Clinical Research Technician- Oph

Tufts Medical Center; Boston, Evanston Township (MA, IL); On-site; USD 40,000 - 80,000; Full time

Job summary

An established industry player seeks a motivated individual to join their clinical research team. This role involves assisting in planning and implementing clinical studies, working closely with patients and their families. You will coordinate trial activities, manage compliance, and ensure the highest standards of patient care. If you have a passion for research and a commitment to improving patient outcomes, this opportunity is perfect for you. Join a diverse and inclusive environment where your contributions will make a significant impact in the field of medicine.

Qualifications

• Minimum of two years experience in research-related activities.
• High school diploma or equivalent required, Bachelor's preferred.

Responsibilities

• Assist in recruitment and screening of study participants.
• Coordinate clinical trial activities and manage compliance.
• Maintain patient confidentiality and secure study information.

Skills

Interpersonal Skills

Communication Skills

Organizational Skills

Data Collection and Analysis

Knowledge of Anatomy and Physiology

Proficiency in Computer Skills

Adaptability

Education

High School Diploma

Bachelor's Degree in a Research-Related Field

Job description

Job Profile Summary

This role focuses on research and development of new products, innovation, and process improvement. It involves supporting the development of new products, clinical research projects, and basic, translational, or clinical research aimed at solving specific problems for an entity or community. The role also includes organizational support or service roles that operate in a 'hands-on' environment, primarily delivering support services or activities under supervision. It requires basic knowledge of job procedures and tools, obtained through work experience or vocational/technical education, and involves routine problem-solving and communication.

Job Overview

This position assists in planning and implementing clinical research studies, working directly with patients and their families, providing advanced imaging, and facilitating all phases of new studies. It involves coordinating clinical trial activities, aiding Principal Investigators in patient recruitment, and managing compliance, financial, and personnel aspects of ongoing studies.

Job Description

Minimum Qualifications:

• High school diploma or equivalent.
• Two (2) years of experience in research-related activities.

Preferred Qualifications:

• Bachelor's degree in a research-related field.
• Five (5) years of experience in research-related activities.

Duties and Responsibilities:

1. Assist in recruitment and screening of study participants.
2. Coordinate and conduct follow-up with participants.
3. Complete source document abstraction and study forms.
4. Ensure compliance with policies and regulations protecting human subjects.
5. Review protocols with the clinical team and ensure understanding of roles.
6. Assist with IRB requirements, document submissions, and adverse event reporting.
7. Maintain patient confidentiality and secure study information.
8. Identify and resolve protocol compliance issues.
9. Arrange tests and procedures as per protocol, report results.
10. Participate in site visits, maintain study supplies and equipment certifications.
11. Monitor adverse events, report to investigators and sponsors.
12. Assess patient eligibility, review records, and verify information with physicians.
13. Interview patients, obtain informed consents, and maintain study documentation.

Physical Requirements:

• Assist patients physically, including helping with mobility and escorting.
• Prolonged standing, walking, bending, and stretching.
• Close contact with diverse patient populations, some exposure to blood and needles.

Skills & Abilities:

• Excellent interpersonal and communication skills.
• Ability to work effectively with clinical staff and patients.
• Knowledge of anatomy, physiology, and biological sciences.
• Organizational, data collection, and analysis skills.
• Proficiency in computer and graphic skills.
• Ability to prioritize and work efficiently in a fast-paced environment.
• Knowledge of patient care across different age groups.
• Self-motivated, energetic, detail-oriented, and adaptable.

Tufts Medicine is committed to diversity and inclusion and provides reasonable accommodations for applicants with disabilities. Contact us at [e-mail] for assistance.