Clinical Research Assistant - Level 1 CRC

Supports the research team in conducting clinical trials by recruiting study participants, collecting and managing data, ensuring protocol adherence, and assisting with administrative tasks under the supervision of a principal investigator (PI) while adhering to ethical and regulatory guidelines.

Responsibilities

• Collect and authenticate data collection forms (case report forms).
• Work closely with Clinical Research Coordinators (CRCs), Principal Investigators (PIs), and site staff to complete trials successfully.
• Screen potential study participants through medical record reviews.
• Maintain specific records of research activity, including regulatory forms, drug dispensation records, case reports, and consent forms.
• Ensure proper transmission of clinical case data to data management centers; review case report questions and problems, and clarify or obtain alterations to data as appropriate.
• Process, label, and ship study samples.
• Ensure lab supplies, sample kits, and all study binders are properly maintained.
• Support CRCs to prepare for study visits and monitoring visits.
• Perform vital signs, EKG, phlebotomy, and other study procedures as needed.
• Other duties as assigned.

Requirements

• 2 years’ related experience with a High School Diploma or 1 year experience with an Associate's Degree.
• 0–3 years of experience in clinical research or a related area.
• Clear understanding of FDA regulatory requirements and clinical research protocols.
• Familiarity with commonly used concepts, practices, and procedures in the field.
• Ability to follow detailed instructions and predefined guidelines.
• Excellent communication and interpersonal skills.
• Strong attention to detail and meticulous work habits.
• Responsible, punctual, and able to maintain confidentiality.

Benefits

• 401(k) matching
• Bonus based on performance
• Competitive salary
• Dental insurance
• Health insurance
• Opportunity for advancement
• Paid time off
• Tuition assistance