Job Title: Clinical Research Coordinator
Job Description

The Clinical Research Coordinator is responsible for managing complex clinical trials in accordance with FDA and GCP guidelines. This position supports both the Glaucoma Research Center (ACORN Lab) and the Vision Research Center.

ResponsibilitiesCollaborate closely with the study team to identify problems and develop solutions.Coordinate study activities for IIT studies, multi-center research studies, and patient-oriented clinical and translational research projects.Ensure compliance with regulatory protocols.Screen patients for eligibility, enroll and monitor study patients in an outpatient setting, and ensure protocol compliance.Perform ophthalmic photography and diagnostic services.Collect, review, and report study data to sponsors and resolve data discrepancies.Essential SkillsBachelor's Degree4-5 years of experience as a Clinical Research CoordinatorKnowledge of FDA and IRB requirements for drug and device protocolsExperience in clinical research, clinical trials, patient recruitment, GCP, and chart reviewAdditional Skills & QualificationsOphthalmic experience strongly preferredKnowledge of regulatory, IRB, and data entry processesPhlebotomy skillsCCRP or CRA certification strongly preferredKnowledge of human research protection regulationsFlexibility to work on different studiesWork Environment

This is a full-time, on-site position located in Philadelphia. The standard work hours are 9-5, although some hours may vary depending on patient schedules. This role involves direct patient interaction and offers the opportunity to work with state-of-the-art diagnostic and imaging tools for eyes.

Pay and Benefits

The pay range for this position is $27.00 - $32.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Philadelphia,PA.

Application Deadline

This position is anticipated to close on Mar 14, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.