Part Time Clinical Research Coordinator

Job Title: Part Time Clinical Research Coordinator (Hybrid)

Job Description

This contract position offers an opportunity for an experienced Clinical Research Coordinator to support an ongoing clinical trial at a research site in El Paso, TX. The coordinator will ensure accurate electronic data capture, timely query resolution, and clear communication with patients and site staff while working closely with the research team. This role will only require candidates within a commutable distance of El Paso, TX.

Responsibilities

• Collect and enter clinical trial data accurately and promptly into electronic data capture systems.
• Review source documents and patient charts to confirm data completeness, accuracy, and consistency with protocol requirements.
• Identify, investigate, and resolve data queries in electronic data capture systems in a timely manner.
• Communicate clearly and professionally about the clinical trial with patients and site staff, ensuring information is accurate, understandable, 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 applicable 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.
• Use electronic medical records and other clinical systems to support accurate data collection and documentation.
• Support the cardiology study team by coordinating day-to-day trial activities as needed.

Essential Skills

• Proven experience as a Clinical Research Coordinator.
• At least 2 years of experience with electronic data capture data entry.
• Hands-on experience working on cardiology clinical trials.
• Proficiency with electronic data capture 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.
• Experience in query resolution within clinical trial data systems.
• Training in HIPAA and Good Clinical Practice (GCP).

Additional Skills & Qualifications

• Prior experience coordinating cardiology studies at a clinical research site.
• Comfort working with multiple clinical systems, including EMR and electronic data capture platforms.
• Strong organizational skills to manage multiple tasks and data timelines.
• Ability to adapt to changing study needs and priorities.
• Experience working within a clinical trial environment that requires frequent query resolution and collaboration with cross-functional teams.

Job Type & Location This is a Contract position based out of El Paso, TX. 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 hybrid position in El Paso,TX. Application Deadline This position is anticipated to close on Jun 18, 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 [email protected] for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions Apply tot his job Apply To this Job