Research Coordinator

About the role

Support clinical research studies by coordinating participant recruitment, screening, scheduling, and study visits.
Assist physicians and research nurses in delivering high-quality patient care while ensuring compliance with study protocols, FDA regulations, and Good Clinical Practice (GCP) standards.
Manage study documentation, data collection, laboratory processes, and communication with sponsors, investigators, and regulatory agencies.
Play a key role in maintaining participant safety and contributing to the successful completion of clinical trials.

Responsibilities

• Recruit and engage study participants through community outreach, physician referrals, and screening efforts.
• Accurately and timely collect, document, and report study data, adverse events, and regulatory requirements.
• Cook up participant visits and maintain ongoing communication to promote a positive study experience and strong retention.
• Coordinate with sponsors, investigators, and regulatory agencies to ensure compliance with study protocols and regulations.
• Help advance medical research by contributing to the successful execution and completion of clinical trials.

Requirements

• High School Diploma required.
• Certified Medical Assistant (CMA) certification required.
• Clinical research experience preferred, with an understanding of study coordination, documentation, and regulatory requirements.
• Current Basic Life Support (BLS) certification.
• Strong organizational skills with the ability to manage multiple priorities and maintain detailed records.
• Excellent communication and interpersonal skills, with a commitment to patient care and participant safety.
• Team-oriented mindset with a willingness to learn, collaborate, and support colleagues in a fast-paced clinical environment.
• Ability to maintain accuracy, confidentiality, and compliance with FDA, OSHA, and study-specific guidelines.

Qualifications

• High School Diploma required.
• Certified Medical Assistant (CMA) certification required.
• Clinical research experience preferred.
• Current Basic Life Support (BLS) certification.
• Strong organizational skills.
• Excellent communication and interpersonal skills.
• Team-oriented mindset.
• Ability to maintain accuracy, confidentiality, and compliance.

Skills

• Study coordination.
• Data collection.
• Regulatory compliance.
• Participant safety.
• Medical research.

Benefits

• Choice of three health insurance plans.
• Dental insurance coverage.
• Vision insurance coverage.
• 401(k) with company match and profit-sharing plan.
• Company-paid short-term and long-term disability coverage.
• Company-paid life insurance for you and your family.
• Access to company-provided training and educational resources.
• Annual merit-based performance increases.
• Accrued General Purpose Time (GPT).
• Eight company-paid holidays.
• Special company events, including Christmas parties, Family Day, employee engagement activities, and Spirit Days.
• Complimentary Employee Assistance Program (EAP) for all employees and their dependents.

Pay

TBD

Schedule

TBD