Clinical Research Assistant

ZipRecruiter; St. Louis (MO); On-site; USD 40,000 - 55,000; Full time

Job summary

A leading company is seeking an experienced Clinical Research Assistant to support clinical trials. Responsibilities include data entry, patient recruitment, and coordination of clinical research activities. The ideal candidate will have strong administrative skills, attention to detail, and prior clinical research experience. This full-time position offers a competitive salary and benefits package.

Benefits

401K

Medical

Dental

Paid Time Off

Qualifications

• Prior clinical research experience preferred.
• Medical Assistant certification is a plus.

Responsibilities

• Complete accurate data entry into case report forms.
• Assist with patient recruitment and coordinate data collection.
• Communicate and coordinate with study personnel.

Skills

Attention to Detail

Customer Service

Communication

Self-motivated

Education

High school diploma or GED

Tools

Electronic Medical Records (EMR)

Job description

Job Description

We are seeking an experienced and enthusiastic Clinical Research Assistant to join our team! The Clinical Research Assistant will provide support for the Principal Investigator(s) and Clinical Research Coordinator(s) to streamline clinical trial conduct, ensuring quality data collection and patient care.

Essential Functions of the Role:

1. Complete accurate data entry into case report forms or pre-established computer formats, ensuring appropriate source documentation.
2. Transfer data from paper formats via computer, recorders, or scanners.
3. Screen patient records, EMR, and physician referral summaries to identify prospective candidates for research protocols.
4. Assist with patient recruitment.
5. Coordinate data collection according to the research protocol, operations manual, and case report form guidelines within the budgetary guidelines established by the Manager of Clinical Trial Operations and Principal Investigator.
6. Draw, prepare, and ship laboratory samples for clinical trials.
7. Perform EKGs and other procedures as directed by the study protocol and delegated by the Principal Investigator.
8. File various paperwork.
9. Organize spreadsheets with large amounts of data.
10. Maintain and update site demographics on the computer database; log forms received and file appropriately; prepare reports from the database, including weekly and other reports as requested.
11. Communicate and coordinate with other study personnel, including data entry, randomization, pharmacy, laboratories, study sponsors, and others as needed for study implementation and routine problem resolution.
12. Attend routine meetings and other meetings related to clinical research; stay informed of any changes to the study protocol.

Other duties as assigned.

Minimum Qualifications:

• High school diploma or GED required.
• Prior clinical research experience preferred.
• Medical Assistant certification is a plus; familiarity with medical terminology is advantageous.
• Proficient computer skills, especially with electronic medical records (EMR).
• Strong administrative skills, with attention to detail in data recording.
• Excellent customer service skills.
• Attentiveness to detail and keen observation skills.
• Ability to manage and coordinate multiple stakeholders.
• Excellent oral and written communication skills.
• Self-motivated and able to work independently and as part of a team.

Work Environment

This position reports to the office Monday through Friday, from 6:30 am to 5:00 pm, or other hours as needed to support business requirements.

Physical Requirements

This role requires full body motion: sitting, walking, standing, speaking, hearing, repetitive hand movements, reaching, and lifting up to 25 pounds.

Equal Employment Opportunity Statement

We are committed to providing equal employment opportunities to all employees and applicants, prohibiting discrimination and harassment of any kind based on protected characteristics. This policy covers all aspects of employment, including recruitment, hiring, promotion, termination, and benefits.

Salary and Benefits

This is a full-time, non-exempt position with a competitive salary and benefits package, including 401K, medical, dental, ancillary benefits, paid time off, and more.

The above description is intended to outline the general responsibilities and requirements for the role but is not exhaustive. Other duties may be assigned as needed, and accommodations may be provided for qualified individuals with disabilities.