Clinical Research Coordinator

Erie Retina Research; Erie (Erie County); On-site; USD 50,000 - 70,000; Full time

Job summary

Erie Retina Research in Erie, PA seeks a Clinical Research Coordinator responsible for executing and overseeing ophthalmic clinical trials. The role involves ensuring protocol compliance, coordinating patient activities, and serving as a liaison between investigators, patients, sponsors, and CROs.

The ideal candidate should have an associate's or bachelor's degree in life sciences and at least two years of experience in clinical research. Strong communication skills and proficiency in EDC systems are preferred. This is an onsite role.

Qualifications

• 2+ years of clinical research or healthcare experience preferred.
• Experience coordinating clinical trials strongly preferred.
• Ophthalmology or specialty clinic experience is a plus.

Responsibilities

• Oversee daily execution of clinical trial activities.
• Ensure procedures comply with study protocols.
• Monitor and report adverse events.

Skills

Knowledge of clinical research processes

Strong organizational skills

Effective communication

Multitasking abilities

Proficiency with EDC systems

Education

Associate’s or Bachelor’s degree in Life Sciences or related field

Tools

Microsoft Office tools

Job description

Erie Retina Research is a subsidiary of Lexitas Pharma Services.

Spearheaded by Dr David Almeida, MD, MBA, PhD, Erie Retina Research offers cutting edge surgical and pharmaceutical ophthalmic research. Our team is fast paced, energetic, innovative and proud of our groundbreaking work and practices in Erie, PA. We can help facilitate studies, bring products to market, collaborate on ophthalmology-related research, and more. We bring groundbreaking studies to our community and we are focused on vision and committed to empowering sight through science.

Overview

The Clinical Research Coordinator is a mission-critical role responsible for the execution and oversight of ophthalmic clinical trials. This position ensures protocol compliance, regulatory adherence, and seamless coordination of patient activities while maintaining the highest standards of care and operational efficiency.

The Clinical Research Coordinator serves as a central liaison between investigators, patients, sponsors, CROs, and internal teams, ensuring all trial-related procedures are conducted accurately, ethically, and in alignment with regulatory standards and site objectives.

Responsibilities

Operational Oversight & Protocol Adherence

• Oversee daily execution of clinical trial activities from site initiation through close-out.
• Ensure all procedures are conducted in accordance with study protocols and regulatory requirements.
• Prepare for and support sponsor monitoring visits, audits, and inspections.
• Maintain site readiness and compliance in collaboration with leadership.
• Recruit, screen, and enroll eligible patients, ensuring proper informed consent.
• Coordinate patient scheduling, diagnostic testing, and follow-up visits.
• Monitor and report adverse events with appropriate documentation.
• Deliver a high-quality patient experience to promote engagement and retention.

Regulatory & Sponsor Communication

• Serve as liaison with sponsors, CROs, and internal departments.
• Prepare and submit IRB documentation including amendments and renewals.

Cross-Functional Collaboration

• Partner with physicians, technicians, medical assistants, and administrative teams.
• Participate in investigator meetings, training, and team discussions.
• Support overall clinical and operational excellence in study execution.

Requirements

Education:

Associate’s or Bachelor’s degree in Life Sciences, Healthcare, or related field preferred

Experience:

• 2+ years of clinical research or healthcare experience preferred
• Experience coordinating clinical trials strongly preferred
• Ophthalmology or specialty clinic experience is a plus

Certifications:

• Clinical Research Coordinator (CRC), CCRA, or similar certification preferred but not required
• Good Clinical Practice (GCP) training required

Skills:

• Strong knowledge of clinical research processes and regulatory requirements
• Excellent organizational and multitasking abilities
• Strong attention to detail and documentation accuracy
• Effective communication and interpersonal skills
• Ability to coordinate across cross-functional teams
• Proficiency with EDC systems and Microsoft Office tools

*This is an onsite role in Erie, PA.

Physical Requirements

Position requires: ordinary ambulatory skills and physical coordination sufficient to move about conference or meeting locations as required; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of 10-35 pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time.

Disclaimer:

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. Lexitas Pharma Services, Inc., at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. Lexitas Pharma Services, Inc., at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.