Clinical Research Screener

POSITION OVERVIEW

We are seeking a highly motivated and detail-oriented Clinical Research Screener to join our dynamic research team. The Clinical Research Screener will play a crucial role in the initial screening process for potential participants in clinical trials. This position involves assessing eligibility criteria, conducting initial interviews, and collecting relevant information to determine participant suitability for specific research studies. The successful candidate will work closely with the research team to ensure the efficient and accurate identification of eligible candidates, contributing to the advancement of cutting-edge medical research.

RESPONSIBILITIES

• Participant Screening: Review and assess potential participants for clinical trials based on established eligibility criteria.
• Documentation: Maintain accurate and detailed records of participant screenings, ensuring compliance with regulatory and ethical standards.
• Communication: Collaborate effectively with the research team to communicate participant eligibility and relevant information, fostering a seamless transition from screening to enrollment.
• Data Entry: Enter screening data into electronic databases, ensuring accuracy and completeness of information.
• Adherence to Protocols: Ensure strict adherence to study protocols and regulatory guidelines during the screening process.
• Continuous Learning: Stay informed about relevant research protocols, therapeutic areas, and industry standards to enhance screening effectiveness.

QUALIFICATIONS

Qualifications:

• Education: Bachelor's degree in a relevant field (e.g., life sciences, nursing, psychology). Foreign MD preferred.
• Experience: Previous experience in clinical research, patient recruitment, or a related field is preferred.
• Communication Skills: Strong interpersonal and communication skills, with the ability to convey complex information in a clear and understandable manner.
• Detail-Oriented: Exceptional attention to detail and organizational skills to maintain accurate and comprehensive records.
• Ethical Standards: Understanding of ethical principles in clinical research and commitment to participant safety and confidentiality.
• Team Player: Ability to work collaboratively in a multidisciplinary team environment.
• Computer Skills: Proficiency in Microsoft Office and familiarity with electronic data capture systems.

Please note that this job description is not exhaustive, and additional responsibilities may be assigned as needed.

Job Type: Full-time

Pay: From $25.00 per hour

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Education:

• High school or equivalent (Preferred)

Experience:

• clinical screening: 1 year (Preferred)

Ability to Commute:

• Los Alamitos, CA (Preferred)

Work Location: In person