bachelor's degree.
• Experience in phlebotomy and EKG is preferred.

Responsibilities

• Assist in coordinating the research trial process with CRCs, Site Managers, and PIs.
• Educate patients about trials and benefits/risks of participation.
• Determine protocol-related needs and order supplies.
• Recruit and screen potential patients and obtain informed consent.
• Complete source documents to facilitate data collection.
• Conduct in-service programs to assist in protocol understanding.
• Schedule patient visits and diagnostic tests.
• Assist with investigational product shipments.
• Review patient progress and trends.
• Perform clinical skills as required by the protocol.

Skills

Patient interaction

Phlebotomy

EKG

Electronic medical data platforms

Education

Bachelor's degree

Job description

• Great benefits including 401k w/match and 15 days PTO
• Monday-Friday, 8:30 AM - 5 PM
• Great opportunity to get involved in clinical research!

About Our Client

Our client is a fast growing site network that currently has over 30 sites and constantly expanding! They focus on diversity in their trials including therapeutic areas: oncology, cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best-in-class experience for patients and sponsors.

Responsibilities

• Assist in coordinating the research trial process with CRCs, Site Managers, and PIs
• Assists in educating patients about the nature of the trials and the benefits and risks of participating
• Determine protocol-related needs to conduct the trial and order supplies and equipment
• Recruits and screens potential patients and obtains informed consent
• Completed 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
• Review trends, problems encountered, patient adverse events, and patient progress
• Perform other clinical skills as required by the trial protocol, including vital signs, ECGs and blood glucose testing

Qualifications

• 1+ years of experience in a medical setting, working with patients.
• Bachelor's degree preferred
• Phlebotomy and EKG experience preferred
• Familiar with using electronic platforms for medical data