Norfolk, VA - Clinical Research Coordinator

Job Title: Clinical Research Coordinator – Norfolk, VA

Start Date: ASAP

Job Description

This role provides experienced clinical research coordination support for an cardiology clinical trial at a research site in Norfolk, VA. The Clinical Research Coordinator will focus on accurate electronic data capture, timely query resolution, and clear communication about the clinical trial while working closely with the site team. The position is a 40 hour a week contract role.

Responsibilities

• Collect and enter clinical trial data accurately and promptly into the electronic data capture (EDC) system.

• Review source documents and patient charts to ensure data completeness, accuracy, and consistency with protocol requirements.

• Identify, investigate, and resolve data queries in the EDC system in a timely manner.

• Communicate clearly about the clinical trial with patients and site staff, ensuring information is accurate and appropriate.

• Perform detailed chart reviews to verify data and support high-quality documentation.

• Collaborate with the site research team to maintain compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.

• Maintain meticulous records and documentation to support monitoring visits, audits, and inspections.

• Prioritize tasks effectively in a fast-paced environment to meet study timelines and data entry deadlines.

Essential Skills

• Proven experience as a Clinical Research Coordinator.

• At least 2 years of experience with electronic data capture (EDC) data entry.

• Hands-on experience working on cardiology clinical trials.

• Proficiency with EDC systems and electronic medical records (EMR).

• Strong attention to detail and accuracy in data entry and documentation.

• Ability to interpret and review patient charts and clinical documentation.

• Effective communication skills for interacting with patients and clinical research staff.

• Ability to work both independently and as part of a research team in a fast-paced setting.

Additional Skills & Qualifications

• Prior experience coordinating cardiology studies at a clinical research site.

• Comfort working with multiple clinical systems, including EMR and EDC platforms.

• Strong organizational skills to manage multiple tasks and data timelines.

• Ability to adapt to changing study needs and priorities.

Work Environment

The role follows normal business hours in a fast-paced clinical research setting. The position is onsite, with an expectation to work onsite 5 days per week. The environment requires consistent attention to detail, frequent use of electronic medical record (EMR) and electronic data capture (EDC) systems, and regular collaboration with clinical and research staff. The coordinator will work in a professional clinical office environment that supports focused, accurate data entry and documentation.

Job Type & Location

This is a Contract position based out of Norfolk, VA.

Pay and Benefits

The pay range for this position is $25.00 - $35.00/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 Norfolk,VA.

Application Deadline

This position is anticipated to close on Jun 16, 2026.

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.

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 View email address on click.appcast.io for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

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